Disease-gene associations mined from literature

Human genes for acrorenal syndrome

Acrorenal syndrome [DOID:0060347]

A syndrome characterized by limb defects, usually bilateral, like cleft hands or feet and longitudinal defects involving radius or ulna, tibia or fibula and renal anomalies which include agenesis, hypoplasia and rarely polycystic kidneys. Additional malformations may involve the oro-mandibular region, the trachea and lungs, skin derivatives including sweat glands, mammary glands, the uterus, vas deferens, the nasal placodes and the eyes.

Synonyms:  acrorenal syndrome,  DOID:0060347,  acrorenal disease,  acrorenal disorder,  acrorenal syndromes