Search results for egr2

69 hits were found for egr2

# Family MCID Name MIFTS Score
1
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 57 5.817
2
c CHR653 Charcot-Marie-Tooth Disease, Demyelinating, Type 1d 40 5.487
3
P CHR071 Charcot-Marie-Tooth Disease 65 5.473
4
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 51 4.899
5
CHR629 Charcot-Marie-Tooth Disease and Deafness 52 4.492
6
TTH006 Tooth Disease 46 4.169
7
CHR687 Charcot-Marie-Tooth Disease/hereditary Motor and Sensory Neuropathy 41 3.852
8
P NRP001 Neuropathy 56 3.819
9
P SCL018 Scoliosis 60 2.537
10
P PLY019 Polyneuropathy 56 2.537
11
P RTT002 Rett Syndrome 80 2.502
12
SNS003 Sensory Peripheral Neuropathy 54 2.502
13
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 59 2.461
14
P PRP019 Peripheral Nervous System Disease 58 1.956
15
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 56 1.836
16
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 1.794
17
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 1.794
18
NRP010 Neuropathy, Hereditary Motor and Sensory, Russe Type 36 1.794
19
CNT097 Central Hypoventilation Syndrome, Congenital 71 1.740
20
NRM005 Neuromuscular Disease 64 1.740
21
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 1.740
22
PRP066 Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease 51 1.740
23
c CHR647 Charcot-Marie-Tooth Disease, Demyelinating, Type 1c 46 1.740
24
c CHR376 Charcot-Marie-Tooth Disease, Type 4d 46 1.740
25
c CHR517 Charcot-Marie-Tooth Disease, Type 4a 45 1.740
26
PLX002 Plexiform Neurofibroma 44 1.740
27
c CHR670 Charcot-Marie-Tooth Disease, Demyelinating, Type 4f 43 1.740
28
c CHR657 Charcot-Marie-Tooth Disease, Axonal, Type 2j 39 1.740
29
c CHR641 Charcot-Marie-Tooth Disease, X-Linked Recessive, 2 34 1.740
30
P PPL023 Pupil Disease 28 1.740
31
c CHR026 Charcot-Marie-Tooth Disease Type X 25 1.740
32
ARG003 Argyll Robertson Pupil 22 1.740
33
ABN004 Abnormal Pupillary Function 15 1.740
34
ATM095 Autoimmune Disease 62 0.161
35
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.131
36
P GST053 Gastric Cancer 83 0.114
37
EWN003 Ewing Sarcoma 69 0.093
38
SRC014 Sarcoma 65 0.093
39
P BPL003 Bipolar Disorder 56 0.093
40
SPN035 Spindle Cell Sarcoma 53 0.093
41
c MJR024 Major Affective Disorder 9 41 0.093
42
c MJR022 Major Affective Disorder 8 38 0.093
43
c HRD088 Hereditary Neuropathies 37 0.093
44
c SYS001 Systemic Lupus Erythematosus 86 0.066
45
P LKM071 Leukemia, Chronic Lymphocytic 79 0.066
46
P SCH015 Schizophrenia 74 0.066
47
P NRB001 Neuroblastoma 72 0.066
48
P PHC003 Pheochromocytoma 71 0.066
49
P ATS364 Autism 70 0.066
50
P SYS005 Systemic Scleroderma 68 0.066
51
P INF038 Influenza 68 0.066
52
P MTR014 Motor Neuron Disease 65 0.066
53
c SCL052 Scleroderma, Familial Progressive 61 0.066
54
P LPS004 Lupus Erythematosus 61 0.066
55
THY029 Thyroid Carcinoma 59 0.066
56
VSL002 Visual Epilepsy 59 0.066
57
P SZR006 Seizure Disorder 56 0.066
58
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.066
59
P TRM003 Tremor 54 0.066
60
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.066
61
c CHR516 Charcot-Marie-Tooth Disease, Type 4c 50 0.066
62
HLX001 Helix Syndrome 47 0.066
63
ADR040 Adrenal Gland Pheochromocytoma 46 0.066
64
CRB004 Cerebral Artery Occlusion 45 0.066
65
P DMY001 Demyelinating Polyneuropathy 43 0.066
66
SYS071 Systemic Autoimmune Disease 37 0.066
67
P AXN001 Axonal Neuropathy 36 0.066
68
ADG002 Audiogenic Seizures 25 0.066
69
GJB007 Gjb1 Disorders: Charcot Marie Tooth Neuropathy and Central Nervous System Phenotypes 8 0.066
Content
Loading form....