Bartter disease type 2
Bartter disease that has material basis in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24
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Bartter disease type 2
Summary
Bartter disease type 2 is a class of disease[1].
Key Facts
- Bartter disease type 2's instance of is recorded as class of disease[2].
- Bartter disease type 2's subclass of is recorded as Bartter disease[3].
- Bartter disease type 2's MeSH descriptor ID is recorded as C537651[4].
- Bartter disease type 2's OMIM ID is recorded as 241200[5].
- Bartter disease type 2's Disease Ontology ID is recorded as DOID:0110143[6].
- Bartter disease type 2's genetic association is recorded as KCNJ1[7].
- Bartter disease type 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110143[8].
- Bartter disease type 2's exact match is recorded as http://identifiers.org/doid/DOID:0110143[9].
- Bartter disease type 2's UMLS CUI is recorded as C1855849[10].
- Bartter disease type 2's ICD-10-CM is recorded as E26.8[11].
- Bartter disease type 2's GARD rare disease ID is recorded as 9658[12].
- Bartter disease type 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Bartter disease type 2's Mondo ID is recorded as MONDO_0009424[14].