Ectodermal Dysplasia 1, Anhidrotic
Disease ID: disease_node_11687
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| Dbxref | MESH:D053358, MIM:305100, NCI:C84562, ORDO:181, SNOMEDCT_US_2023_03_01:239007005, UMLS_CUI:C0162359 |
|---|---|
| Subclassof | DOID_0080012, DOID_14793 |
| Data Source | DOID, MESH |
| Synonyms | CST 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 Id | D053358 |
| Mesh Label | Ectodermal Dysplasia 1, Anhidrotic |
| Mesh Subclassof | D040181, D004476 |
| Doid Label | ectodermal dysplasia 1 |
| Doid Description | A hypohidrotic ectodermal dysplasia that has_material_basis_in X-linked recessive mutation in EDA on chromosome Xq13.1. |
| Has Material Basis In | GENO_0000149 |
| Disease Node Id | disease_node_11687 |
| Doid Id | DOID_0111664 |
| Label | Ectodermal Dysplasia 1, Anhidrotic |
- Outgoing r'ship
SUBCLASS_OFto/from X-Linked Recessive Disease(ID:disease_node_13254) (Disease)