Symptom Information: Sort according to HPO 

1
(HPO:0001249) Intellectual disability 1089 / 7739
2
(HPO:0001510) Growth delay 295 / 7739
3
(HPO:0003297) Hyperlysinuria 10 / 7739
4
(HPO:0008272) Renal tubular lysine transport defect 1 / 7739
5
(OMIM) Low serum lysine 1 / 7739
6
(OMIM) Impaired lysine intestinal absorption 1 / 7739
7
(OMIM) Intestinal lysine transport defect 1 / 7739
8
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739