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DOID:0110934 - nemaline myopathy 7
Disease Ontology Definition:A nemaline myopathy characterized by very early onset of hypotonia and delayed motor development that has_material_basis_in homozygous mutation in the CFL2 gene on chromosome 14q13.
Synonyms: NEM7, nemaline myopathy 7, autosomal recessive
Xenbase Genes : cfl2
MONDO:0012538 - nemaline myopathy 7 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee