Autosomal Recessive Distal Hereditary Motor Neuronopathy 9
Disease ID: disease_node_18018
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| Dbxref | MIM:620402 |
|---|---|
| Subclassof | DOID_0111197 |
| Data Source | DOID |
| Doid Label | autosomal recessive distal hereditary motor neuronopathy 9 |
| Doid Description | An autosomal recessive distal hereditary motor neuronopathy characterized by juvenile onset of distal muscle weakness and atrophy, resulting in gait difficulties and that has_material_basis_in homozygous or compound heterozygous mutation in the COQ7 gene on chromosome 16p12. |
| Existence Starts During | HP_0003621 |
| Disease Node Id | disease_node_18018 |
| Doid Id | DOID_0081428 |
| Label | Autosomal Recessive Distal Hereditary Motor Neuronopathy 9 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Distal Hereditary Motor Neuronopathy(ID:disease_node_18014) (Disease)