Bartter disease type 4a
Bartter disease that has material basis in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32
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Bartter disease type 4a
Summary
Bartter disease type 4a is a rare disease[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- Bartter disease type 4a's instance of is recorded as rare disease[3].
- Bartter disease type 4a's instance of is recorded as class of disease[4].
- Bartter disease type 4a is a type of Bartter disease[5].
- Bartter disease type 4a is a type of infantile Bartter syndrome with sensorineural deafness[6].
- Bartter disease type 4a's genetic association is recorded as BSND[7].
- Bartter disease type 4a's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110145[8].
- Bartter disease type 4a's exact match is recorded as http://identifiers.org/doid/DOID:0110145[9].
- Bartter disease type 4a's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
Bartter disease type 4a is known by 8 alternative names across languages and contexts.[2]