Search results for egr2

Showing 25 of 406 hits for egr2
# Family MCID Name MIFTS Score
1
CHR629 Charcot-Marie-Tooth Disease and Deafness 58 48.319
2
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 66 42.279
3
c CHR653 Charcot-Marie-Tooth Disease, Demyelinating, Type 1d 41 41.715
4
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 54 38.564
5
P CHR071 Charcot-Marie-Tooth Disease 64 29.290
6
P NRP001 Neuropathy 58 18.394
7
TTH006 Tooth Disease 47 17.699
8
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 67 13.279
9
P PLY019 Polyneuropathy 53 11.567
10
P SCL018 Scoliosis 56 11.554
11
SNS003 Sensory Peripheral Neuropathy 51 10.890
12
P RTT002 Rett Syndrome 78 10.844
13
P PRP019 Peripheral Nervous System Disease 63 9.474
14
P DMY001 Demyelinating Polyneuropathy 46 8.525
15
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 58 8.470
16
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 57 8.389
17
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 60 8.351
18
P HRS035 Hirschsprung Disease 1 69 7.854
19
NRM005 Neuromuscular Disease 63 7.805
20
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 59 7.412
21
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 49 7.241
22
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 48 7.170
23
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 51 7.141
24
c CHR519 Charcot-Marie-Tooth Disease, Type 4b2 51 7.071
25
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 50 7.071
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