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DO Term : hereditary spastic paraplegia 52 [DOID:0110804] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4S1 gene on chromosome 14q12.

synonyms:
autosomal recessive spastic paraplegia 52,
ORDO:280763,
614067,
OMIM:614067,
CPSQ6,
SPG52,
spastic quadriplegic cerebral palsy 6

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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