Gene Details



FANCD2 and homologs in 5 species are found in 616 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier I Mouse MP 453 Genes GS170247: MP:0002038 carcinoma
Expand Tier I Human 17 Genes GS173775: HP:0005344 Abnormality of the carotid arteries
Expand Tier I Mouse GO 537 Genes GS180039: GO:0032504 multicellular organism reproduction
Expand Tier I Mouse MP 489 Genes GS166812: MP:0002209 decreased germ cell number
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Mouse MP 88 Genes GS167649: MP:0004201 fetal growth retardation
Expand Tier I Mouse GO 91 Genes GS184618: GO:0010212 response to ionizing radiation
Expand Tier I Mouse MP 3631 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse GO 997 Genes GS179428: GO:0022414 reproductive process
Expand Tier I Human 8 Genes GS170944: HP:0004742 Abnormality of the renal collecting system
Expand Tier I Human GO 157 Genes GS199987: GO:0051327 M phase of meiotic cell cycle
Expand Tier I Human 48 Genes GS171928: HP:0100577 Urinary bladder inflammation
Expand Tier I Mouse GO 1001 Genes GS191083: GO:0000003 reproduction
Expand Tier I Mouse MP 835 Genes GS167063: MP:0001929 abnormal gametogenesis
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human CTD 2780 Genes GS123332: 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide interacting genes (MeSH:D015123) in CTD
Expand Tier I Human 8 Genes GS171713: HP:0000792 Kidney malformation
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human GO 579 Genes GS195583: GO:0019953 sexual reproduction
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 18 Genes GS176340: HP:0001549 Abnormality of the ileum
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse GO 727 Genes GS179950: GO:0006259 DNA metabolic process
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier II Mouse 393 Genes GS84186: differences in cocaine responsiveness (Published QTL, Chr 6)
Expand Tier I Human 16 Genes GS173779: HP:0010293 Aplasia/Hypoplasia of the uvula
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 35 Genes GS175326: HP:0001217 Clubbing
Expand Tier I Mouse 360 Genes GS135843: femoral cross-sectional area 1 (Fcsa1, Published QTL Chr 6)
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 73 Genes GS171188: HP:0000415 Abnormality of the choanae
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 161 Genes GS199989: GO:0051321 meiotic cell cycle
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 21 Genes GS195331: GO:0007129 synapsis
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Mouse MP 80 Genes GS163604: MP:0004227 increased cellular sensitivity to ionizing radiation
Expand Tier I Mouse MP 103 Genes GS164349: MP:0010094 abnormal chromosome stability
Expand Tier I Mouse MP 102 Genes GS169763: MP:0008866 chromosomal instability
Expand Tier I Human 46 Genes GS171082: HP:0009601 Aplasia/Hypoplasia of the thumb
Expand Tier I Human 114 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Mouse 484 Genes GS135414: bronchial hyperresponsiveness 5 (Bhr5, Published QTL Chr 6)
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse MP 1172 Genes GS162953: MP:0002020 increased tumor incidence
Expand Tier I Human 68 Genes GS175207: HP:0000978 Bruising susceptibility
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Mouse MP 1082 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier I Mouse MP 16 Genes GS163480: MP:0004833 ovary atrophy
Expand Tier I Mouse GO 25 Genes GS178581: GO:0007129 synapsis
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 606 Genes GS191738: GO:0022403 cell cycle phase
Expand Tier I Human 72 Genes GS172350: HP:0000135 Hypogonadism
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 6 Genes GS174988: HP:0009943 Complete duplication of the phalanges of the thumb
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 848 Genes GS208675: GO:0022403 cell cycle phase
Expand Tier I Human GO 688 Genes GS193888: GO:0051276 chromosome organization
Expand Tier I Mouse MP 2357 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human 111 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Mouse MP 1038 Genes GS169114: MP:0004196 abnormal prenatal growth/weight/body size
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 78 Genes GS173155: HP:0005561 Abnormality of bone marrow cell morphology
Expand Tier I Mouse 530 Genes GS136830: TNF-induced lethal shock susceptibility 1 (Tilss1, Published QTL Chr 6)
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 501 Genes GS207582: GO:0007276 gamete generation
Expand Tier I Mouse 484 Genes GS135881: femur geometry 5 (Fmgty5, Published QTL Chr 6)
Expand Tier I Mouse 491 Genes GS136206: lung tumor shape-determining 8 (Ltsd8, Published QTL Chr 6)
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 223 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human 115 Genes GS170850: HP:0006265 Aplasia/Hypoplasia of fingers
Expand Tier I Human 85 Genes GS176626: HP:0001909 Leukemia
Expand Tier II Mouse 389 Genes GS84185: high-dose ethanol actions (Published QTL, Chr 6)
Expand Tier I Mouse 469 Genes GS135505: bulb size 2 (Bulb2, Published QTL Chr 6)
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse 477 Genes GS136051: IGF-1 serum levels 1 (Igf1sl1, Published QTL Chr 6)
Expand Tier I Human GO 806 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Human GO 1165 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse GO 537 Genes GS190817: GO:0048609 multicellular organismal reproductive process
Expand Tier II Mouse 371 Genes GS84184: METH responses for body temperature (Published QTL, Chr 6)
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse MP 227 Genes GS163627: MP:0001930 abnormal meiosis
Expand Tier I Mouse MP 1435 Genes GS168063: MP:0000313 abnormal cell death
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Mouse 405 Genes GS136367: obesity QTL 14 (Obq14, Published QTL Chr 6)
Expand Tier I Mouse MP 570 Genes GS164042: MP:0002018 malignant tumors
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Mouse GO 1123 Genes GS192256: GO:0007049 cell cycle
Expand Tier I Human 29 Genes GS176691: HP:0000104 Renal agenesis
Expand Tier I Human GO 637 Genes GS207720: GO:0048609 multicellular organismal reproductive process
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse 561 Genes GS136039: immediate cutaneous hypersensitivity QTL (Ichs, Published QTL Chr 6)
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 57 Genes GS171016: HP:0011893 Abnormal leukocyte count
Expand Tier I Human 6 Genes GS174873: HP:0001896 Reticulocytopenia
Expand Tier I Mouse MP 601 Genes GS167061: MP:0002210 abnormal sex determination
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human 19 Genes GS170994: HP:0000085 Horseshoe kidney
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier II Mouse 480 Genes GS84188: METH responses for home cage activity (Published QTL, Chr 6)
Expand Tier I Human 110 Genes GS172484: HP:0009997 Duplication of phalanx of hand
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse 539 Genes GS135895: gastritis type A susceptibility locus 3 (Gasa3, Published QTL Chr 6)
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Rat 742 Genes GS128047: Alcohol consumption QTL 14 (Alc14, Published QTL, Chr 4)
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 33 Genes GS171079: HP:0001882 Leukopenia
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse MP 532 Genes GS165820: MP:0001116 small gonad
Expand Tier I Mouse MP 1856 Genes GS165386: MP:0001262 decreased body weight
Expand Tier I Human 65 Genes GS171085: HP:0009602 Abnormality of the phalanges of the thumb
Expand Tier I Mouse MP 1966 Genes GS166590: MP:0002873 normal phenotype
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier I Human 18 Genes GS176476: HP:0009822 Aplasia involving forearm bones
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 1477 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 18 Genes GS172413: HP:0002245 Meckel diverticulum
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 48 Genes GS174811: HP:0001636 Tetralogy of Fallot
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human 98 Genes GS170997: HP:0000080 Abnormality of genital physiology
Expand Tier III Mouse 5726 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human 128 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Human 13 Genes GS175237: HP:0009777 Absent thumb
Expand Tier I Mouse MP 3437 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 41 Genes GS207853: GO:0010332 response to gamma radiation
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 537 Genes GS208127: GO:0000279 M phase
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Mouse GO 139 Genes GS183189: GO:0051327 M phase of meiotic cell cycle
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 104 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Mouse 513 Genes GS135945: HDL QTL 11 (Hdlq11, Published QTL Chr 6)
Expand Tier I Human 55 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Mouse MP 757 Genes GS163427: MP:0009205 abnormal internal male genitalia morphology
Expand Tier I Mouse MP 779 Genes GS163916: MP:0009198 abnormal male genitalia morphology
Expand Tier I Human 298 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse MP 4173 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 215 Genes GS166339: MP:0001131 abnormal ovarian follicle morphology
Expand Tier I Human 55 Genes GS174648: HP:0000957 Cafe-au-lait spot
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 93 Genes GS170972: HP:0001933 Subcutaneous hemorrhage
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 28 Genes GS175242: HP:0009778 Short thumb
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 96 Genes GS174884: HP:0009381 Short finger
Expand Tier I Mouse GO 30 Genes GS188222: GO:0070192 chromosome organization involved in meiosis
Expand Tier I Human GO 157 Genes GS195318: GO:0007126 meiosis
Expand Tier I Mouse MP 931 Genes GS163080: MP:0010273 increased classified tumor incidence
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse 561 Genes GS136384: obesity and body weight QTL 3 (Obwq3, Published QTL Chr 6)
Expand Tier I Human 24 Genes GS174728: HP:0100760 Clubbing of toes
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 31 Genes GS172259: HP:0001199 Triphalangeal thumb
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse 499 Genes GS136418: plasma apolipoprotein B (human) regulator 1 (Pabr1, Published QTL Chr 6)
Expand Tier I Mouse MP 1267 Genes GS164534: MP:0002019 abnormal tumor incidence
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse MP 60 Genes GS165344: MP:0006379 abnormal spermatocyte morphology
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse GO 416 Genes GS190683: GO:0007276 gamete generation
Expand Tier I Human 18 Genes GS172616: HP:0004312 Abnormality of reticulocytes
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse 531 Genes GS135570: cystic fibrosis body weight 2 (Cfbw2, Published QTL Chr 6)
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 12 Genes GS176182: HP:0000073 Ureteral duplication
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse MP 231 Genes GS162925: MP:0010383 increased adenoma incidence
Expand Tier I Mouse MP 1416 Genes GS164261: MP:0002081 perinatal lethality
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Mouse GO 480 Genes GS178827: GO:0019953 sexual reproduction
Expand Tier I Human 17 Genes GS174835: HP:0003974 Absent radius
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human 103 Genes GS173507: HP:0000520 Proptosis
Expand Tier I Mouse MP 250 Genes GS163015: MP:0002687 oligozoospermia
Expand Tier I Mouse 513 Genes GS136850: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 1 (Tmevd1, Published QTL Chr 6)
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 124 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human 101 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 30 Genes GS172414: HP:0002246 Abnormality of the duodenum
Expand Tier I Human 7 Genes GS170998: HP:0000081 Duplicated collecting system
Expand Tier I Mouse MP 220 Genes GS170240: MP:0001297 microphthalmia
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse MP 482 Genes GS167269: MP:0001147 small testis
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Mouse MP 325 Genes GS167066: MP:0002216 abnormal seminiferous tubule morphology
Expand Tier I Human GO 396 Genes GS208602: GO:0006281 DNA repair
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1317 Genes GS166711: MP:0002160 abnormal reproductive system morphology
Expand Tier I Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 71 Genes GS174898: HP:0100887 Abnormality of globe size
Expand Tier I Mouse MP 3110 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier I Mouse MP 661 Genes GS167367: MP:0002208 abnormal germ cell morphology
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Mouse MP 527 Genes GS170746: MP:0004849 abnormal testis size
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse 383 Genes GS136486: predicted fat percentage 2 (Pfat2, Published QTL Chr 6)
Expand Tier I Human 161 Genes GS171633: HP:0008373 Puberty and gonadal disorders
Expand Tier I Human 110 Genes GS173939: HP:0006101 Finger syndactyly
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Mouse MP 2485 Genes GS168012: MP:0010832 lethality during fetal growth through weaning
Expand Tier I Human CTD 85 Genes GS125044: Acetaldehyde interacting genes (MeSH:D000079) in CTD
Expand Tier I Human 145 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Mouse GO 621 Genes GS180679: GO:0009628 response to abiotic stimulus
Expand Tier I Human GO 166 Genes GS194416: GO:0000793 condensed chromosome
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse MP 1740 Genes GS166710: MP:0002163 abnormal gland morphology
Expand Tier I Human 139 Genes GS171000: HP:0000083 Renal insufficiency
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Rat 435 Genes GS128042: Alcohol consumption QTL 16 (Alc16, Published QTL, Chr 4)
Expand Tier I Mouse GO 571 Genes GS185937: GO:0005694 chromosome
Expand Tier I Mouse GO 883 Genes GS189820: GO:0044702 single organism reproductive process
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 11 Genes GS171741: HP:0003254 Abnormality of DNA repair
Expand Tier I Human 81 Genes GS175635: HP:0002251 Aganglionic megacolon
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Human 148 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Human CTD 26 Genes GS126895: Formaldehyde interacting genes (MeSH:D005557) in CTD
Expand Tier I Human 108 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Mouse MP 585 Genes GS169161: MP:0006362 abnormal male germ cell morphology
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 101 Genes GS171649: HP:0011849 Abnormal bone ossification
Expand Tier I Human 54 Genes GS172571: HP:0000340 Sloping forehead
Expand Tier I Mouse MP 165 Genes GS165045: MP:0004853 abnormal ovary size
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 14488 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 791 Genes GS191737: GO:0022402 cell cycle process
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 212 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 18 Genes GS175108: HP:0003953 Absent ossification/absent forearm bones
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 610 Genes GS177169: GO:0051276 chromosome organization
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse MP 521 Genes GS166636: MP:0001124 abnormal gametes
Expand Tier I Human 192 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Mouse 485 Genes GS135380: bone density traits 3 (Bdt3, Published QTL Chr 6)
Expand Tier I Human 54 Genes GS172298: HP:0001518 Small for gestational age
Expand Tier III Mouse 358 Genes GS216896: Co-expression cluster of haloperidol-induced catalepsy genes in striatum of HS mice short term selected lines. Turquoise Cluster
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier II Mouse 62 Genes GS26132: Positional candidate genes for Thermal Nociception Tail Withdrawal Test [Pain] in Females & Males for Significant BXD QTL on Chr6 from 112 to 116 Mb
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 52 Genes GS174291: HP:0002575 Tracheoesophageal fistula
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human 114 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human 59 Genes GS172412: HP:0002244 Abnormality of the small intestine
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 34 Genes GS176240: HP:0010932 Abnormality of nucleobase metabolism
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Mouse 509 Genes GS135628: collagen induced arthritis QTL 3 (Cia3, Published QTL Chr 6)
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 87 Genes GS173838: HP:0002778 Abnormality of the trachea
Expand Tier I Human 36 Genes GS173892: HP:0005528 Bone marrow hypocellularity
Expand Tier I Human 160 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human 26 Genes GS175175: HP:0003220 Abnormality of chromosome stability
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier III Mouse 3192 Genes GS213073: Genes with suggestive difference in (PB6F1) vs (B6PF1 + B6 + PWD) comparison
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 83 Genes GS171875: HP:0002997 Abnormality of the ulna
Expand Tier I Human 110 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Mouse 360 Genes GS136428: pulmonary adenoma susceptibility 1c (Pas1c, Published QTL Chr 6)
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human GO 319 Genes GS207688: GO:0009314 response to radiation
Expand Tier I Mouse MP 267 Genes GS169111: MP:0004197 abnormal fetal growth/weight/body size
Expand Tier I Human 4 Genes GS175385: HP:0003213 Deficient excision of UV-induced pyrimidine dimers in DNA
Expand Tier I Human 63 Genes GS175660: HP:0006501 Aplasia/Hypoplasia of the radius
Expand Tier I Human 81 Genes GS173031: HP:0004362 Abnormality of the enteric ganglia
Expand Tier I Mouse MP 1385 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 219 Genes GS167108: MP:0008942 abnormal induced cell death
Expand Tier I Human 69 Genes GS176623: HP:0000453 Choanal atresia
Expand Tier I Human GO 637 Genes GS196811: GO:0032504 multicellular organism reproduction
Expand Tier I Human GO 624 Genes GS202775: GO:0005694 chromosome
Expand Tier I Human GO 543 Genes GS200514: GO:0048610 cellular process involved in reproduction
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human GO 23 Genes GS205076: GO:0070192 chromosome organization involved in meiosis
Expand Tier I Mouse MP 316 Genes GS166634: MP:0001126 abnormal ovary morphology
Expand Tier I Mouse GO 144 Genes GS183191: GO:0051321 meiotic cell cycle
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse MP 2606 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 6 Genes GS172481: HP:0009998 Complete duplication of phalanx of hand
Expand Tier I Human 25 Genes GS176991: HP:0100867 Duodenal stenosis
Expand Tier I Mouse MP 68 Genes GS167556: MP:0009364 abnormal mature ovarian follicle morphology
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human 115 Genes GS171171: HP:0005607 Abnormality of the tracheobronchial system
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier II Mouse 62 Genes GS26131: Positional candidate genes for Thermal Nociception Tail Withdrawal Test [Pain] in Males for Significant BXD QTL on Chr6 from 112 to 116 Mb
Expand Tier I Mouse MP 238 Genes GS170688: MP:0002697 abnormal eye size
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Human 51 Genes GS171628: HP:0008053 Aplasia/Hypoplasia of the iris
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Mouse MP 451 Genes GS163418: MP:0009208 abnormal female genitalia morphology
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 111 Genes GS171465: HP:0004275 Duplication of hand bones
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Mouse MP 121 Genes GS166386: MP:0008871 abnormal ovarian follicle number
Expand Tier I Mouse GO 394 Genes GS183710: GO:0048610 cellular process involved in reproduction
Expand Tier I Human 43 Genes GS173130: HP:0001875 Neutropenia
Expand Tier II Mouse 428 Genes GS84187: high-dose ethanol actions (Published QTL, Chr 6)
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Mouse MP 455 Genes GS165816: MP:0001119 abnormal female reproductive system morphology
Expand Tier I Mouse MP 190 Genes GS166203: MP:0005169 abnormal male meiosis
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 229 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Mouse 475 Genes GS136656: skeletal muscle weight 15 (Skmw15, Published QTL Chr 6)
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 31 Genes GS174883: HP:0009380 Aplasia of the fingers
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 11 Genes GS170995: HP:0000086 Ectopic kidney
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human 67 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Mouse MP 1007 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human 114 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 37 Genes GS172691: HP:0100026 Arteriovenous malformation
Expand Tier I Human GO 1592 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human 80 Genes GS173498: HP:0001763 Pes planus
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse 500 Genes GS136278: modifier of ocular retardation 1 (Modor1, Published QTL Chr 6)
Expand Tier I Human 129 Genes GS173090: HP:0004377 Hematological neoplasm
Expand Tier I Mouse MP 779 Genes GS167267: MP:0001145 abnormal male reproductive system morphology
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 33 Genes GS173533: HP:0001876 Pancytopenia
Expand Tier I Human 42 Genes GS175750: HP:0000010 Recurrent urinary tract infections
Expand Tier I Mouse GO 28 Genes GS190945: GO:0010332 response to gamma radiation
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier II Mouse 129 Genes GS36754: Striatum Gene expression correlates of Vocalization Threshold - shock intensity (mA) in Females BXD
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Mouse 497 Genes GS136564: radiation pulmonary fibrosis 3 (Radpf3, Published QTL Chr 6)
Expand Tier I Human 19 Genes GS176709: HP:0100587 Abnormality of the preputium
Expand Tier I Rat 933 Genes GS128038: Alcohol consumption QTL 18 (Alc18, Published QTL, Chr 4)
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 451 Genes GS191213: GO:0000279 M phase
Expand Tier I Human CTD 52 Genes GS122104: chromium hexavalent ion interacting genes (MeSH:C074702) in CTD
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse GO 480 Genes GS185536: GO:0006974 response to DNA damage stimulus
Expand Tier I Mouse GO 139 Genes GS178565: GO:0007126 meiosis
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 56 Genes GS173053: HP:0000324 Facial asymmetry
Expand Tier I Human 58 Genes GS174923: HP:0008572 External ear malformation
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Mouse 484 Genes GS129105: bone mineral density 8 (Bmd8 Published QTL Chr 6)
Expand Tier I Human 4 Genes GS175600: HP:0011018 Abnormality of the cell cycle
Expand Tier I Human 136 Genes GS175524: HP:0000009 Functional abnormality of the bladder
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 4 Genes GS176763: HP:0001017 Anemic pallor
Expand Tier I Mouse MP 1476 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 43 Genes GS173577: HP:0011991 Abnormal neutrophil cell number
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier II Mouse 505 Genes GS84189: ethanol conditioned taste aversion (Published QTL, Chr 6)
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
Expand Tier I Human GO 1379 Genes GS209190: GO:0007049 cell cycle
Expand Tier I Human 52 Genes GS176559: HP:0000483 Astigmatism
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human GO 869 Genes GS196719: GO:0006259 DNA metabolic process
Expand Tier I Human 48 Genes GS174251: HP:0010161 Abnormality of the phalanges of the toes
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 14 Genes GS174987: HP:0009942 Duplication of phalanx of thumb
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 59 Genes GS171588: HP:0001562 Oligohydramnios
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 372 Genes GS135703: diabetes modifier 1 (Dbm1, Published QTL Chr 6)
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Mouse MP 5057 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Mouse MP 642 Genes GS167270: MP:0001146 abnormal testis morphology
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 111 Genes GS173651: HP:0009142 Duplication of bones involving the upper extremities
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 46 Genes GS170867: HP:0100736 Abnormality of the soft palate