|
OMIM |
Link |
Information gain |
01 |
|
ALD
|
[NCBI]
|
0.0077843
|
|
|
pelizaeus-merzbacher-like disease, autosomal recessive, 2
|
[NCBI]
|
0.00537675
|
|
|
PMD
|
[NCBI]
|
0.00446552
|
|
|
PLP1
|
[NCBI]
|
0.00187476
|
|
|
alpers diffuse degeneration of cerebral gray matter with hepatic cirrhosis
|
[NCBI]
|
0.00107682
|
|
|
metachromatic leukodystrophy
|
[NCBI]
|
0.00102996
|
|
|
ASD1
|
[NCBI]
|
0.000689681
|
|
|
progeroid syndrome, neonatal
|
[NCBI]
|
0.000587372
|
|
|
SLE
|
[NCBI]
|
0.000486939
|
|
|
krabbe disease
|
[NCBI]
|
0.000442233
|
|
|
adrenoleukodystrophy, autosomal neonatal form
|
[NCBI]
|
0.000326261
|
|
|
POLG
|
[NCBI]
|
0.000315544
|
|
|
ABCD1
|
[NCBI]
|
0.00028315
|
|
|
canavan disease
|
[NCBI]
|
0.000268864
|
|
|
SPG2
|
[NCBI]
|
0.000211502
|
|
|
leukodystrophy, adult-onset, autosomal dominant
|
[NCBI]
|
0.000196683
|
|
|
alexander disease
|
[NCBI]
|
0.000146015
|
|
|
refsum disease, infantile form
|
[NCBI]
|
0.000130725
|
|
|
MSD
|
[NCBI]
|
0.000119259
|
|
|
CADASIL
|
[NCBI]
|
0.000113805
|
|
|
ZS
|
[NCBI]
|
9.77748e-05
|
|
|
cerebral sclerosis similar to pelizaeus-merzbacher disease
|
[NCBI]
|
9.4018e-05
|
|
|
megalencephaly with dysmyelination
|
[NCBI]
|
9.4018e-05
|
|
|
VWM
|
[NCBI]
|
7.49699e-05
|
|
|
ABAT
|
[NCBI]
|
6.59934e-05
|
|
|
FEB3
|
[NCBI]
|
6.31613e-05
|
|
|
MTTF
|
[NCBI]
|
5.12523e-05
|
|
|
peroxisomal acyl-coa oxidase deficiency
|
[NCBI]
|
5.04402e-05
|
|
|
PXMP3
|
[NCBI]
|
4.74843e-05
|
|
|
ACOX1
|
[NCBI]
|
4.55901e-05
|
|
|
microcephaly with spastic quadriplegia
|
[NCBI]
|
4.55002e-05
|
|
|
EIF2B5
|
[NCBI]
|
4.4764e-05
|
|
|
CRYAB
|
[NCBI]
|
3.98704e-05
|
|
|
d-bifunctional protein deficiency
|
[NCBI]
|
3.51481e-05
|
|
|
PSAP
|
[NCBI]
|
3.41866e-05
|
|
|
INAD1
|
[NCBI]
|
3.22459e-05
|
|
|
NBIA1
|
[NCBI]
|
2.84165e-05
|
|
|
AHC
|
[NCBI]
|
2.34032e-05
|
|
|
niemann-pick disease, type a
|
[NCBI]
|
2.34032e-05
|
|
|
MAG
|
[NCBI]
|
1.75973e-05
|
|
|
CSA
|
[NCBI]
|
1.6153e-05
|
|
|
neuraminidase deficiency
|
[NCBI]
|
1.6153e-05
|
|
|
mucolipidosis ii
|
[NCBI]
|
1.53995e-05
|
|
|
CMT1A
|
[NCBI]
|
1.26262e-05
|
|
|
MBP
|
[NCBI]
|
1.22256e-05
|
|
|
gaucher disease, type i
|
[NCBI]
|
1.09084e-05
|
|
|
fabry disease
|
[NCBI]
|
6.19763e-06
|
|
|
TSD
|
[NCBI]
|
1.9702e-06
|
|
|
GFAP
|
[NCBI]
|
4.97059e-07
|
|
|
panencephalitis, subacute sclerosing
|
[NCBI]
|
4.85292e-08
|
|