FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	Charcot-Marie-Tooth disease type 1	ID (Ontology)	DOID:0050538 (Human Disease)
Definition	A Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons.
Also Known As	"hereditary motor and sensory neuropathy type 1"
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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Spanning Tree (Parents/Children)

  neuromuscular disease
   |__Charcot-Marie-Tooth disease
       |__Charcot-Marie-Tooth disease type 1  12 rec.
           |__Charcot-Marie-Tooth disease type 1A
           |__Charcot-Marie-Tooth disease type 1B
           |__Charcot-Marie-Tooth disease type 1C 10 rec.
           |__Charcot-Marie-Tooth disease type 1D 1 rec.
           |__Charcot-Marie-Tooth disease type 1E
           |__Charcot-Marie-Tooth disease type 1F
           |__Charcot-Marie-Tooth disease type 1G 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
	"hereditary motor and sensory neuropathy type 1" EXACT
Secondary IDs

External Crossreferences & Linkouts
	GARD:12433