Galloway-Mowat syndrome 3

Summary

Galloway-Mowat syndrome 3 is a class of disease^[1].

Key Facts

• Galloway-Mowat syndrome 3's instance of is recorded as class of disease^[2].
• Galloway-Mowat syndrome 3's subclass of is recorded as Galloway-Mowat syndrome^[3].
• Galloway-Mowat syndrome 3's subclass of is recorded as autosomal recessive disease^[4].
• Galloway-Mowat syndrome 3's OMIM ID is recorded as 617729^[5].
• Galloway-Mowat syndrome 3's Disease Ontology ID is recorded as DOID:0080245^[6].
• Galloway-Mowat syndrome 3's Orphanet ID is recorded as 2065^[7].
• Galloway-Mowat syndrome 3's genetic association is recorded as OSGEP^[8].
• Galloway-Mowat syndrome 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080245^[9].
• Galloway-Mowat syndrome 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2065^[10].
• Galloway-Mowat syndrome 3's exact match is recorded as http://identifiers.org/doid/DOID:0080245^[11].
• Galloway-Mowat syndrome 3's UMLS CUI is recorded as C4540266^[12].
• Galloway-Mowat syndrome 3's on focus list of Wikimedia project is recorded as WikiProject Medicine^[13].
• Galloway-Mowat syndrome 3's Mondo ID is recorded as MONDO_0033007^[14].
• Galloway-Mowat syndrome 3's UniProt disease ID is recorded as DI-05106^[15].