Disease #05697 (BARTS5 (Bartter syndrome, type 5, antenatal, transient (BARTS5)), OMIM:300971)
Official abbreviation |
BARTS5 |
Name |
Bartter syndrome, type 5, antenatal, transient (BARTS5) |
OMIM ID |
300971 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
MAGED2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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