|
OMIM |
Link |
Information
gain |
01 |
|
|
apnea, obstructive sleep
|
[NCBI]
|
0.000835316
|
|
|
|
VUR1
|
[NCBI]
|
0.000710915
|
|
|
|
CF
|
[NCBI]
|
0.000268936
|
|
|
|
amyotonia congenita
|
[NCBI]
|
0.000152565
|
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
0.000113753
|
|
|
|
rheumatoid arthritis, systemic juvenile
|
[NCBI]
|
9.22454e-05
|
|
|
|
mucopolysaccharidosis type iva
|
[NCBI]
|
8.00602e-05
|
|
|
|
EBN1
|
[NCBI]
|
7.42516e-05
|
|
|
|
glycogen storage disease iii
|
[NCBI]
|
7.03681e-05
|
|
|
|
thrombasthenia of glanzmann and naegeli
|
[NCBI]
|
4.61245e-05
|
|
|
|
CDLS1
|
[NCBI]
|
4.2726e-05
|
|
|
|
KCNQ2
|
[NCBI]
|
4.13781e-05
|
|
|
|
CJD
|
[NCBI]
|
3.27593e-05
|
|
|
|
HPRT1
|
[NCBI]
|
2.90912e-05
|
|
|
|
SLE
|
[NCBI]
|
2.84457e-05
|
|
|
|
MODY
|
[NCBI]
|
2.69822e-05
|
|
|
|
GJB2
|
[NCBI]
|
2.64416e-05
|
|
|
|
MFS
|
[NCBI]
|
2.64101e-05
|
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
2.62588e-05
|
|
|
|
RTT
|
[NCBI]
|
2.49541e-05
|
|
|
|
GTS
|
[NCBI]
|
2.05391e-05
|
|
|
|
FA
|
[NCBI]
|
1.11585e-05
|
|
