Meckel syndrome 13

Summary

Meckel syndrome 13 is a class of disease^[1].

Key Facts

• Meckel syndrome 13's instance of is recorded as class of disease^[2].
• Meckel syndrome 13's subclass of is recorded as Meckel syndrome^[3].
• Meckel syndrome 13's subclass of is recorded as autosomal recessive disease^[4].
• Meckel syndrome 13's OMIM ID is recorded as 617562^[5].
• Meckel syndrome 13's Disease Ontology ID is recorded as DOID:0080253^[6].
• Meckel syndrome 13's Orphanet ID is recorded as 564^[7].
• Meckel syndrome 13's genetic association is recorded as TMEM107^[8].
• Meckel syndrome 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080253^[9].
• Meckel syndrome 13's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_564^[10].
• Meckel syndrome 13's exact match is recorded as http://identifiers.org/doid/DOID:0080253^[11].
• Meckel syndrome 13's UMLS CUI is recorded as C4539715^[12].
• Meckel syndrome 13's UMLS CUI is recorded as C4539714^[13].
• Meckel syndrome 13's on focus list of Wikimedia project is recorded as WikiProject Medicine^[14].
• Meckel syndrome 13's Mondo ID is recorded as MONDO_0033044^[15].
• Meckel syndrome 13's UniProt disease ID is recorded as DI-05035^[16].