Gene Details



SDHD and homologs in 1 species are found in 385 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 GO 741 Genes GS201250: GO:0044429 mitochondrial part
Expand Tier I Human GO 52 Genes GS210158: GO:0006084 acetyl-CoA metabolic process
Expand Human 1321 Genes GS219728: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Human 1321 Genes GS219978: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human GO 381 Genes GS196559: GO:0019866 organelle inner membrane
Expand Tier I Human GO 556 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Human 1661 Genes GS219955: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Human 968 Genes GS219719: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human CTD 388 Genes GS121370: Clofibrate interacting genes (MeSH:D002994) in CTD
Expand Tier I Human 71 Genes GS170917: HP:0100852 Abnormal fear/anxiety-related behavior
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 12 Genes GS171599: HP:0001962 Palpitations
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 96 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 54 Genes GS176464: HP:0100242 Sarcoma
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 139 Genes GS194657: GO:0046906 tetrapyrrole binding
Expand Human 1339 Genes GS219979: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 2 Genes GS175572: HP:0002886 Vagal paraganglioma
Expand Tier I Human 51 Genes GS176092: HP:0100006 Neoplasm of the central nervous system
Expand Tier I Human 2 Genes GS171927: HP:0100570 Carcinoid
Expand Tier I Human CTD 917 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 6 Genes GS177042: HP:0001920 Renal artery stenosis
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human GO 27 Genes GS209846: GO:0046356 acetyl-CoA catabolic process
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 159 Genes GS208404: GO:0045333 cellular respiration
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Human 1661 Genes GS219981: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human GO 39 Genes GS194433: GO:0051187 cofactor catabolic process
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 11 Genes GS172027: HP:0000360 Tinnitus
Expand Tier I Human GO 328 Genes GS208795: GO:0015980 energy derivation by oxidation of organic compounds
Expand Human 1985 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human CTD 374 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Human 6 Genes GS176496: HP:0100780 Conjunctival hamartomas
Expand Tier I Human GO 55 Genes GS194047: GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Human 3 Genes GS174664: HP:0006737 Extraadrenal pheochromocytoma
Expand Tier I Human 16 Genes GS176091: HP:0100007 Neoplasm of the peripheral nervous system
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human 20 Genes GS173952: HP:0000853 Goiter
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human GO 44 Genes GS204135: GO:0009060 aerobic respiration
Expand Human 1149 Genes GS219976: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human GO 4 Genes GS201556: GO:0000104 succinate dehydrogenase activity
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 58 Genes GS196468: GO:0042775 mitochondrial ATP synthesis coupled electron transport
Expand Tier I Human GO 3 Genes GS202367: GO:0048039 ubiquinone binding
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Human GO 2 Genes GS210660: GO:0006121 mitochondrial electron transport, succinate to ubiquinone
Expand Tier I Human 53 Genes GS171415: HP:0000138 Ovarian cysts
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human 58 Genes GS173335: HP:0004363 Abnormality of calcium homeostasis
Expand Tier I Human 15 Genes GS174950: HP:0200043 Verrucae
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 12 Genes GS174198: HP:0009720 Adenoma sebaceum
Expand Tier I Human GO 819 Genes GS198970: GO:0031967 organelle envelope
Expand Tier I Human 43 Genes GS173159: HP:0002239 Gastrointestinal hemorrhage
Expand Tier I Human 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Human 1985 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 45 Genes GS170836: HP:0011772 Abnormality of thyroid morphology
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human GO 157 Genes GS207864: GO:0009055 electron carrier activity
Expand Tier I Human 7 Genes GS174607: HP:0001605 Vocal cord paralysis
Expand Tier I Human 3 Genes GS173929: HP:0001676 Palpitations (with pheochromocytoma)
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 46 Genes GS176540: HP:0002721 Immunodeficiency
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Human 1985 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 107 Genes GS176569: HP:0008069 Neoplasm of the skin
Expand Tier I Human GO 69 Genes GS198579: GO:0006119 oxidative phosphorylation
Expand Tier I Human 73 Genes GS171209: HP:0000093 Proteinuria
Expand Tier I Human 52 Genes GS173419: HP:0000147 Polycystic ovaries
Expand Tier I Human 103 Genes GS176735: HP:0010929 Abnormality of cation homeostasis
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Human 177 Genes GS222836: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_TRANSMISSION_ACROSS_CHEMICAL_SYNAPSES
Expand Tier I Human CTD 281 Genes GS125104: Ethionine interacting genes (MeSH:D005001) in CTD
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 33 Genes GS202498: GO:0009109 coenzyme catabolic process
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human 41 Genes GS171157: HP:0100742 Vascular neoplasm
Expand Tier I Human 72 Genes GS175808: HP:0011028 Abnormality of blood circulation
Expand Tier I Human 104 Genes GS171211: HP:0000091 Abnormality of the renal tubule
Expand Tier I Human 114 Genes GS172283: HP:0000820 Abnormality of the thyroid gland
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 3 Genes GS172058: HP:0002331 Headache (with pheochromocytoma)
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 23 Genes GS174001: HP:0010614 Fibroma
Expand Tier I Human GO 26 Genes GS199767: GO:0006099 tricarboxylic acid cycle
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Human 1417 Genes GS219977: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 13 Genes GS172519: HP:0001342 Cerebral hemorrhage
Expand Tier I Human 11 Genes GS172137: HP:0002858 Meningioma
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 28 Genes GS176196: HP:0004796 Gastrointestinal obstruction
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 I Human 66 Genes GS171279: HP:0100545 Arterial stenosis
Expand Tier I Human 9 Genes GS170983: HP:0100634 Neuroendocrine neoplasm
Expand Human 1661 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 5 Genes GS173569: HP:0003574 Positive regitine blocking test
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 100 Genes GS176774: HP:0001005 Dermatological manifestations of systemic disorders
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 4 Genes GS175616: HP:0008629 Pulsatile tinnitus
Expand Tier I Human 3 Genes GS173934: HP:0001673 Tachycardia (with pheochromocytoma)
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human GO 168 Genes GS197078: GO:0005506 iron ion binding
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human CTD 281 Genes GS121771: Benzbromarone interacting genes (MeSH:D001553) in CTD
Expand Tier I Human CTD 480 Genes GS122634: Ketone Bodies interacting genes (MeSH:D007657) in CTD
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 93 Genes GS174098: HP:0011792 Neoplasm by histology
Expand Tier I Human 87 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human 28 Genes GS173761: HP:0000519 Congenital cataract
Expand Tier I Human CTD 363 Genes GS125936: Tunicamycin interacting genes (MeSH:D014415) in CTD
Expand Tier I Human GO 2241 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human 14 Genes GS171923: HP:0100579 Mucosal telangiectasiae
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 2 Genes GS173191: HP:0012099 Abnormality of circulating catecholamine level
Expand Human 1339 Genes GS219948: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 12 Genes GS171550: HP:0001064 Diaphoresis
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 15 Genes GS171345: HP:0001048 Cavernous hemangioma
Expand Tier I Human 67 Genes GS173092: HP:0004375 Neoplasm of the nervous system
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 34 Genes GS173962: HP:0001581 Recurrent skin infections
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 4 Genes GS204477: GO:0045281 succinate dehydrogenase complex
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 1263 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human GO 110 Genes GS203056: GO:0022904 respiratory electron transport chain
Expand Tier I Human GO 4 Genes GS208854: GO:0045273 respiratory chain complex II
Expand Tier I Human 8 Genes GS171915: HP:0002666 Pheochromocytoma
Expand Tier I Human CTD 670 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Human 982 Genes GS219722: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Human GO 257 Genes GS194434: GO:0051186 cofactor metabolic process
Expand Human 1417 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 5 Genes GS173584: HP:0003345 Elevated urinary norepinephrine
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Human 1339 Genes GS219985: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 172 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 4 Genes GS176049: HP:0002377 Paraganglioma-related cranial nerve palsy
Expand Tier I Human GO 4034 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 57 Genes GS176765: HP:0001009 Telangiectasia
Expand Tier I Human 12 Genes GS172342: HP:0010615 Angiofibromas
Expand Tier I Human 6 Genes GS172429: HP:0002640 Hypertension associated with pheochromocytoma
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
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 I Human GO 69 Genes GS197357: GO:0005746 mitochondrial respiratory chain
Expand Human 1339 Genes GS219731: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 2 Genes GS174235: HP:0006715 Glomus tympanicum paraganglioma
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human GO 147 Genes GS197469: GO:0044455 mitochondrial membrane part
Expand Human 968 Genes GS219936: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 49 Genes GS173990: HP:0000502 Abnormality of the conjunctiva
Expand Tier I Human 77 Genes GS175999: HP:0100659 Abnormality of the cerebral vasculature
Expand Tier I Human 27 Genes GS175512: HP:0005214 Intestinal obstruction
Expand Tier I Human 72 Genes GS175809: HP:0011029 Internal hemorrhage
Expand Tier I Human GO 262 Genes GS202364: GO:0048037 cofactor binding
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 5 Genes GS173482: HP:0000875 Episodic hypertension
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 2 Genes GS173894: HP:0003334 Elevated circulating catecholamine level
Expand Tier I Human 29 Genes GS176913: HP:0002170 Intracranial hemorrhage
Expand Tier I Human 3 Genes GS171680: HP:0100642 Neoplasm of the adrenal medulla
Expand Tier I Human 20 Genes GS172391: HP:0000221 Furrowed tongue
Expand Tier I Human 151 Genes GS174920: HP:0000766 Abnormality of the sternum
Expand Tier I Human 22 Genes GS175941: HP:0100835 Benign neoplasm of the central nervous system
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 4 Genes GS198078: GO:0005749 mitochondrial respiratory chain complex II
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Human 968 Genes GS221018: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 93 Genes GS198220: GO:0006637 acyl-CoA metabolic process
Expand Human 968 Genes GS221267: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 39 Genes GS171701: HP:0100568 Neoplasm of the endocrine system
Expand Tier I Human GO 527 Genes GS198059: GO:0005740 mitochondrial envelope
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Human 1149 Genes GS219982: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 67 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 97 Genes GS174919: HP:0000767 Pectus excavatum
Expand Tier I Human 3 Genes GS172763: HP:0001686 Loss of voice
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 6 Genes GS173145: HP:0011281 Abnormality of urine catecholamine concentration
Expand Tier I Human GO 450 Genes GS197593: GO:0006091 generation of precursor metabolites and energy
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 28 Genes GS175889: HP:0100013 Neoplasm of the breast
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 25 Genes GS173554: HP:0005374 Cellular immunodeficiency
Expand Human 1417 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Human 1149 Genes GS219942: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 3 Genes GS176561: HP:0001011 Diaphoresis (with pheochromocytoma)
Expand Tier I Human GO 93 Genes GS193942: GO:0035383 thioester metabolic process
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 40 Genes GS172679: HP:0001028 Hemangioma
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 1 Genes GS174861: HP:0006723 Intestinal carcinoid
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 12 Genes GS171443: HP:0008777 Abnormality of the vocal cords
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 6 Genes GS174038: HP:0011976 Elevated urinary catecholamines
Expand Tier I Human 111 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Human GO 832 Genes GS194556: GO:0031975 envelope
Expand Human 1149 Genes GS219725: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 18 Genes GS175558: HP:0002516 Increased intracranial pressure
Expand Tier I Human 3 Genes GS176392: HP:0000740 Anxiety (with pheochromocytoma)
Expand Tier I Human 15 Genes GS177048: HP:0011371 Recurrent viral skin infections
Expand Tier I Human 16 Genes GS171687: HP:0003072 Hypercalcemia
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human CTD 476 Genes GS125040: Thioacetamide interacting genes (MeSH:D013853) in CTD
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 399 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Human 1661 Genes GS219987: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 3 Genes GS174401: HP:0001613 Hoarse voice (caused by tumor impingement)
Expand Tier I Human 10 Genes GS174848: HP:0200008 Intestinal polyposis
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 33 Genes GS174605: HP:0001609 Hoarse voice
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension
Expand Tier I Human 6 Genes GS174127: HP:0009903 Conjunctival nodules
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
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 117 Genes GS172364: HP:0003111 Abnormality of ion homeostasis
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human CTD 303 Genes GS123351: Omeprazole interacting genes (MeSH:D009853) in CTD
Expand Tier I Human GO 215 Genes GS199314: GO:0006732 coenzyme metabolic process
Expand Tier I Human 4 Genes GS172376: HP:0002864 Paraganglioma of head and neck
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 6 Genes GS174837: HP:0001095 Hypertensive retinopathy
Expand Tier I Human 4 Genes GS172446: HP:0003001 Glomus jugular tumor
Expand Tier I Human 138 Genes GS174289: HP:0002577 Abnormality of the stomach
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 60 Genes GS173119: HP:0002315 Headache
Expand Tier I Human 75 Genes GS175886: HP:0007378 Neoplasm of the gastrointestinal tract
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Human 968 Genes GS219975: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 144 Genes GS175128: HP:0011123 Inflammatory abnormality of the skin
Expand Tier I Human 39 Genes GS175738: HP:0011732 Abnormality of adrenal morphology
Expand Tier I Human 3 Genes GS175283: HP:0006748 Adrenal pheochromocytoma
Expand Tier I Human GO 58 Genes GS196470: GO:0042773 ATP synthesis coupled electron transport
Expand Tier I Human 128 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Human 1985 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 61 Genes GS174375: HP:0002027 Abdominal pain
Expand Human 1417 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 505 Genes GS198971: GO:0031966 mitochondrial membrane
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 709 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier I Human 11 Genes GS174608: HP:0001604 Vocal cord paresis
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 3 Genes GS173928: HP:0001675 Rhythm disturbances associated with pheochromocytoma
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human 3 Genes GS174610: HP:0001606 Vocal cord paralysis (caused by tumor impingement)
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 148 Genes GS203053: GO:0022900 electron transport chain
Expand Tier I Human GO 351 Genes GS198058: GO:0005743 mitochondrial inner membrane
Expand Tier I Human GO 13 Genes GS202368: GO:0048038 quinone binding
Expand Tier I Human 39 Genes GS173693: HP:0001649 Tachycardia
Expand Human 270 Genes GS222841: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_NEURONAL_SYSTEM
Expand Tier I Human 86 Genes GS172352: HP:0000137 Abnormality of the ovary
Expand Tier I Human 12 Genes GS175319: HP:0005266 Intestinal polyps
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human 177 Genes GS175431: HP:0011122 Abnormality of skin physiology
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 130 Genes GS199478: GO:0020037 heme binding
Expand Tier I Human GO 76 Genes GS204180: GO:0070469 respiratory chain
Expand Tier I Human 55 Genes GS174648: HP:0000957 Cafe-au-lait spot
Expand Human 982 Genes GS219939: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 3934 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 27 Genes GS175840: HP:0000739 Anxiety
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 5 Genes GS171920: HP:0002668 Paraganglioma
Expand Tier I Human 129 Genes GS174925: HP:0000769 Abnormality of the breast
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 70 Genes GS175064: HP:0000975 Hyperhidrosis
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 30 Genes GS175081: HP:0006753 Neoplasm of the stomach
Expand Tier I Human 66 Genes GS174437: HP:0005114 Abnormalities of the peripheral arteries
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 4 Genes GS207058: GO:0045283 fumarate reductase complex
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 13 Genes GS171993: HP:0100631 Neoplasm of the adrenal gland
Expand Human 1321 Genes GS219945: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 34 Genes GS174723: HP:0000771 Gynecomastia
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 9 Genes GS172307: HP:0100696 Bone cysts
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 4 Genes GS201364: GO:0045257 succinate dehydrogenase complex (ubiquinone)
Expand Human 1321 Genes GS219984: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human CTD 18 Genes GS123977: 2,6-dichloro-4-nitrophenol interacting genes (MeSH:C015802) in CTD
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier III Human 255 Genes GS213295: Meta-analysis of age-related gene expression profiles in the human brain
Expand Tier I Human 60 Genes GS176021: HP:0010927 Abnormality of divalent inorganic cation homeostasis
Expand Tier I Human 8 Genes GS171438: HP:0008776 Abnormality of the renal artery
Expand Tier I Human 4 Genes GS172026: HP:0000361 Pulsatile tinnitus (tympanic paraganglioma)
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD