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DO Term : hereditary spastic paraplegia 51 [DOID:0110803] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4E1 gene on chromosome 15q21.

synonyms:
613744,
SPG51,
OMIM:613744,
spastic quadriplegic cerebral palsy 4,
ORDO:280763,
CPSQ4,
autosomal dominant spastic paraplegia 51,
GARD:10999

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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