Search results for oat.1

154 hits were found for oat.1

# Family MCID Name MIFTS Score
1
GYR003 Gyrate Atrophy of Choroid and Retina with or Without Ornithinemia 42 17.720
2
SML033 Small Cell Cancer of the Lung, Somatic 54 5.735
3
NRR002 Norrie Disease 60 4.248
4
EYD002 Eye Disease 61 4.201
5
CYS013 Cystinuria 63 3.638
6
LTT002 Letterer-Siwe Disease 56 3.638
7
RYS001 Reye Syndrome 52 3.638
8
CRB150 Cerebral Creatine Deficiency Syndrome 2 45 3.638
9
BRD003 Bird Fancier's Lung 40 3.638
10
PRP005 Parapsoriasis 39 3.638
11
HYP107 Hyperornithinemia-Hyperammonemia-Homocitrullinemia Syndrome 38 3.638
12
CRB148 Cerebral Creatine Deficiency Syndrome 3 36 3.638
13
RHM008 Rheumatic Myocarditis 35 3.638
14
CHR079 Choroid Disease 34 3.638
15
CRB137 Cerebral Creatine Deficiency Syndrome 27 3.638
16
c 3MT014 3-Methylglutaconic Aciduria, Type V 36 2.971
17
ORN004 Ornithinemia 20 2.971
18
PRS008 Prostate Small Cell Carcinoma 29 2.565
19
GLL007 Gallbladder Small Cell Carcinoma 22 2.565
20
ESP004 Esophagus Small Cell Carcinoma 14 2.565
21
EXT002 Extrahepatic Bile Duct Small Cell Adenocarcinoma 12 2.565
22
P CLC005 Celiac Disease 68 0.174
23
LPD008 Lipid Metabolism Disorder 58 0.129
24
GST050 Gastrointestinal System Disease 56 0.129
25
NTR005 Nutritional Deficiency Disease 36 0.129
26
DRM006 Dermatitis 66 0.117
27
P INT068 Intestinal Disease 60 0.117
28
P HRT032 Heart Disease 75 0.105
29
ETN001 Eating Disorder 58 0.105
30
CHY002 Chylomicron Retention Disease 57 0.105
31
CRC006 Carcinoid Syndrome 52 0.105
32
P DRM007 Dermatitis Herpetiformis 51 0.105
33
RDN001 Reading Disorder 34 0.105
34
P HYP607 Hypercholesterolemia, Familial 76 0.091
35
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.091
36
STM006 Stomach Disease 50 0.091
37
P FML035 Familial Hyperlipidemia 48 0.091
38
GLC008 Glucose Metabolism Disease 42 0.091
39
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.091
40
c CRN172 Coronary Heart Disease 3 19 0.091
41
c CLC045 Celiac Disease 2 17 0.091
42
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.074
43
P MYC007 Myocardial Infarction 79 0.074
44
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.074
45
HYP066 Hyperglycemia 61 0.074
46
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.074
47
WLL006 Wells Syndrome 59 0.074
48
CHL071 Child Syndrome 58 0.074
49
GLC003 Glucose Intolerance 55 0.074
50
KDS001 Kid Syndrome 53 0.074
51
FDL002 Food Allergy 53 0.074
52
GDS001 Good Syndrome 44 0.074
53
CHR008 Choroiditis 44 0.074
54
ANX004 Anoxia 43 0.074
55
GST078 Gastrointestinal Allergy 40 0.074
56
c CLC048 Celiac Disease 3 21 0.074
57
c CRN174 Coronary Heart Disease 2 20 0.074
58
c CLC037 Celiac Disease 4 20 0.074
59
c CRN175 Coronary Heart Disease 4 19 0.074
60
GLT030 Gluten Allergy 19 0.074
61
c CRN173 Coronary Heart Disease 8 18 0.074
62
P OBS005 Obesity 92 0.052
63
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.052
64
ULC004 Ulcerative Colitis 76 0.052
65
P CRN211 Coronary Artery Disease 74 0.052
66
CNG034 Congestive Heart Failure 72 0.052
67
SQM006 Squamous Cell Carcinoma 70 0.052
68
PRP027 Peripheral Vascular Disease 68 0.052
69
ISC006 Ischemic Heart Disease 68 0.052
70
P PNM007 Pneumonia 68 0.052
71
VSC007 Vascular Disease 67 0.052
72
ATH003 Atherosclerosis 65 0.052
73
DFC004 Deficiency Anemia 64 0.052
74
P INF037 Inflammatory Bowel Disease 63 0.052
75
P ATP001 Atopic Dermatitis 62 0.052
76
APH001 Aphthous Stomatitis 62 0.052
77
P RCK004 Rickets 61 0.052
78
TYP007 Typhoid Fever 61 0.052
79
c ACT075 Acute Myocardial Infarction 60 0.052
80
PLM033 Pulmonary Embolism 60 0.052
81
CLT003 Colitis 60 0.052
82
ALC006 Alcoholic Hepatitis 59 0.052
83
P THR015 Thrombophilia 59 0.052
84
GST045 Gastroenteritis 59 0.052
85
ART021 Arteriosclerosis 58 0.052
86
P HYP060 Hyperinsulinism 58 0.052
87
ART017 Aortic Disease 57 0.052
88
THR024 Thrombosis 57 0.052
89
P SML001 Small Cell Carcinoma 56 0.052
90
c THR092 Thrombophilia Due to Thrombin Defect 54 0.052
91
P THY032 Thyroiditis 54 0.052
92
CHL014 Cholera 53 0.052
93
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.052
94
KRT002 Keratomalacia 52 0.052
95
ALL026 Allergic Hypersensitivity Disease 52 0.052
96
IRN001 Iron Deficiency Anemia 52 0.052
97
c INF071 Inflammatory Bowel Disease 1 51 0.052
98
ATR060 Atrial Standstill, Digenic 51 0.052
99
VRC001 Varicocele 51 0.052
100
CLN019 Colonic Disease 51 0.052
101
ISL001 Islet Cell Tumor 50 0.052
102
RTN023 Retinitis 50 0.052
103
PLR008 Pleurisy 50 0.052
104
NNL002 Nonalcoholic Steatohepatitis 50 0.052
105
OST011 Osteomalacia 49 0.052
106
P FNC004 Fanconi Syndrome 49 0.052
107
LMB002 Lambert-Eaton Myasthenic Syndrome 49 0.052
108
SMT003 Somatostatinoma 48 0.052
109
c HMG001 Hemoglobin C Disease 47 0.052
110
VND001 Vein Disease 47 0.052
111
CRB025 Carbohydrate Metabolic Disorder 46 0.052
112
ART004 Aortic Atherosclerosis 46 0.052
113
BLD053 Blood Platelet Disease 46 0.052
114
SCR002 Scurvy 46 0.052
115
END072 Endotheliitis 42 0.052
116
IRN002 Iron Metabolism Disease 41 0.052
117
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.052
118
ONC003 Oncogenic Osteomalacia 41 0.052
119
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.052
120
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.052
121
c INF087 Inflammatory Bowel Disease 4 40 0.052
122
HYP391 Hyperammonemia 38 0.052
123
c INF086 Inflammatory Bowel Disease 3 38 0.052
124
ADJ001 Adjustment Disorder 38 0.052
125
SPC003 Specific Developmental Disorder 38 0.052
126
WTH001 Withdrawal Disorder 37 0.052
127
c HYP163 Hyperlipidemia Type 3 36 0.052
128
MDY003 Mody, Type Ii 36 0.052
129
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.052
130
LMB010 Lambert Syndrome 36 0.052
131
TRP004 Tropical Sprue 35 0.052
132
c INF089 Inflammatory Bowel Disease 6 34 0.052
133
P CRB059 Cerebellar Degeneration 34 0.052
134
FNC006 Functional Gastric Disease 32 0.052
135
c INF088 Inflammatory Bowel Disease 5 31 0.052
136
P ACT080 Acute Pulmonary Heart Disease 31 0.052
137
c HMG004 Hemoglobin D Disease 31 0.052
138
c INF078 Inflammatory Bowel Disease 2 31 0.052
139
VSC008 Vascular Hemostatic Disease 30 0.052
140
WHT017 Wheat Allergy 30 0.052
141
PRN032 Paraneoplastic Cerebellar Degeneration 30 0.052
142
VTM003 Vitamin Metabolic Disorder 30 0.052
143
c TRC078 Trichohepatoenteric Syndrome 2 29 0.052
144
c MYC058 Myocardial Infarction 2 28 0.052
145
c INF090 Inflammatory Bowel Disease 7 26 0.052
146
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.052
147
c SPN260 Spinal Muscular Atrophy, Lower Extremity-Predominant, 2, Ad 24 0.052
148
c INF093 Inflammatory Bowel Disease 14 23 0.052
149
c CRN214 Coronary Heart Disease 5 22 0.052
150
P CRN178 Coronary Heart Disease 6 21 0.052
151
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.052
152
c INF080 Inflammatory Bowel Disease 21 19 0.052
153
MLL015 Mills Syndrome 17 0.052
154
c DLT001 Delta Chain Disease 13 0.052
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