|
OMIM |
Link |
Information
gain |
01 |
|
|
hereditary motor and sensory neuropathy v
|
[NCBI]
|
0.00235899
|
|
|
|
ketoaciduria with mental deficiency and other features
|
[NCBI]
|
0.00158502
|
|
|
|
neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive
|
[NCBI]
|
0.0012742
|
|
|
|
auditory neuropathy, autosomal dominant, 1
|
[NCBI]
|
0.00115699
|
|
|
|
SCAX1
|
[NCBI]
|
0.000979436
|
|
|
|
HNPP
|
[NCBI]
|
0.000455972
|
|
|
|
median-ulnar nerve communications
|
[NCBI]
|
0.000419559
|
|
|
|
SPG3A
|
[NCBI]
|
0.000241926
|
|
|
|
posterior column ataxia
|
[NCBI]
|
0.000209323
|
|
|
|
MG
|
[NCBI]
|
0.000201141
|
|
|
|
slowed nerve conduction velocity, autosomal dominant
|
[NCBI]
|
0.000170063
|
|
|
|
spinocerebellar ataxia, x-linked 3
|
[NCBI]
|
0.000170063
|
|
|
|
charcot-marie-tooth disease, dominant intermediate b
|
[NCBI]
|
0.000138503
|
|
|
|
schwannomatosis
|
[NCBI]
|
0.000132816
|
|
|
|
charcot-marie-tooth disease, axonal, type 2j
|
[NCBI]
|
0.000132816
|
|
|
|
ALS4
|
[NCBI]
|
0.000132816
|
|
|
|
MPZ
|
[NCBI]
|
0.00013009
|
|
|
|
lipomatosis, familial benign cervical
|
[NCBI]
|
0.000124045
|
|
|
|
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 1
|
[NCBI]
|
0.000114553
|
|
|
|
HOKPP
|
[NCBI]
|
0.00010748
|
|
|
|
sacral defect with anterior meningocele
|
[NCBI]
|
0.000101844
|
|
|
|
refsum disease
|
[NCBI]
|
0.000100194
|
|
|
|
cerebrotendinous xanthomatosis
|
[NCBI]
|
8.65634e-05
|
|
|
|
CMTX1
|
[NCBI]
|
8.46761e-05
|
|
|
|
CMT1B
|
[NCBI]
|
7.7505e-05
|
|
|
|
PMP22
|
[NCBI]
|
6.53728e-05
|
|
|
|
KSS
|
[NCBI]
|
5.00679e-05
|
|
|
|
dystrophia myotonica 1
|
[NCBI]
|
4.46255e-05
|
|
|
|
CLCN1
|
[NCBI]
|
4.14771e-05
|
|
|
|
NF2
|
[NCBI]
|
3.86098e-05
|
|
|
|
SMN1
|
[NCBI]
|
3.52197e-05
|
|
|
|
MUC1
|
[NCBI]
|
2.0772e-05
|
|
|
|
ACHE
|
[NCBI]
|
6.85757e-06
|
|
|
|
NGFB
|
[NCBI]
|
3.89028e-06
|
|
|
|
SLE
|
[NCBI]
|
3.86799e-06
|
|
