Search results for cpeb1

80 hits were found for cpeb1

# Family MCID Name MIFTS Score
1
PRM013 Premature Menopause 57 12.649
2
P FRG001 Fragile X Syndrome 70 10.398
3
SCL046 Scalp-Ear-Nipple Syndrome 50 8.738
4
c DMN019 Diamond-Blackfan Anemia 4 26 8.738
5
DSS008 Disease of Mental Health 74 8.738
6
P HPT023 Hepatocellular Carcinoma 95 2.492
7
GLB002 Glioblastoma 67 2.348
8
GLM045 Glioma 62 2.331
9
GLL048 Glial Tumor 51 2.331
10
P BRS047 Breast Cancer 97 2.030
11
AMN001 Amenorrhea 53 1.824
12
OST012 Osteoarthritis 77 1.747
13
SPN186 Spinal Cord Injury 60 1.466
14
END057 Endometrial Cancer 76 1.374
15
c ATS007 Autism Spectrum Disorder 71 1.327
16
P NRB001 Neuroblastoma 66 1.277
17
IRN008 Iron Overload in Africa 50 1.243
18
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 1.243
19
c HPT073 Hepatitis C Virus 70 1.243
20
RJS001 Ruijs-Aalfs Syndrome 47 1.243
21
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 1.243
22
ADL096 Adult Hepatocellular Carcinoma 60 1.243
23
HPT079 Hepatoid Adenocarcinoma 39 1.243
24
PDT042 Pediatric Hepatocellular Carcinoma 51 1.243
25
BRS099 Breast Ductal Carcinoma 61 1.243
26
P LNG021 Lung Occult Small Cell Carcinoma 20 1.243
27
LNG019 Lung Combined Type Small Cell Carcinoma 34 1.243
28
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.243
29
FBR086 Fibrolamellar Carcinoma 59 1.243
30
HPT011 Hepatocellular Clear Cell Carcinoma 46 1.243
31
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 1.243
32
PTY007 Pityriasis Rotunda 27 1.243
33
ANX010 Anxiety 70 1.221
34
P CHR345 Chronic Pain 50 1.221
35
HGH043 High Grade Glioma 46 1.190
36
IRR002 Irritable Bowel Syndrome 64 1.190
37
P GST053 Gastric Cancer 82 1.157
38
HLX001 Helix Syndrome 47 1.157
39
P LVR013 Liver Disease 68 1.157
40
PRT013 Portal Hypertension 59 1.157
41
AZS001 Azoospermia 45 1.157
42
P PRS040 Prostate Cancer 95 1.121
43
NNL006 Non-Alcoholic Steatohepatitis 54 1.121
44
CHL045 Choline Deficiency Disease 39 1.121
45
P HRP006 Herpes Simplex 65 1.081
46
DWN001 Down Syndrome 70 0.983
47
CHR178 Chromosomal Triplication 33 0.983
48
P BLD134 Bladder Cancer 79 0.913
49
c DPH024 Diaphragmatic Hernia, Congenital 63 0.701
50
P SCH015 Schizophrenia 74 0.533
51
P PNC035 Pancreatic Cancer 87 0.533
52
MYL005 Myelofibrosis 70 0.533
53
OST159 Osteogenic Sarcoma 66 0.376
54
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.238
55
MYL069 Myeloma, Multiple 76 0.238
56
P HYP069 Hyperparathyroidism 62 0.238
57
P INF032 Infertility 60 0.238
58
ING001 Inguinal Hernia 59 0.168
59
P ATS364 Autism 72 0.168
60
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.168
61
P OVR042 Ovarian Cancer 88 0.168
62
c SML038 Small Cell Cancer of the Lung 68 0.168
63
c PRM196 Premature Ovarian Failure 1 58 0.168
64
c SPS233 Spastic Ataxia 9, Autosomal Recessive 21 0.168
65
P MYC007 Myocardial Infarction 69 0.168
66
P LKM071 Leukemia, Chronic Lymphocytic 74 0.168
67
P GLM040 Glioma Susceptibility 1 70 0.168
68
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.168
69
P LNG064 Lung Cancer Susceptibility 3 69 0.168
70
MCS002 Mucositis 55 0.168
71
CHR494 Chromosome 15q25 Deletion Syndrome 17 0.168
72
MLG169 Malignant Astrocytoma 57 0.168
73
SQM006 Squamous Cell Carcinoma 59 0.168
74
P MLN007 Male Infertility 56 0.168
75
P TRN020 Turner Syndrome 67 0.168
76
P ADN016 Adenocarcinoma 63 0.168
77
P GND004 Gonadal Dysgenesis 46 0.168
78
P MLN008 Melanoma 75 0.168
79
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.168
80
CHR513 Chromosome 15q25.2 Microdeletion 5 0.168
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