All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00350 DFNA1 deafness, autosomal dominant, type 1 124900 AD 312 236 CEACAM16, DIAPH1, GRHL2 - -
06653 SCBMS Seizures, cortical blindness, microcephaly syndrome 616632 AR - - DIAPH1 - -
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