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DO Term : Charcot-Marie-Tooth disease type 4 [DOID:0050541] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance.

synonyms:
GARD:12440,
ORDO:64749,
DOID:0050582,
hereditary motor and sensory neuropathy

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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