|
OMIM |
Link |
Information gain |
01 |
|
MRD
|
[NCBI]
|
0.00134251
|
|
|
van bogaert-hozay syndrome
|
[NCBI]
|
0.00119649
|
|
|
basilar impression, primary
|
[NCBI]
|
0.000931631
|
|
|
spastic diplegia, infantile type
|
[NCBI]
|
0.000931631
|
|
|
SHFM1
|
[NCBI]
|
0.000919553
|
|
|
acanthosis nigricans
|
[NCBI]
|
0.000831882
|
|
|
ophthalmoplegia, familial static
|
[NCBI]
|
0.000831882
|
|
|
CTPP1
|
[NCBI]
|
0.000719246
|
|
|
renal failure, progressive, with hypertension
|
[NCBI]
|
0.000649401
|
|
|
RCD1
|
[NCBI]
|
0.000622333
|
|
|
DFN2
|
[NCBI]
|
0.000622333
|
|
|
TOC
|
[NCBI]
|
0.000577767
|
|
|
telomere length, mean leukocyte
|
[NCBI]
|
0.000541899
|
|
|
alport syndrome, autosomal dominant
|
[NCBI]
|
0.00043447
|
|
|
HSAN2
|
[NCBI]
|
0.000170034
|
|
|
thumb, distal hyperextensibility of
|
[NCBI]
|
0.000145111
|
|
|
OPCA V
|
[NCBI]
|
0.000145111
|
|
|
cervical vertebral bridge
|
[NCBI]
|
0.000145111
|
|
|
polyposis, intestinal, scattered and discrete
|
[NCBI]
|
0.000145111
|
|
|
purpura simplex
|
[NCBI]
|
0.000145111
|
|
|
calcification of joints and arteries
|
[NCBI]
|
0.000145111
|
|
|
hypogonadism, male
|
[NCBI]
|
0.000145111
|
|
|
VMD
|
[NCBI]
|
0.000129127
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
0.000125537
|
|
|
SLS
|
[NCBI]
|
0.000119223
|
|
|
ossified ear cartilages
|
[NCBI]
|
0.000117351
|
|
|
cerebellar ataxia and ectodermal dysplasia
|
[NCBI]
|
0.000117351
|
|
|
toe, misshapen
|
[NCBI]
|
0.000117351
|
|
|
ichthyosis hystrix gravior
|
[NCBI]
|
0.000117351
|
|
|
diabetes insipidus, neurohypophyseal type
|
[NCBI]
|
0.000117351
|
|
|
keloids
|
[NCBI]
|
0.000106882
|
|
|
syndactyly, type iii
|
[NCBI]
|
0.000100089
|
|
|
ectopia lentis
|
[NCBI]
|
0.000100089
|
|
|
CSCD
|
[NCBI]
|
9.50405e-05
|
|
|
enchondromatosis, multiple
|
[NCBI]
|
9.10207e-05
|
|
|
weill-marchesani syndrome, autosomal recessive
|
[NCBI]
|
8.76801e-05
|
|
|
deafness, autosomal recessive
|
[NCBI]
|
8.48224e-05
|
|
|
IHCM
|
[NCBI]
|
8.23257e-05
|
|
|
elliptocytosis, rhesus-unlinked type
|
[NCBI]
|
8.23257e-05
|
|
|
hydrocephalus
|
[NCBI]
|
8.01092e-05
|
|
|
PFHB1A
|
[NCBI]
|
7.81166e-05
|
|
|
OPPG
|
[NCBI]
|
7.46497e-05
|
|
|
diabetes insipidus, nephrogenic, autosomal
|
[NCBI]
|
7.31212e-05
|
|
|
pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities
|
[NCBI]
|
7.31212e-05
|
|
|
MCPH1
|
[NCBI]
|
7.17031e-05
|
|
|
pituitary dwarfism iii
|
[NCBI]
|
6.91419e-05
|
|
|
SCZD1
|
[NCBI]
|
6.91419e-05
|
|
|
pituitary dwarfism i
|
[NCBI]
|
6.79769e-05
|
|
|
EL1
|
[NCBI]
|
6.58368e-05
|
|
|
donohue syndrome
|
[NCBI]
|
6.39086e-05
|
|
|
CHNG2
|
[NCBI]
|
6.30118e-05
|
|
|
OCRL
|
[NCBI]
|
6.13339e-05
|
|
|
RCDP1
|
[NCBI]
|
5.97899e-05
|
|
|
cystinuria
|
[NCBI]
|
5.63977e-05
|
|
|
IGER
|
[NCBI]
|
5.14902e-05
|
|
|
NPS
|
[NCBI]
|
4.88075e-05
|
|
|
hypertrophic neuropathy of dejerine-sottas
|
[NCBI]
|
4.83954e-05
|
|
|
maple syrup urine disease
|
[NCBI]
|
4.75975e-05
|
|
|
CHM
|
[NCBI]
|
4.60974e-05
|
|
|
TCOF
|
[NCBI]
|
4.43784e-05
|
|
|
tritanopia
|
[NCBI]
|
4.21584e-05
|
|
|
ALS1
|
[NCBI]
|
4.16392e-05
|
|
|
WT1
|
[NCBI]
|
3.58854e-05
|
|
|
OA1
|
[NCBI]
|
3.5289e-05
|
|
|
coproporphyria
|
[NCBI]
|
3.51284e-05
|
|
|
giant platelet syndrome
|
[NCBI]
|
3.48905e-05
|
|
|
SCZD
|
[NCBI]
|
3.41337e-05
|
|
|
KIT
|
[NCBI]
|
3.26924e-05
|
|
|
EV
|
[NCBI]
|
3.23754e-05
|
|
|
factor v deficiency
|
[NCBI]
|
3.03725e-05
|
|
|
INSR
|
[NCBI]
|
2.7413e-05
|
|
|
adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency
|
[NCBI]
|
2.52674e-05
|
|
|
TS
|
[NCBI]
|
1.00839e-05
|
|