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DO Term : hereditary spastic paraplegia 89 [DOID:0070458] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13.

synonyms:
OMIM:620379,
SPG89,
autosomal recessive spastic paraplegia 89,
620379

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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