Hereditary Sensory Neuropathy Type 1E
Disease ID: disease_node_19422
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| Dbxref | GARD:11927, ICD10CM:G60.8, MIM:614116, ORDO:456318 |
|---|---|
| Subclassof | DOID_0050736, DOID_0050548 |
| Data Source | DOID |
| Synonyms | HSN1E, hereditary sensory neuropathy type IE |
| Doid Label | hereditary sensory neuropathy type 1E |
| Doid Description | A hereditary sensory neuropathy characterized by adult onset of progressive peripheral sensory loss, progressive hearing impairment, and early-onset dementia that has_material_basis_in heterozygous mutation in the DNMT1 gene on chromosome 19p13. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19422 |
| Doid Id | DOID_0070158 |
| Label | Hereditary Sensory Neuropathy Type 1E |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)