Hereditary Spastic Paraplegia 32
Disease ID: disease_node_16626
Connections displayed (default: 10).
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| Dbxref | GARD:12749, ICD10CM:G11.4, MIM:611252, ORDO:171622 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG32, autosomal recessive spastic paraplegia 32, autosomal recessive spastic paraplegia type 32 |
| Doid Label | hereditary spastic paraplegia 32 |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16626 |
| Doid Id | DOID_0110783 |
| Label | Hereditary Spastic Paraplegia 32 |
- 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)