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nemaline myopathy 10

Go to external page http://purl.obolibrary.org/obo/MONDO_0014513

Any nemaline myopathy in which the cause of the disease is a mutation in the LMOD3 gene. [ MONDO:patterns/disease_series_by_gene ]

Synonyms: nemaline myopathy 10 nemaline myopathy caused by mutation in LMOD3 LMOD3 nemaline myopathy NEM10 nemaline myopathy type 10

This is just here as a test because I lose it

Term information

database cross reference
Subsets

gard_rare, rare, nord_rare, clingen

exactMatch

http://linkedlifedata.com/resource/umls/id/C4015360

https://omim.org/entry/616165

http://purl.obolibrary.org/obo/DOID_0110931

id

MONDO:0014513

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0014513