FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Charcot-Marie-Tooth disease type 4 ID (Ontology) DOID:0050541 (Human Disease)
Definition A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance.
Also Known As "hereditary motor and sensory neuropathy"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship:
  neuromuscular disease
   |__Charcot-Marie-Tooth disease
       |__Charcot-Marie-Tooth disease type 4  39 rec.
           |__autosomal recessive axonal Charcot-Marie-Tooth disease with vocal cord paresis 1 rec.
           |__Charcot-Marie-Tooth disease type 4A 2 rec.
           |__Charcot-Marie-Tooth disease type 4B1 24 rec.
           |__Charcot-Marie-Tooth disease type 4B2 1 rec.
           |__Charcot-Marie-Tooth disease type 4B3 1 rec.
           |__Charcot-Marie-Tooth disease type 4C
           |__Charcot-Marie-Tooth disease type 4D 2 rec.
           |__Charcot-Marie-Tooth disease type 4E 1 rec.
           |__Charcot-Marie-Tooth disease type 4F
           |__Charcot-Marie-Tooth disease type 4G 1 rec.
           |__Charcot-Marie-Tooth disease type 4H 1 rec.
           |__Charcot-Marie-Tooth disease type 4J 6 rec.
           |__Charcot-Marie-Tooth disease type 4K 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a Charcot-Marie-Tooth disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "hereditary motor and sensory neuropathy" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:12440
ORDO:64749