|
OMIM |
Link |
Information
gain |
01 |
|
|
cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
|
[NCBI]
|
0.000991404
|
|
|
|
oculocerebral syndrome with hypopigmentation
|
[NCBI]
|
0.000817902
|
|
|
|
MCOPS1
|
[NCBI]
|
0.000765046
|
|
|
|
mucopolysaccharidosis type vi
|
[NCBI]
|
0.000136083
|
|
|
|
neurologic disease, infantile multisystem, with osseous fragility
|
[NCBI]
|
0.000129339
|
|
|
|
spastic quadriplegia, retinitis pigmentosa, and mental retardation
|
[NCBI]
|
0.000129339
|
|
|
|
AVP
|
[NCBI]
|
0.000118757
|
|
|
|
SLS
|
[NCBI]
|
0.000107618
|
|
|
|
paine syndrome
|
[NCBI]
|
9.83952e-05
|
|
|
|
schizencephaly
|
[NCBI]
|
9.83952e-05
|
|
|
|
MRAP
|
[NCBI]
|
9.02832e-05
|
|
|
|
branchial myoclonus with spastic paraparesis and cerebellar ataxia
|
[NCBI]
|
8.88018e-05
|
|
|
|
APBD
|
[NCBI]
|
8.05159e-05
|
|
|
|
microcephaly with spastic quadriplegia
|
[NCBI]
|
8.05159e-05
|
|
|
|
LIS1
|
[NCBI]
|
7.84898e-05
|
|
|
|
cerebral palsy, spastic, symmetric, autosomal recessive
|
[NCBI]
|
7.84898e-05
|
|
|
|
ACCPN
|
[NCBI]
|
7.22548e-05
|
|
|
|
3-@methylglutaconic aciduria, type i
|
[NCBI]
|
7.22548e-05
|
|
|
|
AHDS
|
[NCBI]
|
6.68256e-05
|
|
|
|
alexander disease
|
[NCBI]
|
6.50819e-05
|
|
|
|
AGS1
|
[NCBI]
|
6.42765e-05
|
|
|
|
EBN1
|
[NCBI]
|
6.42765e-05
|
|
|
|
AUH
|
[NCBI]
|
6.17519e-05
|
|
|
|
alzheimer disease 3
|
[NCBI]
|
5.89784e-05
|
|
|
|
SLC16A2
|
[NCBI]
|
5.44865e-05
|
|
|
|
KCNQ2
|
[NCBI]
|
5.37769e-05
|
|
|
|
pyruvate decarboxylase deficiency
|
[NCBI]
|
5.22052e-05
|
|
|
|
PAFAH1B1
|
[NCBI]
|
5.03403e-05
|
|
|
|
costello syndrome
|
[NCBI]
|
4.89054e-05
|
|
|
|
CMT1B
|
[NCBI]
|
4.80374e-05
|
|
|
|
PDHA1
|
[NCBI]
|
4.54718e-05
|
|
|
|
AMC
|
[NCBI]
|
4.49809e-05
|
|
|
|
HRAS
|
[NCBI]
|
4.20159e-05
|
|
|
|
RA
|
[NCBI]
|
4.17321e-05
|
|
|
|
FRDA
|
[NCBI]
|
3.66346e-05
|
|
|
|
GUSB
|
[NCBI]
|
3.55467e-05
|
|
|
|
PMD
|
[NCBI]
|
3.4636e-05
|
|
|
|
MBP
|
[NCBI]
|
3.02885e-05
|
|
|
|
NPPA
|
[NCBI]
|
1.39787e-05
|
|
|
|
SLE
|
[NCBI]
|
3.66577e-06
|
|
|
|
TNF
|
[NCBI]
|
2.39873e-07
|
|
