Disease #05697 (BARTS5 (syndrome, Bartter, type 5, antenatal, transient (BARTS5)), OMIM:300971)

Official abbreviation BARTS5
Name syndrome, Bartter, type 5, antenatal, transient (BARTS5)
OMIM ID 300971
Human Phenotype Ontology Project (HPO) HPO
Inheritance XLR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MAGED2
Associated tissues -
Disease features -
Remarks -