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Disease Ontology Browser
hereditary spastic paraplegia 15 (DOID:0110768)
Alliance: disease page
Synonyms: autosomal recessive spastic paraplegia 15; autosomal recessive spastic paraplegia type 15; hereditary spastic paraparesis type 15; Kjellin syndrome; spastic paraplegia and retinal degeneration; spastic paraplegia-retinal degeneration syndrome; SPG15
Alt IDs: OMIM:270700, ICD10CM:G11.4, ORDO:100996
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1.

Disease References using Mouse Models (1)

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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