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DO Term : Charcot-Marie-Tooth disease type 6 [DOID:0080068] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A Charcot-Marie-Tooth disease that is characterized by early-onset optic atrophy resulting in progressive visual loss and peripheral axonal sensorimotor neuropathy with highly variable age at onset and severity.
  • synonyms:
  • OMIM:601152,
  • OMIM:616505,
  • 601152,
  • hereditary motor and sensory neuropathy type 6,
  • 616505
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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