|
OMIM |
Link |
Information gain |
01 |
|
pseudohyperkalemia, familial, 1, due to red cell leak
|
[NCBI]
|
0.00365165
|
|
|
DHS
|
[NCBI]
|
0.0030169
|
|
|
HYPP
|
[NCBI]
|
0.00211937
|
|
|
PHA2
|
[NCBI]
|
0.00173247
|
|
|
malignant hyperthermia, susceptibility to, 2
|
[NCBI]
|
0.000724991
|
|
|
WNK4
|
[NCBI]
|
0.000543414
|
|
|
stomatocytosis i
|
[NCBI]
|
0.0005041
|
|
|
corticosterone methyloxidase type ii deficiency
|
[NCBI]
|
0.000343582
|
|
|
PMC
|
[NCBI]
|
0.000295262
|
|
|
SCN4A
|
[NCBI]
|
0.000293468
|
|
|
WNK1
|
[NCBI]
|
0.000286649
|
|
|
dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema
|
[NCBI]
|
0.000188242
|
|
|
bartter syndrome, antenatal, type 2
|
[NCBI]
|
0.000135609
|
|
|
RA
|
[NCBI]
|
0.000131741
|
|
|
corticosterone methyloxidase type i deficiency
|
[NCBI]
|
0.000116461
|
|
|
CYP11B2
|
[NCBI]
|
0.00011117
|
|
|
normokalemic periodic paralysis
|
[NCBI]
|
9.40003e-05
|
|
|
GRA
|
[NCBI]
|
9.01434e-05
|
|
|
pseudohyperkalemia cardiff
|
[NCBI]
|
8.00342e-05
|
|
|
carnitine palmitoyltransferase ii deficiency, lethal neonatal
|
[NCBI]
|
6.76849e-05
|
|
|
bartter syndrome, infantile, with sensorineural deafness
|
[NCBI]
|
6.56654e-05
|
|
|
myotonia, potassium-aggravated
|
[NCBI]
|
6.56654e-05
|
|
|
PHA1
|
[NCBI]
|
5.50038e-05
|
|
|
SLOS
|
[NCBI]
|
5.0984e-05
|
|
|
HOKPP
|
[NCBI]
|
4.74441e-05
|
|
|
hyperglycerolemia
|
[NCBI]
|
4.68558e-05
|
|
|
andersen cardiodysrhythmic periodic paralysis
|
[NCBI]
|
4.62889e-05
|
|
|
bartter syndrome, type 3
|
[NCBI]
|
4.4703e-05
|
|
|
CF
|
[NCBI]
|
3.88316e-05
|
|
|
SLE
|
[NCBI]
|
3.87134e-05
|
|
|
NPPA
|
[NCBI]
|
3.62382e-05
|
|
|
hypertension, essential
|
[NCBI]
|
3.34878e-05
|
|
|
IL6
|
[NCBI]
|
2.99321e-05
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
2.53047e-05
|
|
|
CFTR
|
[NCBI]
|
9.64886e-06
|
|
|
EPO
|
[NCBI]
|
4.21476e-06
|
|
|
FMF
|
[NCBI]
|
3.49401e-06
|
|
|
PTH
|
[NCBI]
|
1.25147e-06
|
|