WormBase Tree Display for DO_term: DOID:0110792
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DOID:0110792 | Name | hereditary spastic paraplegia 4 | |||
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Status | Valid | ||||
Definition | A hereditary spastic paraplegia that is characterized by slowly progressive muscle weakness and spasticity and has_material_basis_in mutation in the SPAST gene on chromosome 2p22. | ||||
Synonym | Exact | SPG4 | |||
autosomal dominant spastic paraplegia 4 | |||||
autosomal dominant spastic paraplegia type 4 | |||||
Parent | Is_a | DOID:2476 | |||
DOID:0050736 | |||||
DB_info | Database | OMIM | disease | 182601 | |
Attribute_of | Gene_by_orthology | WBGene00016045 |