Symptom Information: Sort according to HPO 

1
(HPO:0000478) Abnormality of the eye 126 / 7739
2
(HPO:0001249) Intellectual disability 1089 / 7739
3
(HPO:0003080) Hydroxyprolinuria 7 / 7739
4
(HPO:0003108) Hyperglycinuria 11 / 7739
5
(HPO:0003137) Prolinuria 4 / 7739
6
(OMIM) Gyrate atrophy of choroid and retina 1 / 7739
7
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739