|
OMIM |
Link |
Information
gain |
01 |
|
|
hairy elbows
|
[NCBI]
|
0.00982405
|
|
|
|
arthrogryposis-like disorder
|
[NCBI]
|
0.00135232
|
|
|
|
pterygium, antecubital
|
[NCBI]
|
0.00104185
|
|
|
|
synostosis, carpal, with dysplastic elbow joints and brachydactyly
|
[NCBI]
|
0.00104185
|
|
|
|
VDEGS
|
[NCBI]
|
0.000849287
|
|
|
|
omodysplasia
|
[NCBI]
|
0.000849287
|
|
|
|
popliteal pterygium syndrome, lethal type
|
[NCBI]
|
0.000793129
|
|
|
|
epiphyseal dysplasia, microcephaly, and nystagmus
|
[NCBI]
|
0.000793129
|
|
|
|
migraine with or without aura, susceptibility to, 1
|
[NCBI]
|
0.000711442
|
|
|
|
omodysplasia, generalized form
|
[NCBI]
|
0.000652218
|
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.000627765
|
|
|
|
NPS
|
[NCBI]
|
0.000467576
|
|
|
|
pena-shokeir syndrome, type i
|
[NCBI]
|
0.0003912
|
|
|
|
HFTC
|
[NCBI]
|
0.000237499
|
|
|
|
dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation
|
[NCBI]
|
0.000210237
|
|
|
|
micromelic dysplasia, congenital, with dislocation of radius
|
[NCBI]
|
0.000170976
|
|
|
|
genu valgum, st. helena familial
|
[NCBI]
|
0.000170976
|
|
|
|
poikiloderma, hereditary sclerosing
|
[NCBI]
|
0.000170976
|
|
|
|
S PEAK SYNDROME
|
[NCBI]
|
0.000170976
|
|
|
|
mental retardation syndrome, mietens-weber type
|
[NCBI]
|
0.000170976
|
|
|
|
chondrocalcinosis due to apatite crystal deposition
|
[NCBI]
|
0.000170976
|
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
0.000156168
|
|
|
|
HHS
|
[NCBI]
|
0.000156168
|
|
|
|
ODG2
|
[NCBI]
|
0.000133727
|
|
|
|
cleft lip/palate with abnormal thumbs and microcephaly
|
[NCBI]
|
0.000133727
|
|
|
|
fibromatosis, juvenile hyaline
|
[NCBI]
|
0.000124955
|
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
0.000118283
|
|
|
|
multiple pterygium syndrome, escobar variant
|
[NCBI]
|
0.000118283
|
|
|
|
SYM1
|
[NCBI]
|
0.000108387
|
|
|
|
cerebrocostomandibular syndrome
|
[NCBI]
|
0.000108387
|
|
|
|
MB
|
[NCBI]
|
0.000106556
|
|
|
|
CCAL2
|
[NCBI]
|
0.000101098
|
|
|
|
LWD
|
[NCBI]
|
8.55735e-05
|
|
|
|
RDT
|
[NCBI]
|
7.51038e-05
|
|
|
|
HOS
|
[NCBI]
|
7.27319e-05
|
|
|
|
contractural arachnodactyly, congenital
|
[NCBI]
|
4.39208e-05
|
|
|
|
CALCA
|
[NCBI]
|
4.35608e-05
|
|
|
|
FGFR2
|
[NCBI]
|
3.22061e-05
|
|
|
|
MUC1
|
[NCBI]
|
2.15579e-05
|
|
|
|
CEACAM5
|
[NCBI]
|
1.15647e-05
|
|
|
|
CF
|
[NCBI]
|
1.14567e-05
|
|
|
|
VIP
|
[NCBI]
|
8.29821e-06
|
|
|
|
TH
|
[NCBI]
|
6.9488e-06
|
|
|
|
NPY
|
[NCBI]
|
6.29553e-06
|
|
|
|
MG
|
[NCBI]
|
5.22237e-06
|
|
|
|
RA
|
[NCBI]
|
3.92955e-07
|
|
