Syndrome d'anomalies congénitales du rein et des voies urinaires associé à PBX1
ORPHA:656130· ICD-10 Q87.8· PBX1-related congenital anomalies of kidney-urinary tract syndrome
- Transmission
- Autosomal dominant
ORPHA:656130· ICD-10 Q87.8· PBX1-related congenital anomalies of kidney-urinary tract syndrome