Search Ontology:
Human Disease
hereditary spastic paraplegia 7
- Term ID
- DOID:0110816
- Synonyms
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- autosomal recessive spastic paraplegia 7
- spastic paraplegia type 7
- SPG7
- 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. https://www.ncbi.nlm.nih.gov/pubmed/9635427
- References
-
- ICD10CM:G11.4
- MIM:607259
- ORDO:99013
- Ontology
- Human Disease ( DOID:0110816 )
- is a type of
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