nemaline myopathy 1

Summary

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

Key Facts

• nemaline myopathy 1's instance of is recorded as rare disease^[2].
• nemaline myopathy 1's instance of is recorded as class of disease^[3].
• nemaline myopathy 1's subclass of is recorded as nemaline myopathy^[4].
• nemaline myopathy 1's subclass of is recorded as genetic disease^[5].
• nemaline myopathy 1's MeSH descriptor ID is recorded as C538348^[6].
• nemaline myopathy 1's OMIM ID is recorded as 609284^[7].
• nemaline myopathy 1's OMIM ID is recorded as 609284^[8].
• nemaline myopathy 1's Disease Ontology ID is recorded as DOID:0110926^[9].
• nemaline myopathy 1's genetic association is recorded as TPM3^[10].
• nemaline myopathy 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110926^[11].
• nemaline myopathy 1's exact match is recorded as http://identifiers.org/doid/DOID:0110926^[12].
• nemaline myopathy 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_171881^[13].
• nemaline myopathy 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_607^[14].
• nemaline myopathy 1's UMLS CUI is recorded as C1836448^[15].
• nemaline myopathy 1's UMLS CUI is recorded as C3714994^[16].
• nemaline myopathy 1's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].
• nemaline myopathy 1's Mondo ID is recorded as MONDO_0012239^[18].