Hereditary Spastic Paraplegia 90B
Disease ID: disease_node_16673
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| Dbxref | MIM:620417 |
|---|---|
| Subclassof | DOID_0050736, DOID_2476 |
| Data Source | DOID |
| Synonyms | SPG90B, autosomal recessive spastic paraplegia 90B |
| Doid Label | hereditary spastic paraplegia 90B |
| Doid Description | A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in homozygous mutation in the SPTSSA gene on chromosome 14q13.1. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_16673 |
| Doid Id | DOID_0070460 |
| Label | Hereditary Spastic Paraplegia 90B |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Spastic Paraplegia, Hereditary(ID:disease_node_8225) (Disease)