King-Denborough syndrome

Summary

King-Denborough syndrome is a class of disease^[1].

Key Facts

• King-Denborough syndrome's instance of is recorded as class of disease^[2].
• King-Denborough syndrome's subclass of is recorded as congenital myopathy^[3].
• King-Denborough syndrome's MeSH descriptor ID is recorded as C536883^[4].
• King-Denborough syndrome's MeSH descriptor ID is recorded as C537504^[5].
• King-Denborough syndrome's Orphanet ID is recorded as 99741^[6].
• King-Denborough syndrome's genetic association is recorded as RYR1^[7].
• King-Denborough syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_99741^[8].
• King-Denborough syndrome's UMLS CUI is recorded as C2931510^[9].
• King-Denborough syndrome's UMLS CUI is recorded as C1840365^[10].
• King-Denborough syndrome's ICD-10-CM is recorded as G71.2^[11].
• King-Denborough syndrome's GARD rare disease ID is recorded as 8561^[12].
• King-Denborough syndrome's Mondo ID is recorded as MONDO_0020485^[13].