3MC syndrome

Summary

3MC syndrome is a rare disease^[1].

Key Facts

• 3MC syndrome's instance of is recorded as rare disease^[2].
• 3MC syndrome's instance of is recorded as class of disease^[3].
• 3MC syndrome's subclass of is recorded as syndrome^[4].
• 3MC syndrome's subclass of is recorded as autosomal recessive disease^[5].
• 3MC syndrome's KEGG ID is recorded as H01887^[6].
• 3MC syndrome's Disease Ontology ID is recorded as DOID:0060225^[7].
• 3MC syndrome's symptoms and signs is recorded as ptosis^[8].
• 3MC syndrome's Orphanet ID is recorded as 293843^[9].
• 3MC syndrome's health specialty is recorded as medical genetics^[10].
• 3MC syndrome's genetic association is recorded as COLEC11^[11].
• 3MC syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060225^[12].
• 3MC syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060225^[13].
• 3MC syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_293843^[14].
• 3MC syndrome's UMLS CUI is recorded as C0796279^[15].
• 3MC syndrome's UMLS CUI is recorded as C4303860^[16].
• 3MC syndrome's ICD-10-CM is recorded as Q87.8^[17].
• 3MC syndrome's GARD rare disease ID is recorded as 1118^[18].
• 3MC syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[19].
• 3MC syndrome's Mondo ID is recorded as MONDO_0017398^[20].