Symptom Information: Sort according to HPO 

1
(HPO:0000252) Microcephaly 832 / 7739
2
(HPO:0001159) Syndactyly 140 / 7739
3
(HPO:0001249) Intellectual disability 1089 / 7739
4
(HPO:0007269) Spinal muscular atrophy 24 / 7739
5
(HPO:0003202) Skeletal muscle atrophy 281 / 7739
6
(OMIM) Mitten-like syndactyly 1 / 7739
7
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739