ZFIN Human Disease: autosomal dominant distal hereditary motor neuronopathy 14

OBO ID: DOID:0111202

Term Name:	autosomal dominant distal hereditary motor neuronopathy 14		Search Ontology:
Synonyms:	DHMN7B distal hereditary motor neuronopathy type 7B distal hereditary motor neuropathy type VIIB distal spinal muscular atrophy with vocal cord paralysis type 7B Harper-Young myopathy HMN VIIB HMN7B
Definition:	An autosomal dominant distal hereditary motor neuronopathy that has_material_basis_in heterozygous mutation in the DCTN1 gene on 2p13.1. https://www.ncbi.nlm.nih.gov/pubmed/12627231
References:	OMIM:607641
Ontology:	Human Disease ( DOID:0111202 )

Relationships

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

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DCTN1	dctn1b dctn1a	Neuronopathy, distal hereditary motor, autosomal dominant 14	607641

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None