|
OMIM |
Link |
Information gain |
01 |
|
megaduodenum and/or megacystis
|
[NCBI]
|
0.00970204
|
|
|
volvulus of midgut
|
[NCBI]
|
0.00274066
|
|
|
visceral neuropathy, familial, autosomal recessive
|
[NCBI]
|
0.00269606
|
|
|
CF
|
[NCBI]
|
0.00187867
|
|
|
jejunal atresia
|
[NCBI]
|
0.00173084
|
|
|
CFM1
|
[NCBI]
|
0.00152161
|
|
|
visceral myopathy, familial, with external ophthalmoplegia
|
[NCBI]
|
0.00122277
|
|
|
intestinal atresia, multiple
|
[NCBI]
|
0.000948967
|
|
|
visceral neuropathy, familial, autosomal dominant
|
[NCBI]
|
0.000555675
|
|
|
basal ganglia calcification, idiopathic, childhood-onset
|
[NCBI]
|
0.000385833
|
|
|
megacystis-microcolon-intestinal hypoperistalsis syndrome
|
[NCBI]
|
0.00034774
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.000155525
|
|
|
HSCR1
|
[NCBI]
|
0.000144921
|
|
|
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked
|
[NCBI]
|
0.000144576
|
|
|
CFTR
|
[NCBI]
|
0.00013212
|
|
|
SLE
|
[NCBI]
|
0.000131039
|
|
|
intestinal pseudoobstruction with patent ductus arteriosus and natal teeth
|
[NCBI]
|
0.000108618
|
|
|
duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery
|
[NCBI]
|
0.000108618
|
|
|
VIP
|
[NCBI]
|
0.0001079
|
|
|
GUCY1B3
|
[NCBI]
|
8.26658e-05
|
|
|
splenogonadal fusion with limb defects and micrognathia
|
[NCBI]
|
6.81384e-05
|
|
|
jejunal atresia with microcephaly and ocular anomalies
|
[NCBI]
|
6.81384e-05
|
|
|
CRC
|
[NCBI]
|
6.75974e-05
|
|
|
CGD
|
[NCBI]
|
6.61609e-05
|
|
|
pelvis-shoulder dysplasia
|
[NCBI]
|
6.48942e-05
|
|
|
pancreas, annular
|
[NCBI]
|
6.21996e-05
|
|
|
SLC1A5
|
[NCBI]
|
6.03129e-05
|
|
|
FMF
|
[NCBI]
|
5.48884e-05
|
|
|
waardenburg-shah syndrome
|
[NCBI]
|
4.63494e-05
|
|
|
DMD
|
[NCBI]
|
4.18117e-05
|
|
|
XDH
|
[NCBI]
|
4.09516e-05
|
|
|
epidermolysis bullosa with pyloric atresia
|
[NCBI]
|
3.98005e-05
|
|
|
RP3
|
[NCBI]
|
3.76008e-05
|
|
|
DES
|
[NCBI]
|
3.73256e-05
|
|
|
autonomic control, congenital failure of
|
[NCBI]
|
3.70977e-05
|
|
|
PJS
|
[NCBI]
|
3.70124e-05
|
|
|
SGBS1
|
[NCBI]
|
3.61395e-05
|
|
|
wolman disease
|
[NCBI]
|
3.53245e-05
|
|
|
RP2
|
[NCBI]
|
3.44596e-05
|
|
|
FDH
|
[NCBI]
|
3.17549e-05
|
|
|
GIST
|
[NCBI]
|
2.71226e-05
|
|
|
WS1
|
[NCBI]
|
2.70937e-05
|
|
|
MPO
|
[NCBI]
|
2.66298e-05
|
|
|
GAL
|
[NCBI]
|
2.60442e-05
|
|
|
ABP1
|
[NCBI]
|
2.59586e-05
|
|
|
DMD
|
[NCBI]
|
2.0946e-05
|
|
|
ACHE
|
[NCBI]
|
2.01843e-05
|
|
|
CRH
|
[NCBI]
|
1.82405e-05
|
|
|
NF1
|
[NCBI]
|
1.59946e-05
|
|
|
GDNF
|
[NCBI]
|
1.18641e-05
|
|
|
CCK
|
[NCBI]
|
5.83255e-06
|
|
|
CEACAM5
|
[NCBI]
|
3.91761e-06
|
|
|
AVP
|
[NCBI]
|
2.71913e-06
|
|
|
VEGF
|
[NCBI]
|
2.70024e-06
|
|
|
temporal arteritis
|
[NCBI]
|
2.10092e-06
|
|
|
APC
|
[NCBI]
|
1.60656e-06
|
|
|
TNF
|
[NCBI]
|
2.69112e-07
|
|