ZFIN Human Disease: autosomal recessive centronuclear myopathy

OBO ID: DOID:0111216

Term Name:	autosomal recessive centronuclear myopathy		Search Ontology:
Synonyms:	AR-CNM
Definition:	A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance. https://www.ncbi.nlm.nih.gov/pubmed/30103348
References:	GARD:12718 ORDO:169186
Ontology:	Human Disease ( DOID:0111216 )

Relationships

is a type of:	autosomal recessive disease centronuclear myopathy autosomal recessive disease centronuclear myopathy Show first 5 Terms
has subtype:	centronuclear myopathy 2 centronuclear myopathy 5 centronuclear myopathy 6 with fiber-type disproportion centronuclear myopathy 2 centronuclear myopathy 5 centronuclear myopathy 6 with fiber-type disproportion Show first 5 Terms

OTHER autosomal recessive centronuclear myopathy PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS

Fish	Conditions	Citations
spega^{hsc191/hsc191}; spegb^{hsc192/hsc192} (AB)	standard conditions	Espinosa et al., 2022

PHENOTYPE No data available

CITATIONS (1)