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DO Term : Charcot-Marie-Tooth disease type 4B3 [DOID:0110194] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous or compound heterozygous mutation in the SBF1 gene on chromosome 22q.
  • synonyms:
  • 615284,
  • CMT4B3,
  • ORDO:363981,
  • ICD10CM:G60.0,
  • OMIM:615284
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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





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