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DO Term : hereditary spastic paraplegia 15 [DOID:0110768] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the ZFYVE26 gene on chromosome 14q24.1.

synonyms:
spastic paraplegia and retinal degeneration,
Kjellin syndrome,
autosomal recessive spastic paraplegia 15,
spastic paraplegia-retinal degeneration syndrome,
autosomal recessive spastic paraplegia type 15,
270700,
hereditary spastic paraparesis type 15,
OMIM:270700,
ORDO:100996,
ICD10CM:G11.4,
GARD:9581,
SPG15

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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