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
05383 HSAN neuropathy, sensory and autonomic, hereditary (HSAN) - - 22 22 IKBKAP - -
01758 HSAN3 neuropathy, sensory and autonomic, hereditary, type III (HSAN-3, dysautonomia) 223900 AR - - IKBKAP - -
01429 MDB medulloblastoma (MDB) 155255 AD;AR;SMu 33 31 BRCA2, CTNNB1, IKBKAP, PTCH2, SUFU - -
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