|
OMIM |
Link |
Information gain |
01 |
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.0243037
|
|
|
ATS
|
[NCBI]
|
0.0044634
|
|
|
AMMECR1
|
[NCBI]
|
0.00348481
|
|
|
COL4A5
|
[NCBI]
|
0.00213986
|
|
|
renal failure, progressive, with hypertension
|
[NCBI]
|
0.00155147
|
|
|
alport syndrome, autosomal recessive
|
[NCBI]
|
0.00107122
|
|
|
nephropathy, progressive, with deafness
|
[NCBI]
|
0.000864734
|
|
|
leiomyomatosis, esophageal and vulval, with nephropathy
|
[NCBI]
|
0.000820744
|
|
|
FTNS
|
[NCBI]
|
0.000745509
|
|
|
anorectal anomalies
|
[NCBI]
|
0.000647409
|
|
|
COL4A3
|
[NCBI]
|
0.000601317
|
|
|
amme complex
|
[NCBI]
|
0.000508663
|
|
|
epstein syndrome
|
[NCBI]
|
0.00045374
|
|
|
MYH9
|
[NCBI]
|
0.000345071
|
|
|
COL4A6
|
[NCBI]
|
0.000312545
|
|
|
COL4A4
|
[NCBI]
|
0.000257437
|
|
|
SBS
|
[NCBI]
|
0.000240863
|
|
|
BFH
|
[NCBI]
|
0.000231533
|
|
|
nephropathy with pretibial epidermolysis bullosa and deafness
|
[NCBI]
|
0.000229941
|
|
|
IGAN1
|
[NCBI]
|
0.000203624
|
|
|
raph blood group system
|
[NCBI]
|
0.000199
|
|
|
FACL4
|
[NCBI]
|
0.000181549
|
|
|
KCNE1L
|
[NCBI]
|
0.000155918
|
|
|
macrothrombocytopenia and progressive sensorineural deafness
|
[NCBI]
|
0.000114861
|
|
|
MHA
|
[NCBI]
|
0.000113491
|
|
|
MYH10
|
[NCBI]
|
7.78716e-05
|
|
|
goodpasture syndrome
|
[NCBI]
|
7.11054e-05
|
|
|
charcot-marie-tooth disease and deafness
|
[NCBI]
|
7.11054e-05
|
|
|
CD151
|
[NCBI]
|
5.88972e-05
|
|
|
NPHP1
|
[NCBI]
|
4.41795e-05
|
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type i
|
[NCBI]
|
4.3143e-05
|
|
|
complement component 2 deficiency
|
[NCBI]
|
3.50916e-05
|
|
|
polycystic kidneys
|
[NCBI]
|
3.22429e-05
|
|
|
COL7A1
|
[NCBI]
|
3.03731e-05
|
|
|
GUSB
|
[NCBI]
|
2.33908e-05
|
|
|
COL1A1
|
[NCBI]
|
2.25889e-05
|
|
|
GAPDH
|
[NCBI]
|
1.16114e-05
|
|
|
AR
|
[NCBI]
|
4.99617e-07
|
|
|
AFP
|
[NCBI]
|
2.42262e-08
|
|