All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01962 - myxoma, intracardiac 255960 AD - - PRKAR1A - -
01160 ACRDYS1 acrodysostosis, with/without hormone resistance 101800 AD 39 33 PRKAR1A - flat anterior facies, mid-face hypoplasia, hypertelorism, small nose, depressed nasal bridge, short columella, long philtrum, prominent chin; no seizure (-HP:0001250); no hypotonia (-HP:0001252); short stature (HP:0004322); obesity (HP:0001513); digital abnormalities (HP_0011297); severe brachydactyly, skeletal dysplasia, multiple hormone resistance
01459 CNC1 Carney complex, type 1 (CNC-1) 160980 AD 1 1 PRKAR1A - -
01583 NMTC1 cancer, thyroid, nonmedullary, type 1 (NMTC-1, papillary thyroid carcinoma) 188550 AD 1 - CCDC6, GOLGA5, NCOA4, NKX2-1, PCM1, PRKAR1A, TRIM24, TRIM33 - -
02950 PPNAD1 adrenocortical disease, nodular, pigmented, primary, type 1 (PPNAD-1) 610489 AD - - PRKAR1A - -
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