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DO Term : hereditary spastic paraplegia 44 [DOID:0110796] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the GJC2 gene on chromosome 1q42.

synonyms:
ORDO:320401,
613206,
OMIM:613206,
autosomal recessive spastic paraplegia 44,
ICD10CM:G11.4,
SPG44

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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