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Disease Ontology Browser
hereditary spastic paraplegia 7 (DOID:0110816)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 7; spastic paraplegia type 7; SPG7
Alt IDs: OMIM:607259, ICD10CM:G11.4, ORDO:99013
Definition: A hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has_material_basis_in mutation in the SPG7 gene on chromosome 16q24.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.20
The Jackson Laboratory