Hereditary Spastic Paraplegia 89
Disease ID: disease_node_16675
Connections displayed (default: 10).
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| Dbxref | MIM:620379 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG89, autosomal recessive spastic paraplegia 89 |
| Doid Label | hereditary spastic paraplegia 89 |
| Doid Description | A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16675 |
| Doid Id | DOID_0070458 |
| Label | Hereditary Spastic Paraplegia 89 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease)