Search results for egr2

32 hits were found for egr2

# Family MCID Name MIFTS Score
1
c CHR653 Charcot-Marie-Tooth Disease, Demyelinating, Type 1d 36 6.132
2
CHR629 Charcot-Marie-Tooth Disease and Deafness 42 6.020
3
NRP060 Neuropathy, Congenital Hypomyelinating or Amyelinating, Autosomal Recessive 50 6.019
4
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 45 5.869
5
P CHR071 Charcot-Marie-Tooth Disease 65 5.411
6
TTH006 Tooth Disease 53 4.610
7
P NRP001 Neuropathy 63 4.307
8
c CHR113 Charcot-Marie-Tooth Neuropathy Type 1 27 2.873
9
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 2.824
10
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 54 2.824
11
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 48 2.824
12
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 47 2.824
13
CDQ001 Cauda Equina Syndrome 40 2.824
14
c CHR646 Charcot-Marie-Tooth Disease, Axonal, Type 2b 39 2.824
15
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 29 2.824
16
c CHR489 Charcot-Marie-Tooth Disease, Axonal, Type 2q 28 2.824
17
PRP019 Peripheral Nervous System Disease 60 2.112
18
GST053 Gastric Cancer 77 0.136
19
EWN003 Ewing Sarcoma 68 0.111
20
SRC014 Sarcoma 68 0.111
21
P BPL003 Bipolar Disorder 59 0.111
22
P HPT023 Hepatocellular Carcinoma 94 0.079
23
c SYS001 Systemic Lupus Erythematosus 86 0.079
24
P RTT002 Rett Syndrome 82 0.079
25
P ATS364 Autism 70 0.079
26
P SCH015 Schizophrenia 69 0.079
27
P LPS004 Lupus Erythematosus 68 0.079
28
c SCL052 Scleroderma, Familial Progressive 64 0.079
29
P SCL018 Scoliosis 55 0.079
30
PNC041 Pancreatic Ductal Adenocarcinoma 52 0.079
31
ADG002 Audiogenic Seizures 26 0.079
32
CNG102 Congenital Hypomyelination Neuropathy 22 0.079
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