Gene Details



PLOD1 and homologs in 1 species are found in 362 GeneSets:


- Entrez   - GeneNetwork   - 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 Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human GO 72 Genes GS198454: GO:0048029 monosaccharide binding
Expand Tier I Human GO 555 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Human GO 250 Genes GS201011: GO:0036293 response to decreased oxygen levels
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 1682 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 7 Genes GS175753: HP:0000015 Bladder diverticula
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 247 Genes GS200142: GO:0001666 response to hypoxia
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 280 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Human 9 Genes GS175318: HP:0000563 Keratoconus
Expand Tier I Human 37 Genes GS171851: HP:0000592 Blue sclerae
Expand Tier I Human GO 82 Genes GS209317: GO:0016702 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
Expand Tier I Human 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Human 201 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Human GO 18 Genes GS204136: GO:0009067 aspartate family amino acid biosynthetic process
Expand Tier I Human 17 Genes GS176999: HP:0001290 Generalized hypotonia
Expand Tier I Human 60 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 2921 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human GO 434 Genes GS202416: GO:0044711 single-organism biosynthetic process
Expand Tier I Human CTD 212 Genes GS124295: Polychlorinated Biphenyls interacting genes (MeSH:D011078) in CTD
Expand Tier I Human 33 Genes GS174067: HP:0002904 Hyperbilirubinemia
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human CTD 2422 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 61 Genes GS208235: GO:0008652 cellular amino acid biosynthetic process
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 56 Genes GS175070: HP:0000973 Cutis laxa
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 38 Genes GS171381: HP:0001558 Decreased fetal movement
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 565 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Human GO 211 Genes GS195507: GO:0043062 extracellular structure organization
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Human GO 3 Genes GS197428: GO:0008475 procollagen-lysine 5-dioxygenase activity
Expand Tier I Human 372 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 197 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human 129 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 52 Genes GS174808: HP:0001633 Abnormality of the mitral valve
Expand Tier I Human 55 Genes GS174818: HP:0007495 Prematurely aged appearance
Expand Tier I Human 30 Genes GS176144: HP:0001787 Abnormal delivery
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 147 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 58 Genes GS171388: HP:0001557 Prenatal movement abnormality
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 259 Genes GS195145: GO:0016053 organic acid biosynthetic process
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 243 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier I Human 43 Genes GS173159: HP:0002239 Gastrointestinal hemorrhage
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 80 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 140 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 2 Genes GS176961: HP:0001020 Soft, thin skin
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human GO 2455 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 112 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier I Human 44 Genes GS172038: HP:0000963 Thin skin
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 60 Genes GS171207: HP:0000098 Tall stature
Expand Tier I Human 9 Genes GS172309: HP:0100692 Increased corneal curvature
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 88 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier I Human 72 Genes GS175808: HP:0011028 Abnormality of blood circulation
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human GO 1 Genes GS197085: GO:0046946 hydroxylysine metabolic process
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 768 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 50 Genes GS175148: HP:0010511 Long toe
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 161 Genes GS202464: GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 68 Genes GS175207: HP:0000978 Bruising susceptibility
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human 174 Genes GS171806: HP:0005656 Positional foot deformities
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 259 Genes GS200383: GO:0046394 carboxylic acid biosynthetic process
Expand Tier I Human GO 845 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human 65 Genes GS175131: HP:0000023 Inguinal hernia
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 952 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 167 Genes GS197078: GO:0005506 iron ion binding
Expand Tier I Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Tier I Human 86 Genes GS172871: HP:0010490 Abnormality of the palmar creases
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 101 Genes GS171997: HP:0001762 Talipes equinovarus
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human CTD 48 Genes GS123568: 4-hydroxy-equilenin interacting genes (MeSH:C065250) in CTD
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human GO 856 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 147 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Human 41 Genes GS176789: HP:0100872 Abnormality of the plantar skin of foot
Expand Tier I Human GO 1276 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 80 Genes GS172248: HP:0001373 Joint dislocation
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human GO 453 Genes GS194627: GO:0008544 epidermis development
Expand Tier I Human 21 Genes GS175469: HP:0001176 Large hands
Expand Tier I Human 43 Genes GS171854: HP:0000591 Abnormality of the sclera
Expand Tier I Human GO 970 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
Expand Tier I Human GO 804 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 286 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 9 Genes GS176415: HP:0100678 Premature skin wrinkling
Expand Tier I Human 28 Genes GS172164: HP:0001182 Tapered finger
Expand Tier I Human 76 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Human 6 Genes GS175482: HP:0000993 Molluscoid pseudotumors
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 72 Genes GS175809: HP:0011029 Internal hemorrhage
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1762 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 14 Genes GS175066: HP:0000977 Soft skin
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 228 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 47 Genes GS207879: GO:0016706 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors
Expand Tier I Human 37 Genes GS176719: HP:0000541 Retinal detachment
Expand Tier I Human 101 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human GO 4 Genes GS196952: GO:0070815 peptidyl-lysine 5-dioxygenase activity
Expand Tier I Human 155 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 47 Genes GS175737: HP:0001238 Slender finger
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 66 Genes GS172844: HP:0000482 Microcornea
Expand Tier I Human GO 35 Genes GS204137: GO:0009066 aspartate family amino acid metabolic process
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 1 Genes GS174090: HP:0008458 Progressive congenital scoliosis
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human CTD 1122 Genes GS127166: bisphenol A interacting genes (MeSH:C006780) in CTD
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Human 80 Genes GS173498: HP:0001763 Pes planus
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human 5 Genes GS170923: HP:0005294 Arterial dissection
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 197 Genes GS204383: GO:0006575 cellular modified amino acid metabolic process
Expand Tier I Human 74 Genes GS174446: HP:0001120 Abnormality of corneal size
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 310 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 38 Genes GS174374: HP:0005922 Abnormal hand morphology
Expand Tier I Human 194 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 15 Genes GS175044: HP:0006532 Recurrent pneumonia
Expand Tier I Human GO 186 Genes GS200970: GO:0031406 carboxylic acid binding
Expand Tier I Human 257 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 2549 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 10 Genes GS172435: HP:0002647 Aortic dissection
Expand Tier I Human 31 Genes GS175063: HP:0000974 Hyperextensible skin
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 280 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 646 Genes GS204631: GO:1901566 organonitrogen compound biosynthetic process
Expand Tier I Human GO 210 Genes GS208505: GO:0030198 extracellular matrix organization
Expand Tier I Human 33 Genes GS174652: HP:0001131 Corneal dystrophy
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 4 Genes GS171676: HP:0003834 Shoulder dislocation
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 26 Genes GS176727: HP:0003043 Abnormality of the shoulder
Expand Tier I Human GO 21 Genes GS205315: GO:0031418 L-ascorbic acid binding
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 52 Genes GS174719: HP:0000774 Narrow chest
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human CTD 183 Genes GS125960: Cholecalciferol interacting genes (MeSH:D002762) in CTD
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 84 Genes GS202664: GO:0051213 dioxygenase activity
Expand Tier I Human 51 Genes GS174123: HP:0100807 Long fingers
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 94 Genes GS176573: HP:0008065 Aplasia/Hypoplasia of the skin
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human GO 83 Genes GS209319: GO:0016701 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen
Expand Tier I Human 144 Genes GS175754: HP:0000014 Abnormality of the bladder
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Human 4 Genes GS171715: HP:0007392 Excessive wrinkled skin
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 34 Genes GS172848: HP:0000488 Retinopathy
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 24 Genes GS176256: HP:0002783 Recurrent lower respiratory tract infections
Expand Tier I Human 35 Genes GS176775: HP:0001004 Lymphedema
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 4 Genes GS171762: HP:0007517 Palmoplantar cutis laxa
Expand Tier I Human GO 47 Genes GS203663: GO:0005791 rough endoplasmic reticulum
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 127 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Human 3 Genes GS174321: HP:0010303 Abnormality of the spinal meninges
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 422 Genes GS207919: GO:0044283 small molecule biosynthetic process
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human GO 706 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human GO 265 Genes GS197236: GO:0070482 response to oxygen levels
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 73 Genes GS176571: HP:0008067 Abnormally lax or hyperextensible skin
Expand Tier I Human 54 Genes GS171548: HP:0001388 Joint laxity
Expand Tier I Human 7 Genes GS176140: HP:0001788 Premature rupture of membranes
Expand Tier I Human GO 54 Genes GS194084: GO:0042398 cellular modified amino acid biosynthetic process
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 238 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 915 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human CTD 1001 Genes GS124711: Genistein interacting genes (MeSH:D019833) in CTD
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 137 Genes GS205251: GO:0019842 vitamin binding
Expand Tier I Human 41 Genes GS173096: HP:0000678 Dental crowding
Expand Tier I Human 29 Genes GS170949: HP:0005616 Accelerated skeletal maturation
Expand Tier I Human 87 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human GO 785 Genes GS204928: GO:0042175 nuclear outer membrane-endoplasmic reticulum membrane network
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 1 Genes GS197083: GO:0046947 hydroxylysine biosynthetic process
Expand Tier I Human CTD 798 Genes GS125548: Doxorubicin interacting genes (MeSH:D004317) in CTD
Expand Tier I Human 42 Genes GS175822: HP:0002090 Pneumonia
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human CTD 747 Genes GS125403: Diethylstilbestrol interacting genes (MeSH:D004054) in CTD
Expand Tier I Human 3 Genes GS173945: HP:0005952 Decreased pulmonary function
Expand Tier I Human 93 Genes GS170972: HP:0001933 Subcutaneous hemorrhage
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human CTD 307 Genes GS123854: Cyclophosphamide interacting genes (MeSH:D003520) in CTD
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 59 Genes GS172311: HP:0100691 Abnormality of the curvature of the cornea
Expand Tier I Human GO 16 Genes GS198488: GO:0030867 rough endoplasmic reticulum membrane
Expand Tier I Human 13 Genes GS172297: HP:0001519 Disproportionate tall stature
Expand Tier I Human GO 966 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Human 102 Genes GS173545: HP:0010647 Abnormal elasticity of skin
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 4 Genes GS174592: HP:0007605 Excessive wrinkling of palmar skin
Expand Tier I Human 75 Genes GS176150: HP:0003019 Abnormality of the wrist
Expand Tier I Human 62 Genes GS173367: HP:0005257 Thoracic hypoplasia
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 46 Genes GS175267: HP:0001166 Arachnodactyly
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 53 Genes GS174451: HP:0006705 Abnormality of the atrioventricular valves
Expand Tier I Human 249 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human 3 Genes GS174157: HP:0100775 Dural ectasia
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 267 Genes GS196679: GO:0030246 carbohydrate binding
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges