|
OMIM |
Link |
Information gain |
01 |
|
thrombocytopenia-absent radius syndrome
|
[NCBI]
|
0.0289225
|
|
|
BGS
|
[NCBI]
|
0.00289763
|
|
|
humeroradial synostosis
|
[NCBI]
|
0.00220685
|
|
|
radial heads, posterior dislocation of
|
[NCBI]
|
0.00220685
|
|
|
hemifacial microsomia with radial defects
|
[NCBI]
|
0.00145678
|
|
|
metaphyseal dysplasia, braun-tinschert type
|
[NCBI]
|
0.00110106
|
|
|
ventriculomegaly with defects of the radius and kidney
|
[NCBI]
|
0.00110106
|
|
|
mesomelic dwarfism of hypoplastic tibia and radius type
|
[NCBI]
|
0.00110106
|
|
|
robinow syndrome, autosomal dominant
|
[NCBI]
|
0.000849683
|
|
|
ulnar hypoplasia
|
[NCBI]
|
0.000791708
|
|
|
nievergelt syndrome
|
[NCBI]
|
0.000791708
|
|
|
radioulnar synostosis
|
[NCBI]
|
0.000738026
|
|
|
AFD1
|
[NCBI]
|
0.000693691
|
|
|
mesomelic dysplasia, kantaputra type
|
[NCBI]
|
0.000675971
|
|
|
omodysplasia
|
[NCBI]
|
0.000601389
|
|
|
LWD
|
[NCBI]
|
0.000598661
|
|
|
ABS
|
[NCBI]
|
0.000556081
|
|
|
microcephalic osteodysplastic primordial dwarfism, type i
|
[NCBI]
|
0.000546353
|
|
|
radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation
|
[NCBI]
|
0.000513224
|
|
|
microcephalic osteodysplastic primordial dwarfism, type ii
|
[NCBI]
|
0.000502829
|
|
|
BMND3
|
[NCBI]
|
0.000466912
|
|
|
weyers ulnar ray/oligodactyly syndrome
|
[NCBI]
|
0.000418017
|
|
|
omodysplasia, generalized form
|
[NCBI]
|
0.000409934
|
|
|
kyphomelic dysplasia
|
[NCBI]
|
0.000409934
|
|
|
acroosteolysis with osteoporosis and changes in skull and mandible
|
[NCBI]
|
0.000409934
|
|
|
osteolysis, hereditary, of carpal bones with nephropathy
|
[NCBI]
|
0.000386605
|
|
|
PTH
|
[NCBI]
|
0.000348563
|
|
|
radial aplasia, x-linked
|
[NCBI]
|
0.000341917
|
|
|
humeroradial synostosis
|
[NCBI]
|
0.000341917
|
|
|
radioulnar synostosis with amegakaryocytic thrombocytopenia
|
[NCBI]
|
0.000341917
|
|
|
MLRD
|
[NCBI]
|
0.000246778
|
|
|
vacterl association with hydrocephalus, x-linked
|
[NCBI]
|
0.000233982
|
|
|
RTS
|
[NCBI]
|
0.000227812
|
|
|
MBS
|
[NCBI]
|
0.00021454
|
|
|
paget disease, juvenile
|
[NCBI]
|
0.000189404
|
|
|
DRRS
|
[NCBI]
|
0.00018005
|
|
|
radial ray hypoplasia with choanal atresia
|
[NCBI]
|
0.000170842
|
|
|
metachondromatosis
|
[NCBI]
|
0.000170842
|
|
|
ulnar agenesis and endocardial fibroelastosis
|
[NCBI]
|
0.000170842
|
|
|
lethal short-limb skeletal dysplasia, al gazali type
|
[NCBI]
|
0.000170842
|
|
|
radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema
|
[NCBI]
|
0.000170842
|
|
|
radioulnar synostosis, radial ray abnormalities, and severe malformations in the male
|
[NCBI]
|
0.000170842
|
|
|
ulna and fibula, hypoplasia of
|
[NCBI]
|
0.000170842
|
|
|
pronation-supination of the forearm, impairment of
|
[NCBI]
|
0.000170842
|
|
|
radioulnar synostosis, unilateral, with developmental retardation and hypotonia
|
[NCBI]
|
0.000170842
|
|
|
micromelic dysplasia, congenital, with dislocation of radius
|
[NCBI]
|
0.000131633
|
|
|
phocomelia-ectrodactyly, ear malformation, deafness, and sinus arrhythmia
|
[NCBI]
|
0.000131633
|
|
|
radial-renal syndrome
|
[NCBI]
|
0.000131633
|
|
|
osteopetrosis and infantile neuroaxonal dystrophy
|
[NCBI]
|
0.000131633
|
|
|
renal dysplasia-limb defects syndrome
|
[NCBI]
|
0.000131633
|
|
|
omphalocele, diaphragmatic hernia, and radial ray defects
|
[NCBI]
|
0.000116876
|
|
|
ivic syndrome
|
[NCBI]
|
0.000116876
|
|
|
HOS
|
[NCBI]
|
0.00010834
|
|
|
vacterl association with hydrocephalus
|
[NCBI]
|
0.000107317
|
|
|
corpus callosum, partial agenesis of, x-linked
|
[NCBI]
|
0.000107317
|
|
|
rapadilino syndrome
|
[NCBI]
|
0.000107317
|
|
|
humerospinal dysostosis
|
[NCBI]
|
0.000107317
|
|
|
HOXA11
|
[NCBI]
|
0.000107254
|
|
|
por deficiency
|
[NCBI]
|
9.45889e-05
|
|
|
cleft lip/palate with abnormal thumbs and microcephaly
|
[NCBI]
|
9.45889e-05
|
|
|
AOII
|
[NCBI]
|
9.45889e-05
|
|
|
DBA
|
[NCBI]
|
8.69819e-05
|
|
|
VDR
|
[NCBI]
|
8.22112e-05
|
|
|
vater association
|
[NCBI]
|
7.93498e-05
|
|
|
stuve-wiedemann syndrome
|
[NCBI]
|
7.65798e-05
|
|
|
EDM1
|
[NCBI]
|
7.40685e-05
|
|
|
TWIST1
|
[NCBI]
|
7.14626e-05
|
|
|
SYM1
|
[NCBI]
|
6.96591e-05
|
|
|
camurati-engelmann disease
|
[NCBI]
|
6.77016e-05
|
|
|
sacral defect with anterior meningocele
|
[NCBI]
|
6.41754e-05
|
|
|
radial ray deficiency, x-linked
|
[NCBI]
|
6.04224e-05
|
|
|
EFE
|
[NCBI]
|
5.9645e-05
|
|
|
robinow syndrome, autosomal recessive
|
[NCBI]
|
5.82958e-05
|
|
|
RBS
|
[NCBI]
|
5.24511e-05
|
|
|
PHS
|
[NCBI]
|
4.85943e-05
|
|
|
TBS
|
[NCBI]
|
4.6054e-05
|
|
|
FOP
|
[NCBI]
|
4.44979e-05
|
|
|
SCS
|
[NCBI]
|
4.37563e-05
|
|
|
TRPS2
|
[NCBI]
|
4.10032e-05
|
|
|
CRMO
|
[NCBI]
|
4.10032e-05
|
|
|
NPPB
|
[NCBI]
|
4.09616e-05
|
|
|
FANCB
|
[NCBI]
|
3.97573e-05
|
|
|
RECQL4
|
[NCBI]
|
3.87266e-05
|
|
|
NPS
|
[NCBI]
|
3.85422e-05
|
|
|
plasmin inhibitor deficiency
|
[NCBI]
|
3.70254e-05
|
|
|
SALL4
|
[NCBI]
|
3.56517e-05
|
|
|
SDS
|
[NCBI]
|
3.47906e-05
|
|
|
TD1
|
[NCBI]
|
3.43031e-05
|
|
|
AHO
|
[NCBI]
|
3.38262e-05
|
|
|
CES
|
[NCBI]
|
3.07562e-05
|
|
|
SHOX
|
[NCBI]
|
2.99376e-05
|
|
|
MAS
|
[NCBI]
|
2.84424e-05
|
|
|
L1CAM
|
[NCBI]
|
2.5958e-05
|
|
|
SLC4A1
|
[NCBI]
|
2.4385e-05
|
|
|
BBS
|
[NCBI]
|
2.36209e-05
|
|
|
TNFRSF11B
|
[NCBI]
|
2.31839e-05
|
|
|
FGFR2
|
[NCBI]
|
2.02519e-05
|
|
|
FGFR1
|
[NCBI]
|
1.95146e-05
|
|
|
BGLAP
|
[NCBI]
|
1.79334e-05
|
|
|
IHH
|
[NCBI]
|
1.61323e-05
|
|
|
COMP
|
[NCBI]
|
1.52002e-05
|
|
|
WBS
|
[NCBI]
|
1.17949e-05
|
|
|
FA
|
[NCBI]
|
9.9644e-06
|
|
|
VEGF
|
[NCBI]
|
1.65143e-06
|
|
|
CD
|
[NCBI]
|
3.09995e-07
|
|
|
RA
|
[NCBI]
|
1.65899e-08
|
|
|
TNF
|
[NCBI]
|
2.89213e-10
|
|