|
OMIM |
Link |
Information gain |
01 |
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.00708016
|
|
|
renal failure, progressive, with hypertension
|
[NCBI]
|
0.00452734
|
|
|
IGAN1
|
[NCBI]
|
0.00278078
|
|
|
BFH
|
[NCBI]
|
0.00106474
|
|
|
klippel-trenaunay-weber syndrome
|
[NCBI]
|
0.000922599
|
|
|
ATS
|
[NCBI]
|
0.000253024
|
|
|
alport syndrome, autosomal recessive
|
[NCBI]
|
0.000241564
|
|
|
HANAC
|
[NCBI]
|
0.000188729
|
|
|
COL4A4
|
[NCBI]
|
0.000128409
|
|
|
cryofibrinogenemia, familial primary
|
[NCBI]
|
0.000116703
|
|
|
thrombocytopenia with elevated serum iga and renal disease
|
[NCBI]
|
0.000116703
|
|
|
polycystic kidneys
|
[NCBI]
|
0.000112204
|
|
|
SLE
|
[NCBI]
|
0.000104541
|
|
|
COL4A3
|
[NCBI]
|
0.000100817
|
|
|
beeturia
|
[NCBI]
|
9.42421e-05
|
|
|
hypervitaminosis a, susceptibility to
|
[NCBI]
|
9.42421e-05
|
|
|
deafness, cochlear, with myopia and intellectual impairment
|
[NCBI]
|
9.42421e-05
|
|
|
factor viii deficiency
|
[NCBI]
|
8.57719e-05
|
|
|
coloboma, uveal, with cleft lip and palate and mental retardation
|
[NCBI]
|
8.57719e-05
|
|
|
fibrosclerosis, multifocal
|
[NCBI]
|
8.02756e-05
|
|
|
membranoproliferative glomerulonephritis, x-linked
|
[NCBI]
|
7.61917e-05
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
7.29396e-05
|
|
|
donnai-barrow syndrome
|
[NCBI]
|
7.02373e-05
|
|
|
hyperprolinemia, type i
|
[NCBI]
|
5.96972e-05
|
|
|
COL4A1
|
[NCBI]
|
5.51571e-05
|
|
|
methylmalonic aciduria and homocystinuria, cblc type
|
[NCBI]
|
5.02861e-05
|
|
|
NPHS1
|
[NCBI]
|
4.95931e-05
|
|
|
COL4A5
|
[NCBI]
|
4.21681e-05
|
|
|
C3
|
[NCBI]
|
4.12686e-05
|
|
|
HBB
|
[NCBI]
|
4.0503e-05
|
|
|
UGB
|
[NCBI]
|
3.8979e-05
|
|
|
factor x deficiency
|
[NCBI]
|
3.8979e-05
|
|
|
HAE
|
[NCBI]
|
3.4966e-05
|
|
|
FGA
|
[NCBI]
|
3.46508e-05
|
|
|
RNASE3
|
[NCBI]
|
3.41471e-05
|
|
|
HPRT1
|
[NCBI]
|
3.04608e-05
|
|
|
wilson disease
|
[NCBI]
|
2.55448e-05
|
|
|
CEACAM5
|
[NCBI]
|
2.16934e-05
|
|
|
KLK3
|
[NCBI]
|
2.14857e-05
|
|
|
PCNA
|
[NCBI]
|
1.46025e-05
|
|
|
WAS
|
[NCBI]
|
1.14102e-05
|
|
|
temporal arteritis
|
[NCBI]
|
6.53826e-06
|
|
|
AR
|
[NCBI]
|
4.89922e-06
|
|
|
FMF
|
[NCBI]
|
3.62109e-06
|
|
|
RA
|
[NCBI]
|
2.30465e-06
|
|
|
PTH
|
[NCBI]
|
7.55162e-07
|
|
|
VEGF
|
[NCBI]
|
4.4709e-07
|
|
|
TNF
|
[NCBI]
|
1.47454e-07
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
6.35105e-08
|
|