Hereditary Spastic Paraplegia 87
Disease ID: disease_node_16677
Connections displayed (default: 10).
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| Dbxref | MIM:619966 |
|---|---|
| Subclassof | DOID_2476, DOID_0050737 |
| Data Source | DOID |
| Synonyms | SPG87, autosomal recessive spastic paraplegia 87 |
| Doid Label | hereditary spastic paraplegia 87 |
| Doid Description | A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM63C gene on chromosome 14q24.3. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16677 |
| Doid Id | DOID_0070456 |
| Label | Hereditary Spastic Paraplegia 87 |
- 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)