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Human Disease

Charcot-Marie-Tooth disease type 1F

Term ID

DOID:0110149

Synonyms

Charcot-Marie-Tooth neuropathy type 1F
CMT1F

Definition

A Charcot-Marie-Tooth disease type 1 that has_material_basis_in mutation in the NEFL gene. https://www.ncbi.nlm.nih.gov/pubmed/12566280

References

ICD10CM:G60.0
OMIM:607734
ORDO:101085

Ontology

Human Disease ( DOID:0110149 )

Relationships

is a type of: autosomal dominant disease autosomal recessive disease Charcot-Marie-Tooth disease type 1

autosomal dominant disease autosomal recessive disease Charcot-Marie-Tooth disease type 1 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations