|
OMIM |
Link |
Information gain |
01 |
|
RA
|
[NCBI]
|
0.0044413
|
|
|
acroosteolysis with osteoporosis and changes in skull and mandible
|
[NCBI]
|
0.00204182
|
|
|
amyotrophy, monomelic
|
[NCBI]
|
0.00195814
|
|
|
mohr syndrome
|
[NCBI]
|
0.00195814
|
|
|
CTS1
|
[NCBI]
|
0.00188416
|
|
|
upington disease
|
[NCBI]
|
0.00110106
|
|
|
spondylometaphyseal dysplasia, type a4
|
[NCBI]
|
0.00110106
|
|
|
brachydactyly, type a5, with nail dysplasia
|
[NCBI]
|
0.00110106
|
|
|
SHFLD1
|
[NCBI]
|
0.00105133
|
|
|
fingerprints, absence of
|
[NCBI]
|
0.000791708
|
|
|
dermal ridges-off-the-end
|
[NCBI]
|
0.000791708
|
|
|
osteodysplasia, familial, anderson type
|
[NCBI]
|
0.000791708
|
|
|
MPD3
|
[NCBI]
|
0.000791708
|
|
|
dyschromatosis universalis hereditaria
|
[NCBI]
|
0.000791708
|
|
|
clubbing of digits
|
[NCBI]
|
0.000791708
|
|
|
MF4
|
[NCBI]
|
0.000675971
|
|
|
spondylometaphyseal dysplasia, corner fracture type
|
[NCBI]
|
0.000675971
|
|
|
epidermolysis bullosa inversa dystrophica
|
[NCBI]
|
0.000675971
|
|
|
spondyloepiphyseal dysplasia tarda, autosomal dominant
|
[NCBI]
|
0.000675971
|
|
|
SHFM1
|
[NCBI]
|
0.000647829
|
|
|
CF
|
[NCBI]
|
0.000618253
|
|
|
keratolytic winter erythema
|
[NCBI]
|
0.000601389
|
|
|
dupuytren contracture
|
[NCBI]
|
0.000601389
|
|
|
brachydactyly-mental retardation syndrome
|
[NCBI]
|
0.000601389
|
|
|
SHFM2
|
[NCBI]
|
0.000601389
|
|
|
dermal ridges, patternless
|
[NCBI]
|
0.000601389
|
|
|
epiphyseal dysplasia, microcephaly, and nystagmus
|
[NCBI]
|
0.000546353
|
|
|
hereditary motor and sensory neuropathy v
|
[NCBI]
|
0.000502829
|
|
|
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases
|
[NCBI]
|
0.000502829
|
|
|
hand clasping pattern
|
[NCBI]
|
0.000490195
|
|
|
stiff skin syndrome
|
[NCBI]
|
0.000466912
|
|
|
HOA
|
[NCBI]
|
0.000453079
|
|
|
ZLS
|
[NCBI]
|
0.000409934
|
|
|
DBQD
|
[NCBI]
|
0.000386605
|
|
|
WDM
|
[NCBI]
|
0.000386605
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.000386605
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000329941
|
|
|
tetramelic monodactyly
|
[NCBI]
|
0.000280286
|
|
|
HSR
|
[NCBI]
|
0.00024452
|
|
|
proteus syndrome
|
[NCBI]
|
0.000232125
|
|
|
SPD1
|
[NCBI]
|
0.000231166
|
|
|
acrogeria, gottron type
|
[NCBI]
|
0.000226385
|
|
|
osteoarthritis
|
[NCBI]
|
0.000223586
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000219316
|
|
|
renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia
|
[NCBI]
|
0.00018555
|
|
|
EEC1
|
[NCBI]
|
0.000177777
|
|
|
poland syndrome
|
[NCBI]
|
0.000159507
|
|
|
SPG17
|
[NCBI]
|
0.000154036
|
|
|
spondyloepimetaphyseal dysplasia, strudwick type
|
[NCBI]
|
0.000140122
|
|
|
osteolysis, hereditary multicentric
|
[NCBI]
|
0.000140104
|
|
|
metachondromatosis
|
[NCBI]
|
0.000140104
|
|
|
tendons, extensor, of fingers, anomalous insertion of
|
[NCBI]
|
0.000140104
|
|
|
angiolipomatosis, familial
|
[NCBI]
|
0.000140104
|
|
|
dermatoglyphics--palmar triradius d, absence of
|
[NCBI]
|
0.000140104
|
|
|
eiken skeletal dysplasia
|
[NCBI]
|
0.000140104
|
|
|
acrorenal syndrome
|
[NCBI]
|
0.000140104
|
|
|
dermatoglyphics--hypothenar radial arch
|
[NCBI]
|
0.000140104
|
|
|
palmomental reflex
|
[NCBI]
|
0.000140104
|
|
|
adactylia, unilateral
|
[NCBI]
|
0.000140104
|
|
|
symphalangism with multiple anomalies of hands and feet
|
[NCBI]
|
0.000140104
|
|
|
arm folding preference
|
[NCBI]
|
0.000140104
|
|
|
AOS
|
[NCBI]
|
0.000129142
|
|
|
DMC
|
[NCBI]
|
0.000129115
|
|
|
dyschromatosis symmetrica hereditaria 1
|
[NCBI]
|
0.000124374
|
|
|
SYM1
|
[NCBI]
|
0.00012003
|
|
|
LRS1
|
[NCBI]
|
0.00010885
|
|
|
pfeiffer syndrome
|
[NCBI]
|
0.00010885
|
|
|
SLSN1
|
[NCBI]
|
0.00010885
|
|
|
PPAC
|
[NCBI]
|
0.00010885
|
|
|
SLE
|
[NCBI]
|
0.00010823
|
|
|
acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia
|
[NCBI]
|
0.000101029
|
|
|
congenital disorder of glycosylation, type i/iix
|
[NCBI]
|
0.000101029
|
|
|
chondrocalcinosis due to apatite crystal deposition
|
[NCBI]
|
0.000101029
|
|
|
prader-willi habitus, osteopenia, and camptodactyly
|
[NCBI]
|
0.000101029
|
|
|
acrocephalopolydactylous dysplasia
|
[NCBI]
|
0.000101029
|
|
|
spondylometaphyseal dysplasia, east african type
|
[NCBI]
|
0.000101029
|
|
|
achard syndrome
|
[NCBI]
|
0.000101029
|
|
|
fingers, relative length of
|
[NCBI]
|
0.000101029
|
|
|
dermal ridges, nelson syndrome
|
[NCBI]
|
0.000101029
|
|
|
median-ulnar nerve communications
|
[NCBI]
|
0.000101029
|
|
|
ulna metaphyseal dysplasia syndrome
|
[NCBI]
|
0.000101029
|
|
|
puerto rican infant hypotonia syndrome
|
[NCBI]
|
0.000101029
|
|
|
HCH
|
[NCBI]
|
9.97061e-05
|
|
|
SEDC
|
[NCBI]
|
9.97061e-05
|
|
|
COMP
|
[NCBI]
|
9.72586e-05
|
|
|
COL2A1
|
[NCBI]
|
9.56667e-05
|
|
|
MG
|
[NCBI]
|
9.25468e-05
|
|
|
brachydactyly, preaxial, with hallux varus and thumb abduction
|
[NCBI]
|
8.6406e-05
|
|
|
melorheostosis
|
[NCBI]
|
8.6406e-05
|
|
|
ankylosing vertebral hyperostosis with tylosis
|
[NCBI]
|
8.6406e-05
|
|
|
ivic syndrome
|
[NCBI]
|
8.6406e-05
|
|
|
TCC
|
[NCBI]
|
8.6406e-05
|
|
|
SHFM4
|
[NCBI]
|
8.6406e-05
|
|
|
PRTS
|
[NCBI]
|
8.6406e-05
|
|
|
DA2A
|
[NCBI]
|
8.33321e-05
|
|
|
MATN3
|
[NCBI]
|
8.31786e-05
|
|
|
WS3
|
[NCBI]
|
7.69808e-05
|
|
|
roussy-levy hereditary areflexic dystasia
|
[NCBI]
|
7.69808e-05
|
|
|
syndactyly, type iii
|
[NCBI]
|
7.69808e-05
|
|
|
SMC
|
[NCBI]
|
7.00241e-05
|
|
|
EDM4
|
[NCBI]
|
7.00241e-05
|
|
|
spondyloperipheral dysplasia
|
[NCBI]
|
7.00241e-05
|
|
|
BCNS
|
[NCBI]
|
6.93276e-05
|
|
|
enchondromatosis, multiple
|
[NCBI]
|
6.45214e-05
|
|
|
BDE
|
[NCBI]
|
6.45214e-05
|
|
|
DA1
|
[NCBI]
|
6.45214e-05
|
|
|
ruvalcaba syndrome
|
[NCBI]
|
6.45214e-05
|
|
|
palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal
|
[NCBI]
|
6.45214e-05
|
|
|
OSMED
|
[NCBI]
|
6.45214e-05
|
|
|
hyperostosis corticalis generalisata
|
[NCBI]
|
6.45214e-05
|
|
|
KAL1
|
[NCBI]
|
6.24565e-05
|
|
|
marshall-smith syndrome
|
[NCBI]
|
5.99793e-05
|
|
|
TD2
|
[NCBI]
|
5.61201e-05
|
|
|
HOS
|
[NCBI]
|
5.30187e-05
|
|
|
pycnodysostosis
|
[NCBI]
|
5.27714e-05
|
|
|
SDS
|
[NCBI]
|
5.11088e-05
|
|
|
buschke-ollendorff syndrome
|
[NCBI]
|
4.9819e-05
|
|
|
BDB1
|
[NCBI]
|
4.9819e-05
|
|
|
vater association
|
[NCBI]
|
4.9819e-05
|
|
|
PSACH
|
[NCBI]
|
4.92896e-05
|
|
|
diastrophic dysplasia
|
[NCBI]
|
4.71832e-05
|
|
|
OPD1
|
[NCBI]
|
4.71832e-05
|
|
|
hand-foot-uterus syndrome
|
[NCBI]
|
4.71832e-05
|
|
|
SYNS1
|
[NCBI]
|
4.71832e-05
|
|
|
PDP
|
[NCBI]
|
4.71832e-05
|
|
|
BST1
|
[NCBI]
|
4.5782e-05
|
|
|
sitosterolemia
|
[NCBI]
|
4.48062e-05
|
|
|
HSAN2
|
[NCBI]
|
4.48062e-05
|
|
|
CMT1A
|
[NCBI]
|
4.3545e-05
|
|
|
WISP3
|
[NCBI]
|
4.33367e-05
|
|
|
BDC
|
[NCBI]
|
4.26446e-05
|
|
|
SLC39A4
|
[NCBI]
|
4.15188e-05
|
|
|
weaver syndrome
|
[NCBI]
|
4.06652e-05
|
|
|
DRRS
|
[NCBI]
|
4.06652e-05
|
|
|
FMD
|
[NCBI]
|
4.06652e-05
|
|
|
trichodentoosseous syndrome
|
[NCBI]
|
3.88419e-05
|
|
|
chondrodysplasia punctata, autosomal dominant
|
[NCBI]
|
3.88419e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
3.88419e-05
|
|
|
apert syndrome
|
[NCBI]
|
3.88419e-05
|
|
|
CACP
|
[NCBI]
|
3.88419e-05
|
|
|
ADAR
|
[NCBI]
|
3.69353e-05
|
|
|
SLC26A2
|
[NCBI]
|
3.61352e-05
|
|
|
SALL4
|
[NCBI]
|
3.47619e-05
|
|
|
PLOSL
|
[NCBI]
|
3.41187e-05
|
|
|
mucolipidosis iiia
|
[NCBI]
|
3.41187e-05
|
|
|
CCAL2
|
[NCBI]
|
3.41187e-05
|
|
|
MADA
|
[NCBI]
|
3.14565e-05
|
|
|
TP73L
|
[NCBI]
|
3.09721e-05
|
|
|
ARX
|
[NCBI]
|
3.02725e-05
|
|
|
OFD1
|
[NCBI]
|
3.02415e-05
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
2.9094e-05
|
|
|
PTHR1
|
[NCBI]
|
2.87756e-05
|
|
|
EBR1
|
[NCBI]
|
2.80079e-05
|
|
|
TRPS1
|
[NCBI]
|
2.80079e-05
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
2.75399e-05
|
|
|
ACLS
|
[NCBI]
|
2.59993e-05
|
|
|
PD
|
[NCBI]
|
2.59697e-05
|
|
|
PAX3
|
[NCBI]
|
2.41755e-05
|
|
|
MAOA
|
[NCBI]
|
2.38994e-05
|
|
|
GNAS
|
[NCBI]
|
2.37654e-05
|
|
|
LOX
|
[NCBI]
|
2.27764e-05
|
|
|
breast cancer
|
[NCBI]
|
2.17481e-05
|
|
|
MSD
|
[NCBI]
|
2.10058e-05
|
|
|
LWD
|
[NCBI]
|
2.10058e-05
|
|
|
TBS
|
[NCBI]
|
1.96107e-05
|
|
|
LSA
|
[NCBI]
|
1.89542e-05
|
|
|
hypophosphatemic rickets, x-linked dominant
|
[NCBI]
|
1.89542e-05
|
|
|
CASR
|
[NCBI]
|
1.89044e-05
|
|
|
CSA
|
[NCBI]
|
1.83231e-05
|
|
|
FOP
|
[NCBI]
|
1.83231e-05
|
|
|
sotos syndrome
|
[NCBI]
|
1.77158e-05
|
|
|
CD
|
[NCBI]
|
1.7373e-05
|
|
|
BGLAP
|
[NCBI]
|
1.7071e-05
|
|
|
TRPS2
|
[NCBI]
|
1.54997e-05
|
|
|
RSTS
|
[NCBI]
|
1.54997e-05
|
|
|
PMP22
|
[NCBI]
|
1.53947e-05
|
|
|
RTT
|
[NCBI]
|
1.43288e-05
|
|
|
SRS
|
[NCBI]
|
1.36234e-05
|
|
|
AKR1B1
|
[NCBI]
|
1.32559e-05
|
|
|
SDC2
|
[NCBI]
|
1.19926e-05
|
|
|
CLS
|
[NCBI]
|
1.11288e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
1.07645e-05
|
|
|
TD1
|
[NCBI]
|
1.04112e-05
|
|
|
AHO
|
[NCBI]
|
1.00687e-05
|
|
|
PTH
|
[NCBI]
|
9.85937e-06
|
|
|
mucolipidosis ii
|
[NCBI]
|
9.10128e-06
|
|
|
EV
|
[NCBI]
|
7.66911e-06
|
|
|
CCD
|
[NCBI]
|
6.43124e-06
|
|
|
TNFRSF11B
|
[NCBI]
|
6.36325e-06
|
|
|
VDR
|
[NCBI]
|
5.0021e-06
|
|
|
PWS
|
[NCBI]
|
3.93378e-06
|
|
|
temporal arteritis
|
[NCBI]
|
3.31243e-06
|
|
|
NPPA
|
[NCBI]
|
2.42826e-06
|
|
|
fragile x mental retardation syndrome
|
[NCBI]
|
1.72887e-06
|
|
|
SMS
|
[NCBI]
|
1.16256e-06
|
|
|
MBP
|
[NCBI]
|
1.06821e-06
|
|
|
CHAT
|
[NCBI]
|
1.01103e-06
|
|
|
DFSP
|
[NCBI]
|
9.60685e-07
|
|
|
TNF
|
[NCBI]
|
8.63125e-07
|
|
|
BDNF
|
[NCBI]
|
3.26714e-07
|
|
|
VIP
|
[NCBI]
|
1.58341e-07
|
|
|
AVP
|
[NCBI]
|
1.46727e-07
|
|
|
GFAP
|
[NCBI]
|
5.77428e-08
|
|
|
NPY
|
[NCBI]
|
4.75035e-08
|
|
|
ACHE
|
[NCBI]
|
3.0454e-08
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.95192e-08
|
|
|
VEGF
|
[NCBI]
|
6.33363e-09
|
|
|
TH
|
[NCBI]
|
2.7532e-11
|
|