Galloway-Mowat syndrome 2
human disease
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Summary
Galloway-Mowat syndrome 2 is a class of disease[1].
Key Facts
- Galloway-Mowat syndrome 2's instance of is recorded as class of disease[2].
- Galloway-Mowat syndrome 2's subclass of is recorded as Galloway-Mowat syndrome[3].
- Galloway-Mowat syndrome 2's subclass of is recorded as X-linked recessive disease[4].
- Galloway-Mowat syndrome 2's OMIM ID is recorded as 301006[5].
- Galloway-Mowat syndrome 2's Disease Ontology ID is recorded as DOID:0080244[6].
- Galloway-Mowat syndrome 2's Orphanet ID is recorded as 2065[7].
- Galloway-Mowat syndrome 2's genetic association is recorded as LAGE3[8].
- Galloway-Mowat syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080244[9].
- Galloway-Mowat syndrome 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2065[10].
- Galloway-Mowat syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0080244[11].
- Galloway-Mowat syndrome 2's UMLS CUI is recorded as C4538784[12].
- Galloway-Mowat syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Galloway-Mowat syndrome 2's Mondo ID is recorded as MONDO_0033006[14].
- Galloway-Mowat syndrome 2's UniProt disease ID is recorded as DI-05105[15].