Symptom Information: Sort according to HPO 

1
 (HPO:0001263) Global developmental delay 853 / 7739
2
 (HPO:0002135) Basal ganglia calcification 37 / 7739
3
 (HPO:0002415) Leukodystrophy 30 / 7739
4
 (HPO:0008872) Feeding difficulties in infancy 153 / 7739
5
 (HPO:0009710) Chilblain lesions 3 / 7739
6
 (HPO:0000007) Autosomal recessive inheritance 2538 / 7739