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
00665 BNAR Bifid nose with/without anorectal and renal anomalies 608980 - 2 0 FREM1 - -
00666 MOTA Manitoba oculotrichoanal syndrome (MOTA) 248450 AR 2 0 FREM1 - -
00667 TRIGNO2 trigonocephaly, type 2 (TRIGNO-2) 614485 AD 2 0 FREM1 - -
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