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DO Term : hereditary spastic paraplegia 35 [DOID:0110786] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1.

synonyms:
OMIM:612319,
leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia,
612319,
ICD10CM:G11.4,
autosomal recessive spastic paraplegia type 35,
SPG35,
fatty acid hydroxylase-associated neurodegeneration,
autosomal recessive spastic paraplegia 35,
ORDO:171629,
FAHN

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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