Symptom Information: Sort according to HPO 

1
(HPO:0001852) Sandal gap Very frequent [Orphanet] 63 / 7739
2
(HPO:0004209) Clinodactyly of the 5th finger Frequent [Orphanet] 288 / 7739
3
(HPO:0001159) Syndactyly 140 / 7739
4
(HPO:0001177) Preaxial hand polydactyly 59 / 7739
5
(HPO:0008080) Hallux varus 3 / 7739
6
(HPO:0010055) Broad hallux 56 / 7739
7
(OMIM) Preaxial polysyndactyly 2 / 7739
8
(OMIM) Duplication or triplication of phalanges 1 / 7739
9
(HPO:0000007) Autosomal recessive inheritance 2538 / 7739