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DOID:0110145 - Bartter disease type 4a
Disease Ontology Definition:A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32.
Synonyms: BARTS4A, BSND, Bartter syndrome type 4a , neonatal Bartter syndrome with sensorineural deafness,
Echinobase Genes :
MIM:602522 - bartter syndrome, type 4a |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
Bartter disease (is_a)