|
OMIM |
Link |
Information gain |
01 |
|
AVP
|
[NCBI]
|
0.00671529
|
|
|
diabetes insipidus, nephrogenic, x-linked
|
[NCBI]
|
0.00216516
|
|
|
diabetes insipidus, neurohypophyseal type
|
[NCBI]
|
0.00191741
|
|
|
WFS1
|
[NCBI]
|
0.00136935
|
|
|
diabetes insipidus, nephrogenic, autosomal
|
[NCBI]
|
0.00107114
|
|
|
AVPR2
|
[NCBI]
|
0.000868917
|
|
|
proteus syndrome
|
[NCBI]
|
0.000830911
|
|
|
AQP2
|
[NCBI]
|
0.000253376
|
|
|
diabetes insipidus, neurohypophyseal type
|
[NCBI]
|
0.000228234
|
|
|
septooptic dysplasia
|
[NCBI]
|
0.000126673
|
|
|
hypopituitarism, congenital, with central diabetes insipidus
|
[NCBI]
|
0.000114013
|
|
|
diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification
|
[NCBI]
|
0.000114013
|
|
|
autonomic control, congenital failure of
|
[NCBI]
|
0.000107379
|
|
|
langerhans cell histiocytosis
|
[NCBI]
|
7.75929e-05
|
|
|
optic nerve hypoplasia, bilateral
|
[NCBI]
|
7.75929e-05
|
|
|
SLE
|
[NCBI]
|
7.74449e-05
|
|
|
pseudopapilledema
|
[NCBI]
|
7.35111e-05
|
|
|
bartter syndrome, antenatal, type 1
|
[NCBI]
|
7.02613e-05
|
|
|
bartter syndrome, antenatal, type 2
|
[NCBI]
|
5.35882e-05
|
|
|
SLSN1
|
[NCBI]
|
4.76449e-05
|
|
|
ALMS
|
[NCBI]
|
4.50489e-05
|
|
|
OXT
|
[NCBI]
|
4.27692e-05
|
|
|
AQP3
|
[NCBI]
|
3.60626e-05
|
|
|
BRRS
|
[NCBI]
|
3.24057e-05
|
|
|
NPPA
|
[NCBI]
|
2.96968e-05
|
|
|
SLC12A3
|
[NCBI]
|
2.69448e-05
|
|
|
AKR1B1
|
[NCBI]
|
2.46713e-05
|
|
|
AQP1
|
[NCBI]
|
1.98829e-05
|
|
|
PTGS2
|
[NCBI]
|
1.41152e-05
|
|
|
AFP
|
[NCBI]
|
1.29357e-05
|
|
|
von willebrand disease
|
[NCBI]
|
8.54823e-06
|
|
|
PRL
|
[NCBI]
|
6.83612e-06
|
|
|
hemophilia a
|
[NCBI]
|
6.36295e-06
|
|
|
CRH
|
[NCBI]
|
5.94763e-06
|
|
|
GNRH1
|
[NCBI]
|
1.75842e-06
|
|
|
PTH
|
[NCBI]
|
6.89432e-07
|
|
|
CCK
|
[NCBI]
|
3.31313e-07
|
|
|
thrombocytopenic purpura, autoimmune
|
[NCBI]
|
4.81837e-08
|
|