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DO Term : Charcot-Marie-Tooth disease X-linked recessive 4 [DOID:0110212] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Charcot-Marie-Tooth disease X-linked that has_material_basis_in mutation in the AIFM1 gene on chromosome Xq26.

synonyms:
axonal motor sensory neuropathy with deafness and mental retardation,
CMTX4,
ORDO:101078,
OMIM:310490,
Cowchock syndrome,
ICD10CM:G60.0,
NADMR,
NAMSD,
X-linked Charcot-Marie-Tooth disease type 4,
CMT4X,
310490,
Charcot-Marie-Tooth disease with deafness and mental retardation

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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