ZFIN Human Disease: Charcot-Marie-Tooth disease type 4G

OBO ID: DOID:0110196

Term Name:	Charcot-Marie-Tooth disease type 4G		Search Ontology:
Synonyms:	autosomal recessive Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth neuropathy type 4G CMT4G HMSNR
Definition:	A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22. https://www.ncbi.nlm.nih.gov/pubmed/19536174
References:	ICD10CM:G60.0 OMIM:605285 ORDO:99953
Ontology:	Human Disease ( DOID:0110196 )

Relationships

is a type of:	autosomal recessive disease Charcot-Marie-Tooth disease type 4 autosomal recessive disease Charcot-Marie-Tooth disease type 4 Show first 5 Terms

OTHER Charcot-Marie-Tooth disease type 4G PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HK1	hk1	Neuropathy, hereditary motor and sensory, Russe type	605285

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None