Ectodermal Dysplasia 15
Disease ID: disease_node_18086
Connections displayed (default: 10).
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| Dbxref | MIM:618535 |
|---|---|
| Subclassof | DOID_0050737, DOID_2121 |
| Data Source | DOID |
| Synonyms | ECTD15, ectodermal dysplasia 15, hypohidrotic/hair type |
| Doid Label | ectodermal dysplasia 15 |
| Doid Description | An ectodermal dysplasia characterized by onset in early childhood of hypotrichosis and absence of sweating except with extreme exercise that has_material_basis_in homozygous or compound heterozygous mutation in the CST6 gene on chromosome 11q13.1. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_18086 |
| Doid Id | DOID_0111651 |
| Label | Ectodermal Dysplasia 15 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)