All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01298 ECTD10A dysplasia, ectodermal, type 10A, hypohidrotic/hair/nail, autosomal dominant (ECTD10A) 129490 AD 9 9 EDAR - -
01763 ECTD10B dysplasia, ectodermal, type 10B, hypohidrotic/hair/tooth, autosomal recessive (ECTD10B) 224900 AR 9 7 EDAR - -
03795 ECTD11A dysplasia, ectodermal, type 11A, hypohidrotic/hair/tooth, autosomal dominant (ECTD11A) 614940 AD 2 2 EDARADD - -
03796 ECTD11B dysplasia, ectodermal, type 11B, hypohidrotic/hair/tooth, autosomal recessive (ECTD11B) 614941 AR 0 0 EDARADD - -
03164 HRM1 hair morphology, type 1, thickness (HRM1) 612630 - 0 0 EDAR - -
02267 STHAGX1 agenesis, tooth, selective, X-linked, type 1 (STHAGX1) 313500 XLD 0 0 EDA - -
02233 XHED dysplasia, ectodermal, type 1, hypohidrotic, X-linked (XHED) 305100 - 199 194 EDA - -
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