Search results for vapa

88 hits were found for vapa

# Family MCID Name MIFTS Score
1
c AMY091 Amyotrophic Lateral Sclerosis 1 87 13.436
2
FDB001 Foodborne Botulism 55 11.160
3
BRN014 Bronchopneumonia 52 9.443
4
c AMY090 Amyotrophic Lateral Sclerosis 8 44 8.253
5
MSN002 Mesenteric Lymphadenitis 30 8.171
6
P NRN021 Neuronal Ceroid Lipofuscinosis 64 8.171
7
ANS018 Anismus 29 7.891
8
c AMY023 Amyotrophic Lateral Sclerosis Type 6 36 7.891
9
WND001 Wound Botulism 34 7.891
10
INF006 Infant Botulism 43 7.891
11
c NNN020 Noonan Syndrome 7 39 7.891
12
HYP737 Hyperhidrosis, Gustatory 37 7.891
13
c SBC006 Subacute Leukemia 19 7.891
14
P LTR001 Lateral Sclerosis 57 2.276
15
P PNM007 Pneumonia 64 2.249
16
GST045 Gastroenteritis 58 1.416
17
P LNG064 Lung Cancer Susceptibility 3 69 1.239
18
P ADN016 Adenocarcinoma 63 1.239
19
c MJR022 Major Affective Disorder 8 37 1.207
20
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.207
21
c MJR024 Major Affective Disorder 9 40 1.207
22
P BPL003 Bipolar Disorder 56 1.207
23
STR067 Stroke, Ischemic 79 1.091
24
P MYS005 Myositis 55 0.811
25
OST017 Osteomyelitis 63 0.811
26
P CLR023 Colorectal Cancer 100 0.713
27
PLY150 Polykaryocytosis Inducer 29 0.647
28
P BRS047 Breast Cancer 97 0.551
29
P PNC035 Pancreatic Cancer 87 0.551
30
MYL005 Myelofibrosis 70 0.551
31
P SPN046 Spinal Muscular Atrophy 62 0.457
32
P MTR014 Motor Neuron Disease 65 0.457
33
P MSC003 Muscular Atrophy 52 0.457
34
ACQ007 Acquired Immunodeficiency Syndrome 58 0.428
35
47X002 47,xyy 47 0.428
36
ANR040 Aneurysm 60 0.428
37
TXC005 Toxic Shock Syndrome 61 0.396
38
SPN204 Spinal Muscular Atrophy, Late-Onset, Finkel Type 29 0.361
39
CHL123 Chlamydia 58 0.361
40
LYM021 Lymphadenitis 55 0.361
41
DWN001 Down Syndrome 70 0.323
42
c ORF040 Orofaciodigital Syndrome Viii 49 0.323
43
HMN044 Human Immunodeficiency Virus Type 1 76 0.323
44
CHR178 Chromosomal Triplication 33 0.323
45
DSS032 Disease by Infectious Agent 55 0.280
46
c HPT073 Hepatitis C Virus 70 0.280
47
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.280
48
IMM167 Immune Deficiency Disease 76 0.280
49
P DRR001 Diarrhea 55 0.280
50
GRN009 Granulomatous Hepatitis 34 0.280
51
c HPT001 Hepatitis C 61 0.280
52
P PRS040 Prostate Cancer 95 0.229
53
RTH007 Rothmund-Thomson Syndrome, Type 1 37 0.229
54
HLX001 Helix Syndrome 47 0.229
55
ENT011 Enterocolitis 55 0.229
56
P HPT021 Hepatitis 68 0.229
57
P END033 Endocarditis 58 0.229
58
NM001 Noma 37 0.229
59
PRT036 Peritonitis 65 0.229
60
CYT002 Cytokine Deficiency 43 0.229
61
ACT119 Acute Promyelocytic Leukemia 62 0.162
62
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.162
63
c LKM061 Leukemia, Acute Myeloid 83 0.162
64
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.162
65
P LKM062 Leukemia, Acute Lymphoblastic 69 0.162
66
P MYC007 Myocardial Infarction 69 0.162
67
c FRN060 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 6 28 0.162
68
P RSP003 Respiratory Failure 73 0.162
69
P PLY014 Polycystic Kidney Disease 71 0.162
70
P LKM002 Leukemia 65 0.162
71
HDR003 Hidradenitis 49 0.162
72
HST010 Histiocytosis 49 0.162
73
BCT022 Bacterial Infectious Disease 55 0.162
74
P END047 Endophthalmitis 53 0.162
75
P DYS005 Dyslexia 40 0.162
76
FCL010 Focal Epithelial Hyperplasia 36 0.162
77
GLS007 Glossitis 46 0.162
78
MRP001 Morphine Dependence 41 0.162
79
JPN002 Japanese Encephalitis 61 0.162
80
P AGG001 Aggressive Periodontitis 55 0.162
81
PLR005 Pleuropneumonia 33 0.162
82
P MYL006 Myeloid Leukemia 60 0.162
83
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.162
84
ATM077 Autoimmune Gastrointestinal Dysmotility 16 0.162
85
P ENC004 Encephalitis 61 0.162
86
c ACT075 Acute Myocardial Infarction 55 0.162
87
P PRD008 Periodontitis 63 0.162
88
SPL018 Splenomegaly 47 0.162
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