Bartter disease type 4b Disease Ontology Browser

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Disease Ontology Browser

Bartter disease type 4b (DOID:0110146)
Alliance: disease page
Synonyms: BARTS4B; Bartter syndrome, type 4b, digenic; neonatal Bartter syndrome type 4B with sensorineural deafness
Alt IDs: OMIM:613090, ICD10CM:E26.8
Definition: A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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