|
OMIM |
Link |
Information gain |
01 |
|
megaduodenum and/or megacystis
|
[NCBI]
|
0.00600518
|
|
|
visceral myopathy, familial, with external ophthalmoplegia
|
[NCBI]
|
0.00441496
|
|
|
visceral neuropathy, familial, autosomal recessive
|
[NCBI]
|
0.00198068
|
|
|
MGS
|
[NCBI]
|
0.00191188
|
|
|
visceral neuropathy, familial, autosomal dominant
|
[NCBI]
|
0.00147665
|
|
|
MNGIE
|
[NCBI]
|
0.000590684
|
|
|
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked
|
[NCBI]
|
0.000440442
|
|
|
achalasia, familial esophageal
|
[NCBI]
|
0.000379617
|
|
|
SPS
|
[NCBI]
|
0.000199197
|
|
|
SLE
|
[NCBI]
|
0.000142588
|
|
|
SOX10
|
[NCBI]
|
0.000116063
|
|
|
FLNA
|
[NCBI]
|
0.000108008
|
|
|
L1CAM
|
[NCBI]
|
0.000107464
|
|
|
PCWH
|
[NCBI]
|
9.51693e-05
|
|
|
myopathy, myofibrillar, desmin-related
|
[NCBI]
|
6.24072e-05
|
|
|
ECGF1
|
[NCBI]
|
5.89764e-05
|
|
|
MYH11
|
[NCBI]
|
4.94173e-05
|
|
|
DES
|
[NCBI]
|
4.68859e-05
|
|
|
VIP
|
[NCBI]
|
4.37089e-05
|
|
|
tyrosinemia, type i
|
[NCBI]
|
4.06738e-05
|
|
|
HSCR1
|
[NCBI]
|
3.63557e-05
|
|
|
RA
|
[NCBI]
|
3.28911e-05
|
|
|
CP
|
[NCBI]
|
2.872e-05
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
2.80488e-05
|
|
|
PCNA
|
[NCBI]
|
6.40197e-06
|
|
|
MG
|
[NCBI]
|
3.7199e-06
|
|