|
OMIM |
Link |
Information gain |
01 |
|
omodysplasia, generalized form
|
[NCBI]
|
0.00433624
|
|
|
omodysplasia
|
[NCBI]
|
0.00375529
|
|
|
humeroradial synostosis
|
[NCBI]
|
0.00281988
|
|
|
arthrogryposis-like disorder
|
[NCBI]
|
0.0014006
|
|
|
spondyloepiphyseal dysplasia tarda, autosomal dominant
|
[NCBI]
|
0.00097306
|
|
|
epiphyseal dysplasia, microcephaly, and nystagmus
|
[NCBI]
|
0.000840987
|
|
|
humerospinal dysostosis
|
[NCBI]
|
0.000770094
|
|
|
kyphomelic dysplasia
|
[NCBI]
|
0.000699657
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.000675099
|
|
|
OSCS
|
[NCBI]
|
0.000633045
|
|
|
ABS
|
[NCBI]
|
0.00050038
|
|
|
SPMM
|
[NCBI]
|
0.000441506
|
|
|
humeroradial synostosis
|
[NCBI]
|
0.000384054
|
|
|
rhizomelic dysplasia, patterson-lowry type
|
[NCBI]
|
0.000329983
|
|
|
rhizomelic syndrome
|
[NCBI]
|
0.000329983
|
|
|
AOI
|
[NCBI]
|
0.000249204
|
|
|
MAS
|
[NCBI]
|
0.000233019
|
|
|
camurati-engelmann disease
|
[NCBI]
|
0.000217584
|
|
|
chondrosarcoma
|
[NCBI]
|
0.000191783
|
|
|
lethal short-limb skeletal dysplasia, al gazali type
|
[NCBI]
|
0.000191783
|
|
|
ribbing disease
|
[NCBI]
|
0.000191783
|
|
|
CRMO
|
[NCBI]
|
0.000160282
|
|
|
micromelic dysplasia, congenital, with dislocation of radius
|
[NCBI]
|
0.000152538
|
|
|
renal dysplasia-limb defects syndrome
|
[NCBI]
|
0.000152538
|
|
|
prenatal bowing
|
[NCBI]
|
0.000152538
|
|
|
melorheostosis
|
[NCBI]
|
0.000137745
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
0.000137745
|
|
|
caffey disease
|
[NCBI]
|
0.000115351
|
|
|
aglossia-adactylia
|
[NCBI]
|
0.000115351
|
|
|
bowing of legs, anterior, with dwarfism
|
[NCBI]
|
0.000115351
|
|
|
osteogenic sarcoma
|
[NCBI]
|
0.00010661
|
|
|
scapuloperoneal syndrome, neurogenic, kaeser type
|
[NCBI]
|
0.000103091
|
|
|
RNS
|
[NCBI]
|
0.000103091
|
|
|
buschke-ollendorff syndrome
|
[NCBI]
|
9.99691e-05
|
|
|
acheiropody
|
[NCBI]
|
9.71634e-05
|
|
|
exostoses, multiple, type ii
|
[NCBI]
|
9.71634e-05
|
|
|
diastrophic dysplasia
|
[NCBI]
|
9.71634e-05
|
|
|
pulmonary alveolar microlithiasis
|
[NCBI]
|
9.46165e-05
|
|
|
DMC
|
[NCBI]
|
9.46165e-05
|
|
|
paget disease, juvenile
|
[NCBI]
|
9.46165e-05
|
|
|
CIPA
|
[NCBI]
|
9.2285e-05
|
|
|
plasmin inhibitor deficiency
|
[NCBI]
|
9.08171e-05
|
|
|
FMD
|
[NCBI]
|
9.01357e-05
|
|
|
EDMD2
|
[NCBI]
|
8.81425e-05
|
|
|
PTH
|
[NCBI]
|
8.40897e-05
|
|
|
CCAL2
|
[NCBI]
|
8.29096e-05
|
|
|
IHH
|
[NCBI]
|
8.09333e-05
|
|
|
HFTC
|
[NCBI]
|
7.99075e-05
|
|
|
SEDC
|
[NCBI]
|
7.99075e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
7.72052e-05
|
|
|
SLE
|
[NCBI]
|
7.57174e-05
|
|
|
HSAN3
|
[NCBI]
|
6.94447e-05
|
|
|
RCDP1
|
[NCBI]
|
6.67057e-05
|
|
|
ACP5
|
[NCBI]
|
5.53942e-05
|
|
|
AHO
|
[NCBI]
|
5.29106e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
5.17133e-05
|
|
|
COMP
|
[NCBI]
|
4.597e-05
|
|
|
FAM20C
|
[NCBI]
|
4.38397e-05
|
|
|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency
|
[NCBI]
|
4.13877e-05
|
|
|
farber lipogranulomatosis
|
[NCBI]
|
3.9181e-05
|
|
|
EXT2
|
[NCBI]
|
3.85265e-05
|
|
|
PAX1
|
[NCBI]
|
3.85265e-05
|
|
|
EXT1
|
[NCBI]
|
3.68595e-05
|
|
|
COL10A1
|
[NCBI]
|
3.68595e-05
|
|
|
PTHR1
|
[NCBI]
|
3.25289e-05
|
|
|
RUNX2
|
[NCBI]
|
3.08482e-05
|
|
|
TNFRSF1A
|
[NCBI]
|
2.50413e-05
|
|
|
RA
|
[NCBI]
|
2.3629e-05
|
|
|
FGFR2
|
[NCBI]
|
2.30793e-05
|
|
|
ABCC1
|
[NCBI]
|
1.35817e-05
|
|
|
CTGF
|
[NCBI]
|
1.1682e-05
|
|
|
SPP1
|
[NCBI]
|
8.35811e-06
|
|
|
EPO
|
[NCBI]
|
2.83473e-06
|
|
|
VEGF
|
[NCBI]
|
1.68173e-07
|
|