All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01251 BHC chorea, hereditary, benign (BHC) 118700 AD 1 1 NKX2-1 - -
03000 CAHTP choreoathetosis, hypothyroidism, and neonatal respiratory distress (CAHTP) 610978 AD - - NKX2-1 - -
01583 NMTC1 cancer, thyroid, nonmedullary, type 1 (NMTC-1, papillary thyroid carcinoma) 188550 AD 1 - CCDC6, GOLGA5, NCOA4, NKX2-1, PCM1, PRKAR1A, TRIM24, TRIM33 - -
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