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Ectodermal Dysplasia 1, Anhidrotic

Disease ID: disease_node_11687

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DbxrefMESH:D053358, MIM:305100, NCI:C84562, ORDO:181, SNOMEDCT_US_2023_03_01:239007005, UMLS_CUI:C0162359
SubclassofDOID_0080012, DOID_14793
Data SourceDOID, MESH
SynonymsCST syndrome, Christ-Siemens-Touraine syndrome, ED1, HED1, X-linked anhidrotic ectodermal dysplasia, XHED, XLHED, ectodermal dysplasia 1, anhidrotic, ectodermal dysplasia 1, hypohidrotic, X-linked, ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked, hypohidrotic ectodermal dysplasia, X-Linked
Mesh IdD053358
Mesh LabelEctodermal Dysplasia 1, Anhidrotic
Mesh SubclassofD040181, D004476
Doid Labelectodermal dysplasia 1
Doid DescriptionA hypohidrotic ectodermal dysplasia that has_material_basis_in X-linked recessive mutation in EDA on chromosome Xq13.1.
Has Material Basis InGENO_0000149
Disease Node Iddisease_node_11687
Doid IdDOID_0111664
LabelEctodermal Dysplasia 1, Anhidrotic