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
02238 HTX1 heterotaxy, visceral, X-linked, type 1, (HTX-1, situs inversus/situs ambiguus) 306955 XLR 36 36 ZIC3 - -
02270 VACTERLX VACTERL association with hydrocephaly, X-linked (VACTERLX) 314390 XLR 1 1 FANCB, ZIC3 - -
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