Symptom Information: Sort according to HPO 

1
(HPO:0001561) Polyhydramnios 191 / 7739
2
(OMIM) Chorionic lactogen receptor defect 1 / 7739
3
(OMIM) Normal specific insulin binding 1 / 7739
4
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739