Human genes for Meckel syndrome
Meckel syndrome [DOID:0050778]
A ciliopathy that is characterized by renal cystic dysplasia, occipital encephalocele, polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia.
Synonyms: Meckel syndrome, DOID:0050778, Meckel disease, Meckel disorder, Meckel syndromes ...
Linkouts: OMIM