1
|
(HPO:0011305)
|
Partial absence of toe |
Very frequent [Orphanet]
|
|
|
|
18 / 7739
|
2
|
(HPO:0009700)
|
Finger symphalangism |
Frequent [Orphanet]
|
|
|
|
55 / 7739
|
3
|
(HPO:0004279)
|
Short palm |
Very frequent [Orphanet]
|
|
|
|
323 / 7739
|
4
|
(HPO:0004209)
|
Clinodactyly of the 5th finger |
Frequent [Orphanet]
|
|
|
|
288 / 7739
|
5
|
(HPO:0005048)
|
Synostosis of carpal bones |
Frequent [Orphanet]
|
|
|
|
39 / 7739
|
6
|
(HPO:0001770)
|
Toe syndactyly |
Very frequent [Orphanet]
|
|
|
|
149 / 7739
|
7
|
(HPO:0009776)
|
Adactyly |
Very frequent [Orphanet]
|
|
|
|
11 / 7739
|
8
|
(HPO:0010109)
|
Short hallux |
Very frequent [Orphanet]
|
|
|
|
27 / 7739
|
9
|
(HPO:0009601)
|
Aplasia/Hypoplasia of the thumb |
Very frequent [Orphanet]
|
|
|
|
80 / 7739
|
10
|
(HPO:0000954)
|
Single transverse palmar crease |
|
|
|
|
162 / 7739
|
11
|
(HPO:0001163)
|
Abnormality of the metacarpal bones |
Very frequent [Orphanet]
|
|
|
|
149 / 7739
|
12
|
(HPO:0006097)
|
3-4 finger syndactyly |
|
|
|
|
7 / 7739
|
13
|
(HPO:0008362)
|
Aplasia/Hypoplasia of the hallux |
|
|
|
|
4 / 7739
|
14
|
(HPO:0009161)
|
Aplasia/Hypoplasia of the middle phalanx of the 5th finger |
|
|
|
|
4 / 7739
|
15
|
(HPO:0009177)
|
Proximal/middle symphalangism of 5th finger |
|
|
|
|
4 / 7739
|
16
|
(HPO:0009568)
|
Aplasia/Hypoplasia of the middle phalanx of the 2nd finger |
|
|
|
|
4 / 7739
|
17
|
(HPO:0010064)
|
Symphalangism affecting the phalanges of the hallux |
|
|
|
|
1 / 7739
|
18
|
(OMIM)
|
Four fingers on each hand |
|
|
|
|
1 / 7739
|
19
|
(OMIM)
|
Bilateral transverse palmar creases |
|
|
|
|
4 / 7739
|
20
|
(OMIM)
|
Complete syndactyly/synostosis of 3rd-4th fingers |
|
|
|
|
1 / 7739
|
21
|
(OMIM)
|
Aplasia/hypoplasia of middle phalanges of 2nd and 5th fingers |
|
|
|
|
1 / 7739
|
22
|
(OMIM)
|
Aplasia/hypoplasia of halluces |
|
|
|
|
1 / 7739
|
23
|
(OMIM)
|
Complete or partial syndactyly |
|
|
|
|
1 / 7739
|
24
|
(OMIM)
|
Hypoplasia of distal and middle phalanges |
|
|
|
|
1 / 7739
|
25
|
(HPO:0006101)
|
Finger syndactyly |
Very frequent [Orphanet]
|
|
|
|
198 / 7739
|
26
|
(HPO:0000007)
|
Autosomal recessive inheritance |
|
|
|
|
2538 / 7739
|