Disease #03092 (EDAID2 (dysplasia, ectodermal, and immunodeficiency, type 2), OMIM:612132)

Official abbreviation EDAID2
Name dysplasia, ectodermal, and immunodeficiency, type 2
OMIM ID 612132
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NFKBIA
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2026-02-13 08:57:52 +01:00 (CET)

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