|
OMIM |
Link |
Information
gain |
01 |
|
|
muscle cramps, familial
|
[NCBI]
|
0.00243653
|
|
|
|
S CRAMP
|
[NCBI]
|
0.00119841
|
|
|
|
FTSD
|
[NCBI]
|
0.00098052
|
|
|
|
DYT7
|
[NCBI]
|
0.000805308
|
|
|
|
glycogen storage disease v
|
[NCBI]
|
0.000237787
|
|
|
|
AMPD1
|
[NCBI]
|
0.000214034
|
|
|
|
muscle glycogenosis, x-linked
|
[NCBI]
|
0.000207385
|
|
|
|
BMD
|
[NCBI]
|
0.000135376
|
|
|
|
acanthosis nigricans with muscle cramps and acral enlargement
|
[NCBI]
|
0.000134271
|
|
|
|
cramps, familial adolescent
|
[NCBI]
|
0.000134271
|
|
|
|
SMAX1
|
[NCBI]
|
9.85305e-05
|
|
|
|
HANAC
|
[NCBI]
|
9.782e-05
|
|
|
|
phosphorylase kinase deficiency of liver and muscle, autosomal recessive
|
[NCBI]
|
9.04679e-05
|
|
|
|
spinal muscular atrophy, proximal, adult, autosomal dominant
|
[NCBI]
|
8.34102e-05
|
|
|
|
myotonia, potassium-aggravated
|
[NCBI]
|
8.34102e-05
|
|
|
|
DMD
|
[NCBI]
|
8.22363e-05
|
|
|
|
brody myopathy
|
[NCBI]
|
8.16093e-05
|
|
|
|
HOMG3
|
[NCBI]
|
7.59252e-05
|
|
|
|
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis
|
[NCBI]
|
7.2683e-05
|
|
|
|
myotonia congenita, autosomal dominant
|
[NCBI]
|
6.91794e-05
|
|
|
|
PHKA1
|
[NCBI]
|
6.724e-05
|
|
|
|
carnitine palmitoyltransferase ii deficiency, late-onset
|
[NCBI]
|
6.6977e-05
|
|
|
|
RMD
|
[NCBI]
|
6.63054e-05
|
|
|
|
COL4A1
|
[NCBI]
|
6.45705e-05
|
|
|
|
lactase persistence
|
[NCBI]
|
6.22591e-05
|
|
|
|
PYGM
|
[NCBI]
|
5.58217e-05
|
|
|
|
DYT1
|
[NCBI]
|
5.40621e-05
|
|
|
|
SCN4A
|
[NCBI]
|
4.93128e-05
|
|
|
|
DMD
|
[NCBI]
|
3.41339e-05
|
|
|
|
RA
|
[NCBI]
|
2.44243e-05
|
|
|
|
PTH
|
[NCBI]
|
6.16509e-06
|
|
