Branchio-oto-renal syndrome type 2
GPTKB entity
Statements (13)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
|
| gptkbp:alternativeName |
BOR2
|
| gptkbp:associatedWith |
unknown (gene not identified)
|
| https://www.w3.org/2000/01/rdf-schema#label |
Branchio-oto-renal syndrome type 2
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:OMIM |
610896
|
| gptkbp:subspecies |
gptkb:Branchio-oto-renal_syndrome
|
| gptkbp:symptom |
hearing loss
renal anomalies preauricular pits branchial cleft anomalies |
| gptkbp:bfsParent |
gptkb:SIX5
|
| gptkbp:bfsLayer |
8
|