Autosomal Domit Distal Hereditary Motor Neuronopathy 10
Disease ID: disease_node_18013
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| Dbxref | MIM:620080 |
|---|---|
| Subclassof | DOID_0111198 |
| Data Source | DOID |
| Doid Label | autosomal domit distal hereditary motor neuronopathy 10 |
| Doid Description | An autosomal domit distal hereditary motor neuronopathy that is characterized clinically by length-dependent motor neuropathy primarily affecting the lower limbs and that has_material_basis_in heterozygous mutation in the EMILIN1 gene on chromosome 2p23. |
| Disease Node Id | disease_node_18013 |
| Doid Id | DOID_0081399 |
| Label | Autosomal Domit Distal Hereditary Motor Neuronopathy 10 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Distal Hereditary Motor Neuronopathy(ID:disease_node_18002) (Disease)