Search results for egr2

31 hits were found for egr2

# Family MCID Name MIFTS Score
1
c CHR534 Charcot-Marie-Tooth Disease, Type 1d 38 6.506
2
NRP015 Neuropathy, Congenital Hypomyelinating 52 6.475
3
DJR004 Dejerine-Sottas Disease 46 5.696
4
P CHR071 Charcot-Marie-Tooth Disease 67 5.303
5
TTH006 Tooth Disease 52 4.927
6
P NRP001 Neuropathy 59 4.228
7
SNS003 Sensory Peripheral Neuropathy 45 3.910
8
c CHR537 Charcot-Marie-Tooth Disease, Type 1e 50 3.561
9
P CHR102 Charcot-Marie-Tooth Neuropathy 41 3.500
10
c CHR113 Charcot-Marie-Tooth Neuropathy Type 1 31 3.500
11
P RTT002 Rett Syndrome 77 3.429
12
WLM007 Wilms Tumor Susceptibility-5 63 3.386
13
CDQ001 Cauda Equina Syndrome 41 3.386
14
c CHR407 Charcot-Marie-Tooth Disease, Type 4f 38 3.386
15
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 2.765
16
c CHR530 Charcot-Marie-Tooth Disease, Type 2b 40 2.765
17
NRP016 Neuropathy, Recurrent, with Pressure Palsies 38 2.765
18
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 28 2.765
19
c CHR313 Charcot-Marie-Tooth Neuropathy Type 4f 19 2.765
20
GST053 Gastric Cancer 78 0.112
21
EWN003 Ewing Sarcoma 66 0.112
22
SRC014 Sarcoma 66 0.112
23
P BPL003 Bipolar Disorder 62 0.112
24
c SYS001 Systemic Lupus Erythematosus 86 0.079
25
P SCH015 Schizophrenia 77 0.079
26
P LPS004 Lupus Erythematosus 64 0.079
27
PNC041 Pancreatic Ductal Adenocarcinoma 64 0.079
28
P SCL018 Scoliosis 55 0.079
29
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 40 0.079
30
ADG002 Audiogenic Seizures 24 0.079
31
CNG102 Congenital Hypomyelination Neuropathy 18 0.079
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