Search results for cnbp

103 hits were found for cnbp

# Family MCID Name MIFTS Score
1
c MYT020 Myotonic Dystrophy 2 57 36.584
2
P MYT002 Myotonic Dystrophy 51 16.852
3
P CTR002 Cataract 59 13.004
4
MYT011 Myotonia 38 11.792
5
P MYT023 Myotonia Congenita 56 11.286
6
P MYP004 Myopathy 67 10.732
7
FRN006 Frontotemporal Dementia 68 10.227
8
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 10.227
9
MYT003 Myotonic Disease 36 8.333
10
NRM005 Neuromuscular Disease 63 7.870
11
c MYT021 Myotonic Dystrophy 1 67 7.589
12
c SPN395 Spinal Muscular Atrophy, Type Ii 55 7.232
13
c HNT004 Huntington Disease-Like 2 51 7.232
14
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 7.232
15
NRM016 Neuromyotonia and Axonal Neuropathy, Autosomal Recessive 37 7.232
16
XLN191 X-Linked Hereditary Ataxia 19 7.232
17
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 7.232
18
c SPN304 Spinocerebellar Ataxia 8 47 7.232
19
OCL008 Oculopharyngeal Muscular Dystrophy 53 7.232
20
HYP052 Hyperkalemic Periodic Paralysis 62 7.232
21
MSC190 Muscular Disease 36 7.232
22
MSC004 Muscle Tissue Disease 21 7.232
23
IMM002 Immature Cataract 28 7.232
24
P LNS003 Lens Disease 33 7.232
25
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 7.232
26
c SPN314 Spinocerebellar Ataxia 10 47 7.232
27
P MYS005 Myositis 56 2.313
28
INC002 Inclusion Body Myositis 57 2.300
29
PPL052 Papillomatosis, Confluent and Reticulated 34 1.558
30
P MSC005 Muscular Dystrophy 66 1.514
31
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.444
32
SKN022 Skin Squamous Cell Carcinoma 54 1.444
33
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.444
34
P TRC072 Treacher Collins Syndrome 1 62 1.262
35
P TXP001 Toxoplasmosis 60 1.234
36
P OVR046 Ovarian Cyst 44 1.205
37
CLF027 Cleft Palate, Isolated 64 1.174
38
MST005 Mastitis 52 1.140
39
PRS047 Prostatitis 58 1.095
40
c MYT027 Myotonia Congenita, Autosomal Dominant 36 1.059
41
END021 Endomyocardial Fibrosis 56 1.059
42
c MYT029 Myotonia Congenita, Autosomal Recessive 42 1.059
43
P GST053 Gastric Cancer 82 1.008
44
SVR001 Severe Acute Respiratory Syndrome 68 1.008
45
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.766
46
BCK006 Back Pain 43 0.696
47
P MSC003 Muscular Atrophy 52 0.619
48
P BRS047 Breast Cancer 97 0.602
49
P PNC035 Pancreatic Cancer 86 0.602
50
ATM095 Autoimmune Disease 61 0.505
51
P CHR345 Chronic Pain 50 0.505
52
IMM167 Immune Deficiency Disease 77 0.452
53
HMN044 Human Immunodeficiency Virus Type 1 76 0.452
54
GST023 Gastric Ulcer 52 0.452
55
P GST044 Gastritis 55 0.452
56
AGN012 Agnathia-Otocephaly Complex 52 0.391
57
P FBR017 Fibrosarcoma 55 0.391
58
BRN050 Branchial Arch Defects 8 0.391
59
P MDL005 Medulloblastoma 75 0.357
60
P END033 Endocarditis 58 0.319
61
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.319
62
FBR047 Fibromyalgia 58 0.319
63
SPN020 Spondylosis 46 0.319
64
EMB004 Embryonal Carcinoma 55 0.319
65
OST016 Osteochondrosis 52 0.319
66
PRM329 Premature Aging 36 0.277
67
c FNC025 Fanconi Anemia, Complementation Group J 52 0.226
68
ANR009 Aneurysmal Bone Cysts 43 0.226
69
P SNS001 Sensorineural Hearing Loss 59 0.226
70
RCK004 Rickets 65 0.226
71
PRS014 Prostatic Cyst 19 0.226
72
URT001 Urethritis 52 0.226
73
AGN016 Aging 54 0.160
74
PRT013 Portal Hypertension 59 0.160
75
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.160
76
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.160
77
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.160
78
P RHM011 Rheumatoid Arthritis 81 0.160
79
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.160
80
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.160
81
P HNT016 Huntington Disease 73 0.160
82
HPT004 Hepatic Coma 43 0.160
83
CRD223 Cardiac Arrhythmia 63 0.160
84
P HPT023 Hepatocellular Carcinoma 95 0.160
85
LVR012 Liver Cirrhosis 62 0.160
86
P PRP019 Peripheral Nervous System Disease 57 0.160
87
P LTR001 Lateral Sclerosis 58 0.160
88
IMP005 Impotence 52 0.160
89
P AGM001 Agammaglobulinemia 67 0.160
90
HPT019 Hepatic Encephalopathy 59 0.160
91
P HYP086 Hypothyroidism 69 0.160
92
c DLT002 Dilated Cardiomyopathy 79 0.160
93
P NTR004 Neutropenia 62 0.160
94
P PLM036 Pulmonary Fibrosis 65 0.160
95
NND001 Nondystrophic Myotonia 19 0.160
96
ANX004 Anoxia 40 0.160
97
P DYS021 Dysautonomia 38 0.160
98
DYS073 Dysphagia 53 0.160
99
P TRM003 Tremor 50 0.160
100
P NRP001 Neuropathy 59 0.160
101
P PRG139 Progeroid Syndrome 29 0.160
102
IDP040 Idiopathic Eosinophilic Myositis 11 0.160
103
GNT082 Genetic Neuromuscular Disease 10 0.160
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