|
OMIM |
Link |
Information gain |
01 |
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
0.00565996
|
|
|
OPMD
|
[NCBI]
|
0.00212214
|
|
|
megaduodenum and/or megacystis
|
[NCBI]
|
0.000907667
|
|
|
TARPS
|
[NCBI]
|
0.000714117
|
|
|
adducted thumbs syndrome
|
[NCBI]
|
0.000632262
|
|
|
indifference to pain, congenital, autosomal dominant
|
[NCBI]
|
0.000579249
|
|
|
laryngeal abductor paralysis
|
[NCBI]
|
0.000539935
|
|
|
gastroesophageal reflux
|
[NCBI]
|
0.000349722
|
|
|
scleroderma, familial progressive
|
[NCBI]
|
0.000287577
|
|
|
MAFD6
|
[NCBI]
|
0.000254299
|
|
|
MG
|
[NCBI]
|
0.000245958
|
|
|
SPS
|
[NCBI]
|
0.000181189
|
|
|
RA
|
[NCBI]
|
0.00017798
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000127275
|
|
|
insensitivity to pain with hyperplastic myelinopathy
|
[NCBI]
|
0.000112629
|
|
|
esophageal ring, lower
|
[NCBI]
|
0.000112629
|
|
|
KSS
|
[NCBI]
|
0.000101367
|
|
|
CHAC
|
[NCBI]
|
9.98575e-05
|
|
|
FSHMD1A
|
[NCBI]
|
9.69594e-05
|
|
|
ophthalmoplegic neuromuscular disorder with abnormal mitochondria
|
[NCBI]
|
9.01715e-05
|
|
|
odontoma-dysphagia syndrome
|
[NCBI]
|
9.01715e-05
|
|
|
SLE
|
[NCBI]
|
8.92081e-05
|
|
|
UCHL3
|
[NCBI]
|
8.42364e-05
|
|
|
RSTS
|
[NCBI]
|
8.31402e-05
|
|
|
dysphasia, familial developmental
|
[NCBI]
|
8.17048e-05
|
|
|
thalamic degeneration, symmetric infantile
|
[NCBI]
|
8.17048e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
8.15717e-05
|
|
|
AMC
|
[NCBI]
|
7.97251e-05
|
|
|
pierre robin syndrome
|
[NCBI]
|
7.6212e-05
|
|
|
MID1
|
[NCBI]
|
7.32571e-05
|
|
|
cleft larynx, posterior
|
[NCBI]
|
6.88829e-05
|
|
|
dystonia, familial, with visual failure and striatal lucencies
|
[NCBI]
|
6.88829e-05
|
|
|
UCHL1
|
[NCBI]
|
6.81758e-05
|
|
|
ATXN2
|
[NCBI]
|
6.74106e-05
|
|
|
SRS
|
[NCBI]
|
6.73532e-05
|
|
|
opitz syndrome
|
[NCBI]
|
6.00702e-05
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive
|
[NCBI]
|
5.56647e-05
|
|
|
SNDI
|
[NCBI]
|
5.56647e-05
|
|
|
SPCH1
|
[NCBI]
|
4.70099e-05
|
|
|
HNA
|
[NCBI]
|
4.55988e-05
|
|
|
PSNP1
|
[NCBI]
|
4.43055e-05
|
|
|
alzheimer disease 3
|
[NCBI]
|
4.25488e-05
|
|
|
EBR1
|
[NCBI]
|
4.20052e-05
|
|
|
MSS
|
[NCBI]
|
4.09727e-05
|
|
|
CP
|
[NCBI]
|
3.9521e-05
|
|
|
MJD
|
[NCBI]
|
3.9186e-05
|
|
|
HP
|
[NCBI]
|
3.6226e-05
|
|
|
SJS1
|
[NCBI]
|
3.52282e-05
|
|
|
HSAN3
|
[NCBI]
|
3.45619e-05
|
|
|
GIST
|
[NCBI]
|
3.38093e-05
|
|
|
CTNS
|
[NCBI]
|
3.27265e-05
|
|
|
HNPP
|
[NCBI]
|
3.24418e-05
|
|
|
SCA7
|
[NCBI]
|
3.18886e-05
|
|
|
SCA2
|
[NCBI]
|
2.68985e-05
|
|
|
apnea, obstructive sleep
|
[NCBI]
|
2.52912e-05
|
|
|
SCA1
|
[NCBI]
|
2.33812e-05
|
|
|
SMAX1
|
[NCBI]
|
1.79344e-05
|
|
|
PCNA
|
[NCBI]
|
1.57012e-05
|
|
|
PD
|
[NCBI]
|
9.93787e-06
|
|
|
AD
|
[NCBI]
|
7.78472e-06
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
1.78152e-06
|
|
|
PWS
|
[NCBI]
|
1.24469e-06
|
|