ZFIN Human Disease: autosomal dominant distal hereditary motor neuronopathy 4

OBO ID: DOID:0111209

Term Name:	autosomal dominant distal hereditary motor neuronopathy 4		Search Ontology:
Synonyms:	DHMN2C distal hereditary motor neuronopathy type 2C distal hereditary motor neuropathy type IIC HMN IIC HMN2C
Definition:	A distal hereditary motor neuropathy that has_material_basis_in heterozygous mutation in the HSPB3 gene on 5q11.2. https://www.ncbi.nlm.nih.gov/pubmed/20142617
References:	OMIM:613376
Ontology:	Human Disease ( DOID:0111209 )

Relationships

is a type of:	autosomal dominant distal hereditary motor neuronopathy autosomal dominant distal hereditary motor neuronopathy Show first 5 Terms

OTHER autosomal dominant distal hereditary motor neuronopathy 4 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HSPB3	hspb3	?Neuronopathy, distal hereditary motor, autosomal dominant 4	613376

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None