Hereditary Spastic Paraplegia 9B
Disease ID: disease_node_16646
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| Dbxref | ICD10CM:G11.4, MIM:616586, ORDO:447760 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG9B, autosomal recessive complex spastic paraplegia type 9B, autosomal recessive spastic paraplegia 9B |
| Doid Label | hereditary spastic paraplegia 9B |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16646 |
| Doid Id | DOID_0110825 |
| Label | Hereditary Spastic Paraplegia 9B |
- 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)