Related MeSH Hierarchy (6)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Ectodermal Dysplasia » Ectodermal Dysplasia 1, Anhidrotic
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Ectodermal Dysplasia » Ectodermal Dysplasia 1, Anhidrotic
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Genetic Diseases, X-Linked » Ectodermal Dysplasia 1, Anhidrotic
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Ectodermal Dysplasia » Ectodermal Dysplasia 1, Anhidrotic
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Ectodermal Dysplasia » Ectodermal Dysplasia 1, Anhidrotic
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Ectodermal Dysplasia » Ectodermal Dysplasia 1, Anhidrotic
Description
An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN. MeSH
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Phase 2 Indicated Drugs (1)
Phase 1 Indicated Drugs (1)
Organization Involved with Phase 2 Indications (1)
Organization Involved with Phase 1 Indications (1)
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