(Q27674850)
English
Bartter disease type 4a
A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32.
- BARTS4A
- BSND
- Bartter syndrome type 4a
- neonatal Bartter syndrome with sensorineural deafness
- BARTTER SYNDROME, TYPE 4A
- Bartter Syndrome, Infantile, With Sensorineural Deafness
- Sensorineural Deafness With Mild Renal Dysfunction
Statements
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Identifiers
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