ZFIN Human Disease: Charcot-Marie-Tooth disease type 1F

OBO ID: DOID:0110149

Term Name:	Charcot-Marie-Tooth disease type 1F		Search Ontology:
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 Charcot-Marie-Tooth disease type 1F PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NEFL	nefla neflb	Charcot-Marie-Tooth disease, type 1F	607734

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None