FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	Charcot-Marie-Tooth disease type X	ID (Ontology)	DOID:0050542 (Human Disease)
Definition	A Charcot-Marie-Tooth disease that has_material_basis_in X-linked inheritance of a point mutation in the connexin-32 gene.
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Spanning Tree (Parents/Children)

  neuromuscular disease
   |__Charcot-Marie-Tooth disease
       |__Charcot-Marie-Tooth disease type X  3 rec.
           |__Charcot-Marie-Tooth disease X-linked dominant 1
           |__Charcot-Marie-Tooth disease X-linked dominant 6 1 rec.
           |__Charcot-Marie-Tooth disease X-linked recessive 2
           |__Charcot-Marie-Tooth disease X-linked recessive 3
           |__Charcot-Marie-Tooth disease X-linked recessive 4 1 rec.
           |__Charcot-Marie-Tooth disease X-linked recessive 5 1 rec.

Spanning Tree View Settings
Parents/Children View Depth	Show hierarchy levels: for parents, for children
Relationships
Is a	Charcot-Marie-Tooth disease
Part of
Synonyms & Secondary IDs
Synonyms

Secondary IDs

External Crossreferences & Linkouts
	ORDO:64747