Hereditary Spastic Paraplegia 72A
Disease ID: disease_node_16654
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G11.4, MIM:615625, ORDO:401849 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG72, autosomal spastic paraplegia type 72 |
| Doid Label | hereditary spastic paraplegia 72A |
| Doid Description | A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2. |
| Has Material Basis In | GENO_0000147, GENO_0000148 |
| Disease Node Id | disease_node_16654 |
| Doid Id | DOID_0110817 |
| Label | Hereditary Spastic Paraplegia 72A |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - 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)