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
00367 ECTD3 dysplasia, ectodermal, type 3 (ECTD-3, Witkop syndrome, tooth and nail syndrome) 189500 AD 1 1 MSX1 - -
00366 OFC5 orofacial cleft, type 5 (OFC-5, cleft lip with/without cleft palate) 608874 - 24 24 MSX1 - -
00368 STHAG1 agenesis, tooth, selective, with/without orofacial cleft, type 1 (STHAG-1) 106600 AD 19 17 MSX1 - -
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