ZFIN Human Disease: nemaline myopathy 2

OBO ID: DOID:0110928

OBO ID: DOID:0110928

Term Name:	nemaline myopathy 2	Search Ontology:
Synonyms:	congenital myopathy 2 NEM2 nemaline myopathy 2, autosomal recessive
Definition:	A nemaline myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23. (2)
References:	MESH:C538349 OMIM:256030
Ontology:	Human Disease ( DOID:0110928 )

Relationships

is a type of:	autosomal recessive disease nemaline myopathy autosomal recessive disease nemaline myopathy Show first 5 Terms

OTHER nemaline myopathy 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
NEB	neb	Nemaline myopathy 2, autosomal recessive	256030

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None