cap myopathy

Summary

cap myopathy is a class of disease^[1].

Key Facts

• cap myopathy's instance of is recorded as class of disease^[2].
• cap myopathy's subclass of is recorded as congenital myopathy^[3].
• cap myopathy's MeSH descriptor ID is recorded as C579969^[4].
• cap myopathy's KEGG ID is recorded as H00702^[5].
• cap myopathy's Orphanet ID is recorded as 171881^[6].
• cap myopathy's genetic association is recorded as TPM3^[7].
• cap myopathy's genetic association is recorded as TPM2^[8].
• cap myopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_171881^[9].
• cap myopathy's UMLS CUI is recorded as C3710589^[10].
• cap myopathy's ICD-10-CM is recorded as G71.2^[11].
• cap myopathy's GARD rare disease ID is recorded as 11915^[12].
• cap myopathy's Mondo ID is recorded as MONDO_0015753^[13].
• cap myopathy's Genetics Home Reference Conditions ID is recorded as cap-myopathy^[14].