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Metadata
ID DOID:0110768
Name hereditary spastic paraplegia 15
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1.
https://www.ncbi.nlm.nih.gov/pubmed/18394578
Xrefs

GARD:9581

ICD10CM:G11.4

OMIM:270700

ORDO:100996

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 15 [EXACT]

autosomal recessive spastic paraplegia type 15 [EXACT]

hereditary spastic paraparesis type 15 [EXACT]

Kjellin syndrome [EXACT]

spastic paraplegia and retinal degeneration [EXACT]

spastic paraplegia-retinal degeneration syndrome [EXACT]

SPG15 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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