Search results for aida

159 hits were found for aida

# Family MCID Name MIFTS Score
1
ACT119 Acute Promyelocytic Leukemia 62 10.866
2
P LKM002 Leukemia 67 8.048
3
P DRR001 Diarrhea 55 4.913
4
P MYC007 Myocardial Infarction 70 4.867
5
P PRS038 Personality Disorder 65 4.580
6
AVD001 Avoidant Personality Disorder 49 4.515
7
P MMP001 Mumps 57 4.288
8
BRD004 Borderline Personality Disorder 53 3.261
9
ATR057 Atrioventricular Block 54 3.159
10
SNT005 Sinoatrial Node Disease 47 3.159
11
P SCK002 Sick Sinus Syndrome 55 3.159
12
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.072
13
SPN186 Spinal Cord Injury 61 2.996
14
P MSC003 Muscular Atrophy 52 2.944
15
P SPN046 Spinal Muscular Atrophy 63 2.944
16
P MYC008 Myocarditis 59 2.918
17
c TYP008 Type 1 Diabetes Mellitus 70 2.744
18
SPR004 Supravalvular Aortic Stenosis 57 2.542
19
CNG034 Congestive Heart Failure 69 2.425
20
ART140 Arteries, Anomalies of 53 2.403
21
LPP008 Lipoprotein Quantitative Trait Locus 65 2.403
22
CHL014 Cholera 62 2.262
23
PTH003 Pathologic Nystagmus 52 2.262
24
P HDC001 Headache 57 2.156
25
PRC013 Pericarditis 53 2.144
26
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.016
27
AMN003 Amnestic Disorder 54 2.016
28
TRM010 Traumatic Brain Injury 51 1.986
29
PRT037 Pertussis 65 1.893
30
48X005 48,xyyy 39 1.893
31
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.875
32
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.875
33
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.875
34
c PRG042 Progressive Familial Heart Block, Type Ia 66 1.875
35
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.875
36
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.875
37
THR024 Thrombosis 56 1.875
38
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.875
39
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.875
40
c ATR092 Atrial Fibrillation, Familial, 15 23 1.875
41
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.875
42
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.875
43
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.875
44
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.875
45
c LKM061 Leukemia, Acute Myeloid 83 1.796
46
c ATS007 Autism Spectrum Disorder 72 1.714
47
P ATT013 Attention Deficit-Hyperactivity Disorder 64 1.714
48
P SZR006 Seizure Disorder 70 1.584
49
c ATR087 Atrial Standstill 1 74 1.584
50
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 1.584
51
P MYL006 Myeloid Leukemia 61 1.584
52
P NTR004 Neutropenia 63 1.584
53
SVR004 Severe Combined Immunodeficiency 72 1.584
54
P PNM007 Pneumonia 67 1.584
55
HMP009 Haemophilus Influenzae 41 1.467
56
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.339
57
BRN071 Brain Injury 50 1.339
58
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.276
59
c MCR130 Microvascular Complications of Diabetes 6 41 1.276
60
RSP021 Respiratory Allergy 41 1.276
62
c MCR120 Microvascular Complications of Diabetes 7 47 1.276
63
c MCR113 Microvascular Complications of Diabetes 3 52 1.276
64
c MCR133 Microvascular Complications of Diabetes 4 41 1.276
65
P VSC007 Vascular Disease 63 1.276
66
MCS002 Mucositis 56 1.276
67
HYP056 Hypoglycemia 65 1.276
68
P HML002 Hemolytic Anemia 62 1.198
69
ALL029 Allergic Disease 59 1.198
70
TRP006 Tarp Syndrome 58 1.037
71
CYS001 Cystic Fibrosis 78 1.037
72
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.037
73
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.037
74
P RTN024 Retinoblastoma 73 1.037
75
LYM017 Lyme Disease 62 1.037
76
GST050 Gastrointestinal System Disease 55 1.037
77
PRD013 Periodic Fever, Familial, Autosomal Dominant 68 0.958
78
P AMY004 Amyloidosis 70 0.958
79
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.847
80
P OVR082 Overgrowth Syndrome 49 0.847
81
DFC004 Deficiency Anemia 74 0.847
82
P SLM003 Salmonellosis 54 0.847
83
c CTR103 Cataract 4, Multiple Types 48 0.847
84
INT303 Intracranial Hypertension, Idiopathic 56 0.847
85
P ART023 Arthropathy 61 0.847
86
c ACT004 Acute Diarrhea 40 0.847
87
PLC002 Plica Syndrome 35 0.847
88
IRN001 Iron Deficiency Anemia 58 0.847
89
BRC012 Brucellosis 66 0.847
90
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.847
91
SYN007 Synovitis 55 0.847
92
IRN002 Iron Metabolism Disease 57 0.847
93
STT001 Status Epilepticus 59 0.847
94
c LKM005 Leukemia, T-Cell, Chronic 34 0.847
95
ART109 Arterial Thoracic Outlet Syndrome 25 0.846
96
ALN001 Aland Island Eye Disease 55 0.846
97
AGN016 Aging 54 0.846
98
P CLR023 Colorectal Cancer 100 0.846
99
CLR108 Colorectal Adenoma 64 0.846
100
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.846
101
P ANR048 Aniridia 1 64 0.846
102
ADN018 Adenoma 59 0.846
103
PPL001 Papillary Adenoma 44 0.846
104
ATM021 Autoimmune Inner Ear Disease 36 0.846
105
P BRS047 Breast Cancer 98 0.811
106
PRT251 Proteinuria, Chronic Benign 57 0.677
107
OST012 Osteoarthritis 77 0.677
108
P ALZ034 Alzheimer Disease 87 0.599
109
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.599
110
P FRG001 Fragile X Syndrome 70 0.599
111
P LPR021 Leprosy 3 71 0.599
112
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.599
113
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.599
114
ATM095 Autoimmune Disease 61 0.599
115
c MGR028 Migraine with or Without Aura 1 64 0.599
116
HMN044 Human Immunodeficiency Virus Type 1 78 0.599
117
EXR010 Exercise-Induced Bronchoconstriction 34 0.599
118
OCL069 Ocular Motor Apraxia 57 0.599
119
c HYP836 Hypercholesterolemia, Familial, 1 73 0.599
120
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 0.599
121
P HML001 Hemolytic-Uremic Syndrome 52 0.599
122
c ACT073 Acute Leukemia 58 0.599
123
P OPN001 Open-Angle Glaucoma 55 0.599
124
OCL006 Ocular Hypertension 53 0.599
125
ADG002 Audiogenic Seizures 25 0.599
126
SVR001 Severe Acute Respiratory Syndrome 67 0.599
127
P ANT006 Antiphospholipid Syndrome 55 0.599
128
P CHR012 Chronic Granulomatous Disease 69 0.599
129
SCR003 Secretory Diarrhea 35 0.599
130
CHG001 Chagas Disease 66 0.599
131
c ACT068 Acute Cystitis 61 0.599
132
TXC005 Toxic Shock Syndrome 62 0.599
133
P AML002 Amelogenesis Imperfecta 56 0.599
134
P HRT032 Heart Disease 81 0.599
135
TTN003 Tetanus 65 0.599
136
PLR005 Pleuropneumonia 33 0.599
137
HNS001 Hansen's Disease 32 0.599
138
P CRN300 Coronary Heart Disease 1 73 0.598
139
P MYC084 Mycobacterium Tuberculosis 1 68 0.598
140
CLT003 Colitis 63 0.598
141
CRH005 Crohn's Colitis 53 0.598
142
c BSL024 Basal Cell Carcinoma 1 55 0.598
143
c INF071 Inflammatory Bowel Disease 1 65 0.598
144
SCH036 Scheie Syndrome 73 0.598
145
c HYP724 Hyperlipoproteinemia, Type Iii 67 0.598
146
CRH001 Crohn's Disease 80 0.598
147
SKN019 Skin Melanoma 71 0.598
148
ULC004 Ulcerative Colitis 74 0.598
149
P TRN020 Turner Syndrome 67 0.598
150
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.598
151
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.598
152
P MLN008 Melanoma 76 0.598
153
c BSL007 Basal Cell Carcinoma 68 0.598
154
SKN013 Skin Benign Neoplasm 50 0.598
155
P RCT021 Rectum Cancer 54 0.598
156
AND005 Androgen Insensitivity Syndrome, Mild 21 0.598
157
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.598
158
P ATS364 Autism 69 0.573
159
P LKM062 Leukemia, Acute Lymphoblastic 69 0.573
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