Síndrome de anomalías congénitas del riñón y del tracto urinario asociado a PBX1
ORPHA:656130· ICD-10 Q87.8· PBX1-related congenital anomalies of kidney-urinary tract syndrome
- Herencia
- Autosomal dominant
ORPHA:656130· ICD-10 Q87.8· PBX1-related congenital anomalies of kidney-urinary tract syndrome