ZFIN Human Disease: Charcot-Marie-Tooth disease dominant intermediate F

OBO ID: DOID:0110206

Term Name:	Charcot-Marie-Tooth disease dominant intermediate F		Search Ontology:
Synonyms:	autosomal dominant intermediate Charcot-Marie-Tooth disease type F CMTDIF
Definition:	A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in heterozygous mutation in the GNB4 gene on chromosome 3q28. https://www.ncbi.nlm.nih.gov/pubmed/23434117
References:	ICD10CM:G60.0 OMIM:615185 ORDO:352670
Ontology:	Human Disease ( DOID:0110206 )

Relationships

is a type of:	autosomal dominant disease Charcot-Marie-Tooth disease intermediate type autosomal dominant disease Charcot-Marie-Tooth disease intermediate type Show first 5 Terms

OTHER Charcot-Marie-Tooth disease dominant intermediate F PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GNB4	gnb4b gnb4a	Charcot-Marie-Tooth disease, dominant intermediate F	615185

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None