Epidermolytic Hyperkeratosis 2
Disease ID: disease_node_19967
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| Dbxref | MIM:620150 |
|---|---|
| Subclassof | DOID_4603 |
| Data Source | DOID |
| Doid Label | epidermolytic hyperkeratosis 2 |
| Doid Description | An epidermolytic hyperkeratosis that is characterized by generalized erythema, erosions, scaling, and easily breaking blisters that become less frequent later in life, while hyperkeratosis increases and that has_material_basis_in heterozygous or homozygous mutation in the keratin-10 gene (KRT10) on chromosome 17q21. |
| Disease Node Id | disease_node_19967 |
| Doid Id | DOID_0081359 |
| Label | Epidermolytic Hyperkeratosis 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Hyperkeratosis, Epidermolytic(ID:disease_node_9179) (Disease)