Hereditary Sensory Neuropathy Type 1F
Disease ID: disease_node_19415
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| Dbxref | MIM:615632 |
|---|---|
| Subclassof | DOID_0050736, DOID_0070162 |
| Data Source | DOID |
| Synonyms | HSN1F, hereditary sensory neuropathy type IF |
| Doid Label | hereditary sensory neuropathy type 1F |
| Doid Description | A hereditary sensory and autonomic neuropathy type 1 characterized by distal sensory impairment becomes apparent during the second or third decade of life, resulting in painless ulceration of the feet with poor healing, which can progress to osteomyelitis, bone destruction, and amputation that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_19415 |
| Doid Id | DOID_0070154 |
| Label | Hereditary Sensory Neuropathy Type 1F |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)