All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01365 HSCR1 Hirschsprung disease, type 1 (HSCR1) 142623 AD 6 1 RET - -
01504 MEN2A neoplasia, endocrine, multiple, type II1 (MEN-2A) 171400 AD - - RET - -
01465 MEN2B neoplasia, endocrine, multiple, type IIb (MEN-2B) 162300 AD - - RET - -
01428 MTC carcinoma, thyroid, medullary, familial (MTC) 155240 AD 22 1 RET - -
00151 NIDDM diabetes mellitus, type II (NIDDM) 125853 AD 8 7 ABCC8, AKT2, CDKAL1, ENPP1, GCGR, GCK, GPD2, HMGA1, HNF1A, HNF1B, HNF4A, IGF2BP2, IRS1, IRS2, KCNJ11, LIPC, MAPK8IP1, MTNR1B, NEUROD1, PAX4, 8 more - -
01503 pheochromocytoma pheochromocytoma (susceptibility to) 171300 AD 146 142 MAX, RET, TMEM127, VHL cerebral cortex -
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