|
OMIM |
Link |
Information gain |
01 |
|
glycogen storage disease v
|
[NCBI]
|
0.00276097
|
|
|
WDM
|
[NCBI]
|
0.00240735
|
|
|
PYGM
|
[NCBI]
|
0.000741193
|
|
|
phosphorylase kinase deficiency of liver and muscle, autosomal recessive
|
[NCBI]
|
0.000591989
|
|
|
glycogen storage disease vi
|
[NCBI]
|
0.000248792
|
|
|
glycogen storage disease iii
|
[NCBI]
|
0.000186671
|
|
|
PYGB
|
[NCBI]
|
0.000139197
|
|
|
glycogen storage disease of heart, lethal congenital
|
[NCBI]
|
0.000122832
|
|
|
muscle glycogenosis, x-linked
|
[NCBI]
|
0.000112507
|
|
|
tibial muscular dystrophy, tardive
|
[NCBI]
|
0.000105446
|
|
|
central core disease of muscle
|
[NCBI]
|
7.95779e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
7.6872e-05
|
|
|
phosphoglycerate mutase, muscle, deficiency of
|
[NCBI]
|
6.47619e-05
|
|
|
MHS1
|
[NCBI]
|
6.07421e-05
|
|
|
OPMD
|
[NCBI]
|
5.41318e-05
|
|
|
KSS
|
[NCBI]
|
4.41005e-05
|
|
|
RASGRP2
|
[NCBI]
|
3.88617e-05
|
|
|
FAU
|
[NCBI]
|
3.60607e-05
|
|
|
SSTR4
|
[NCBI]
|
3.4242e-05
|
|
|
GAPDH
|
[NCBI]
|
3.2248e-05
|
|
|
ROM1
|
[NCBI]
|
3.09169e-05
|
|
|
PGAM1
|
[NCBI]
|
3.01502e-05
|
|
|
PHKB
|
[NCBI]
|
3.01502e-05
|
|
|
THBD
|
[NCBI]
|
2.62673e-05
|
|
|
glycogen storage disease ixa
|
[NCBI]
|
2.1556e-05
|
|
|
CHGA
|
[NCBI]
|
2.1416e-05
|
|
|
MEN1
|
[NCBI]
|
1.68876e-05
|
|
|
G6PD
|
[NCBI]
|
1.36004e-05
|
|
|
ACHE
|
[NCBI]
|
9.85902e-06
|
|
|
GHRH
|
[NCBI]
|
7.94977e-06
|
|
|
GFAP
|
[NCBI]
|
5.13588e-06
|
|
|
EGF
|
[NCBI]
|
1.70292e-06
|
|
|
TNF
|
[NCBI]
|
1.64645e-06
|
|
|
LPL
|
[NCBI]
|
1.59434e-06
|
|
|
VIP
|
[NCBI]
|
5.46975e-07
|
|
|
PCNA
|
[NCBI]
|
3.85839e-07
|
|