Cadasil 2
Disease ID: disease_node_19912
Connections displayed (default: 10).
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| Dbxref | ICD10CM:F01.1, MIM:616779 |
|---|---|
| Subclassof | DOID_0050736, DOID_13945 |
| Data Source | DOID |
| Synonyms | autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2 |
| Doid Label | CADASIL 2 |
| Doid Description | A CADASIL characterized by stroke, transient ischemic attacks, cognitive impairment, dementia, balance impairment, gait disturbance, headaches, and/or seizures associated with early confluent or confluent diffuse white matter hyperintensities that has_material_basis_in heterozygous mutation in the HTRA1 gene on chromosome 10q26. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19912 |
| Doid Id | DOID_0111036 |
| Label | Cadasil 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cadasil(ID:disease_node_11298) (Disease)