|
OMIM |
Link |
Information gain |
01 |
|
epiphyseal dysplasia, microcephaly, and nystagmus
|
[NCBI]
|
0.003449
|
|
|
metaphyseal acroscyphodysplasia
|
[NCBI]
|
0.00278389
|
|
|
spondyloepiphyseal dysplasia tarda, autosomal dominant
|
[NCBI]
|
0.00235593
|
|
|
osteoarthropathy of fingers, familial
|
[NCBI]
|
0.00203025
|
|
|
trichoscyphodysplasia
|
[NCBI]
|
0.00107278
|
|
|
SEMDJL
|
[NCBI]
|
0.000955856
|
|
|
spondylometaphyseal dysplasia, kozlowski type
|
[NCBI]
|
0.000955856
|
|
|
epiphyseal dysplasia, multiple, with early-onset diabetes mellitus
|
[NCBI]
|
0.000804332
|
|
|
PSACH
|
[NCBI]
|
0.000754549
|
|
|
hypertension with brachydactyly
|
[NCBI]
|
0.000710324
|
|
|
EDM1
|
[NCBI]
|
0.000546258
|
|
|
OD
|
[NCBI]
|
0.00048029
|
|
|
renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia
|
[NCBI]
|
0.00047583
|
|
|
ATD1
|
[NCBI]
|
0.000405938
|
|
|
TRPS2
|
[NCBI]
|
0.00039517
|
|
|
fitzsimmons-guilbert syndrome
|
[NCBI]
|
0.000380274
|
|
|
TRPS1
|
[NCBI]
|
0.000319445
|
|
|
RCDP1
|
[NCBI]
|
0.00028999
|
|
|
OSMED
|
[NCBI]
|
0.000272206
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
0.000238769
|
|
|
multiple epiphyseal dysplasia with robin phenotype
|
[NCBI]
|
0.000189909
|
|
|
ASPED
|
[NCBI]
|
0.000189909
|
|
|
symphalangism of toes
|
[NCBI]
|
0.000189909
|
|
|
epiphyseal dysplasia of femoral head, myopia, and deafness
|
[NCBI]
|
0.000189909
|
|
|
macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance
|
[NCBI]
|
0.000189909
|
|
|
spondyloepimetaphyseal dysplasia, micromelic
|
[NCBI]
|
0.000189909
|
|
|
megaepiphyseal dwarfism
|
[NCBI]
|
0.000189909
|
|
|
satoyoshi syndrome
|
[NCBI]
|
0.000189909
|
|
|
SRS
|
[NCBI]
|
0.000185453
|
|
|
RA
|
[NCBI]
|
0.000173963
|
|
|
morquio syndrome, nonkeratosulfate-excreting type
|
[NCBI]
|
0.000150666
|
|
|
ACFD
|
[NCBI]
|
0.000150666
|
|
|
growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction
|
[NCBI]
|
0.000150666
|
|
|
puerto rican infant hypotonia syndrome
|
[NCBI]
|
0.000150666
|
|
|
lissencephaly type iii and bone dysplasia
|
[NCBI]
|
0.000135876
|
|
|
legg-calve-perthes disease
|
[NCBI]
|
0.000126283
|
|
|
EDM4
|
[NCBI]
|
0.000119159
|
|
|
hunter-mcalpine craniosynostosis syndrome
|
[NCBI]
|
0.000119159
|
|
|
schneckenbecken dysplasia
|
[NCBI]
|
0.000119159
|
|
|
EIF2AK3
|
[NCBI]
|
8.9295e-05
|
|
|
SLSN1
|
[NCBI]
|
8.27066e-05
|
|
|
PPAC
|
[NCBI]
|
8.27066e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
7.53781e-05
|
|
|
mucopolysaccharidosis type vii
|
[NCBI]
|
7.41243e-05
|
|
|
ehlers-danlos syndrome, type iv, autosomal dominant
|
[NCBI]
|
7.41243e-05
|
|
|
EVC
|
[NCBI]
|
7.06812e-05
|
|
|
PTH
|
[NCBI]
|
6.52067e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
6.40499e-05
|
|
|
CRMO
|
[NCBI]
|
5.87648e-05
|
|
|
brain-specific homeobox, mouse, homolog of
|
[NCBI]
|
5.33205e-05
|
|
|
SDS
|
[NCBI]
|
5.2184e-05
|
|
|
CHH
|
[NCBI]
|
5.1663e-05
|
|
|
AHO
|
[NCBI]
|
5.11526e-05
|
|
|
DSPG3
|
[NCBI]
|
4.95533e-05
|
|
|
SLC35D1
|
[NCBI]
|
4.95533e-05
|
|
|
ACH
|
[NCBI]
|
4.45505e-05
|
|
|
COL9A2
|
[NCBI]
|
4.38397e-05
|
|
|
BHLHB2
|
[NCBI]
|
4.26348e-05
|
|
|
TRPS1
|
[NCBI]
|
4.16036e-05
|
|
|
PAX4
|
[NCBI]
|
4.07021e-05
|
|
|
MATN3
|
[NCBI]
|
3.99013e-05
|
|
|
PAPSS2
|
[NCBI]
|
3.9181e-05
|
|
|
COL11A2
|
[NCBI]
|
3.85265e-05
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
3.28048e-05
|
|
|
AIS
|
[NCBI]
|
3.14173e-05
|
|
|
COMP
|
[NCBI]
|
1.79704e-05
|
|
|
PCNA
|
[NCBI]
|
1.1776e-05
|
|
|
ACP5
|
[NCBI]
|
1.07406e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
9.60055e-06
|
|
|
SPP1
|
[NCBI]
|
8.35811e-06
|
|
|
VEGF
|
[NCBI]
|
6.93344e-06
|
|
|
PWS
|
[NCBI]
|
4.77234e-06
|
|
|
AR
|
[NCBI]
|
3.29758e-06
|
|
|
AVP
|
[NCBI]
|
1.53669e-06
|
|
|
TH
|
[NCBI]
|
8.28203e-07
|
|
|
NPY
|
[NCBI]
|
5.33436e-07
|
|
|
EGF
|
[NCBI]
|
4.28196e-07
|
|