Bartter disease type 3
Bartter disease that has material basis in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36
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Bartter disease type 3
Summary
Bartter disease type 3 is a rare disease[1].
Key Facts
- Bartter disease type 3's instance of is recorded as rare disease[2].
- Bartter disease type 3's instance of is recorded as class of disease[3].
- Bartter disease type 3's subclass of is recorded as Bartter disease[4].
- Bartter disease type 3's OMIM ID is recorded as 607364[5].
- Bartter disease type 3's Disease Ontology ID is recorded as DOID:0110144[6].
- Bartter disease type 3's Orphanet ID is recorded as 93605[7].
- Bartter disease type 3's genetic association is recorded as CLCNKB[8].
- Bartter disease type 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110144[9].
- Bartter disease type 3's exact match is recorded as http://identifiers.org/doid/DOID:0110144[10].
- Bartter disease type 3's UMLS CUI is recorded as C1846343[11].
- Bartter disease type 3's UMLS CUI is recorded as C1846344[12].
- Bartter disease type 3's ICD-10-CM is recorded as E26.8[13].
- Bartter disease type 3's GARD rare disease ID is recorded as 9659[14].
- Bartter disease type 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Bartter disease type 3's Mondo ID is recorded as MONDO_0011822[16].
- Bartter disease type 3's UniProt disease ID is recorded as DI-00175[17].