OBO ID: DOID:0110145
Term Name: Bartter disease type 4a Search Ontology:
Synonyms:
  • BARTS4A
  • Bartter syndrome type 4a
  • BSND
  • neonatal Bartter syndrome with sensorineural deafness
Definition: A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32. https://www.ncbi.nlm.nih.gov/pubmed/11687798
References:
Ontology: Human Disease   ( DOID:0110145 )
Relationships
is a type of:
OTHER Bartter disease type 4a PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
BSND Sensorineural deafness with mild renal dysfunction 602522
Bartter syndrome, type 4a 602522
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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