Bartter disease type 5
Bartter disease that has material basis in mutation in the MAGED2 gene on chromosome Xp11
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Bartter disease type 5
Summary
Bartter disease type 5 is a class of disease[1].
Key Facts
- Bartter disease type 5's instance of is recorded as class of disease[2].
- Bartter disease type 5's subclass of is recorded as Bartter disease[3].
- Bartter disease type 5's OMIM ID is recorded as 300971[4].
- Bartter disease type 5's Disease Ontology ID is recorded as DOID:0110147[5].
- Bartter disease type 5's genetic association is recorded as MAGED2[6].
- Bartter disease type 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110147[7].
- Bartter disease type 5's exact match is recorded as http://identifiers.org/doid/DOID:0110147[8].
- Bartter disease type 5's UMLS CUI is recorded as C4310820[9].
- Bartter disease type 5's ICD-10-CM is recorded as E26.8[10].
- Bartter disease type 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- Bartter disease type 5's Mondo ID is recorded as MONDO_0010503[12].
- Bartter disease type 5's UniProt disease ID is recorded as DI-04715[13].