Galloway-Mowat syndrome 5
human disease
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Summary
Galloway-Mowat syndrome 5 is a class of disease[1].
Key Facts
- Galloway-Mowat syndrome 5's instance of is recorded as class of disease[2].
- Galloway-Mowat syndrome 5's subclass of is recorded as Galloway-Mowat syndrome[3].
- Galloway-Mowat syndrome 5's OMIM ID is recorded as 617731[4].
- Galloway-Mowat syndrome 5's Disease Ontology ID is recorded as DOID:0080247[5].
- Galloway-Mowat syndrome 5's Orphanet ID is recorded as 2065[6].
- Galloway-Mowat syndrome 5's genetic association is recorded as TPRKB[7].
- Galloway-Mowat syndrome 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080247[8].
- Galloway-Mowat syndrome 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2065[9].
- Galloway-Mowat syndrome 5's exact match is recorded as http://identifiers.org/doid/DOID:0080247[10].
- Galloway-Mowat syndrome 5's UMLS CUI is recorded as C4540274[11].
- Galloway-Mowat syndrome 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- Galloway-Mowat syndrome 5's Mondo ID is recorded as MONDO_0033009[13].
- Galloway-Mowat syndrome 5's UniProt disease ID is recorded as DI-05108[14].