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DO Term : hereditary spastic paraplegia 18 [DOID:0110771] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the ERLIN2 gene on chromosome 8p11.

synonyms:
intellectual disability, motor dysfunction and joint contractures,
SPG18,
autosomal recessive spastic paraplegia type 18,
IDMDC,
GARD:4922,
611225,
ORDO:209951,
ICD10CM:G11.4,
autosomal recessive spastic paraplegia 18,
OMIM:611225

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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