nemaline myopathy 10

Summary

nemaline myopathy 10 is a rare disease^[1].

Key Facts

• nemaline myopathy 10's instance of is recorded as rare disease^[2].
• nemaline myopathy 10's instance of is recorded as class of disease^[3].
• nemaline myopathy 10's subclass of is recorded as nemaline myopathy^[4].
• nemaline myopathy 10's subclass of is recorded as Typical nemaline myopathy^[5].
• nemaline myopathy 10's subclass of is recorded as severe congenital nemaline myopathy^[6].
• nemaline myopathy 10's subclass of is recorded as genetic disease^[7].
• nemaline myopathy 10's subclass of is recorded as autosomal recessive disease^[8].
• nemaline myopathy 10's OMIM ID is recorded as 616165^[9].
• nemaline myopathy 10's OMIM ID is recorded as 616165^[10].
• nemaline myopathy 10's Disease Ontology ID is recorded as DOID:0110931^[11].
• nemaline myopathy 10's genetic association is recorded as LMOD3^[12].
• nemaline myopathy 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110931^[13].
• nemaline myopathy 10's exact match is recorded as http://identifiers.org/doid/DOID:0110931^[14].
• nemaline myopathy 10's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_607^[15].
• nemaline myopathy 10's UMLS CUI is recorded as C4015360^[16].
• nemaline myopathy 10's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• nemaline myopathy 10's Mondo ID is recorded as MONDO_0014513^[18].
• nemaline myopathy 10's UniProt disease ID is recorded as DI-04292^[19].