Symptom Information: Sort according to HPO 

1
(HPO:0000545) Myopia Very frequent [Orphanet] 286 / 7739
2
(HPO:0001162) Postaxial hand polydactyly Very frequent [Orphanet] 119 / 7739
3
(HPO:0004299) Hernia of the abdominal wall Frequent [Orphanet] 176 / 7739
4
(HPO:0100259) Postaxial polydactyly 85 / 7739
5
(OMIM) Progressive myopia 1 / 7739
6
(HPO:0000035) Abnormality of the testis Frequent [Orphanet] 296 / 7739
7
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739