Search results for BA 1

301 hits were found for BA 1

# Family MCID Name MIFTS Score
1
P BPL003 Bipolar Disorder 59 0.164
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.162
3
c MJR024 Major Affective Disorder 9 42 0.161
4
c MJR022 Major Affective Disorder 8 39 0.161
5
HYP066 Hyperglycemia 63 0.161
6
ATM095 Autoimmune Disease 62 0.160
7
c HPT073 Hepatitis C Virus 74 0.159
8
c HPT001 Hepatitis C 62 0.149
9
P LNG032 Lung Cancer 99 0.140
10
P BRS047 Breast Cancer 99 0.138
11
c MCR113 Microvascular Complications of Diabetes 3 55 0.136
12
c MCR120 Microvascular Complications of Diabetes 7 48 0.136
13
c MCR130 Microvascular Complications of Diabetes 6 42 0.136
14
c MCR133 Microvascular Complications of Diabetes 4 42 0.136
15
P HPT021 Hepatitis 69 0.134
16
P RHB003 Rhabdomyosarcoma 62 0.134
17
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.132
18
c SPN225 Spondyloarthropathy 1 74 0.130
19
DPR016 Depression 64 0.125
20
LNG099 Lung Disease 62 0.124
21
ADL002 Adult Syndrome 62 0.123
22
MNT002 Mental Depression 60 0.122
23
GLB002 Glioblastoma 74 0.122
24
GLB015 Glioblastoma Multiforme 60 0.122
25
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.120
26
P ALZ034 Alzheimer Disease 90 0.120
27
48X005 48,xyyy 37 0.120
28
P LVR013 Liver Disease 71 0.119
29
P GLM045 Glioma 64 0.118
30
GLL048 Glial Tumor 48 0.117
31
HRW001 Hair Whorl 36 0.115
32
P KDN018 Kidney Disease 73 0.115
33
P CLR023 Colorectal Cancer 100 0.113
34
P LKM002 Leukemia 69 0.112
35
c HYP595 Hypertension, Essential 87 0.111
36
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.109
37
c HPT016 Hepatitis B 63 0.105
38
ANX010 Anxiety 75 0.104
39
P OVR042 Ovarian Cancer 89 0.103
40
P HPT023 Hepatocellular Carcinoma 99 0.103
41
P BLD134 Bladder Cancer 79 0.102
42
P PSR002 Psoriasis 63 0.102
43
PST011 Pustulosis of Palm and Sole 51 0.101
44
P MYL006 Myeloid Leukemia 61 0.101
45
END030 End Stage Renal Failure 60 0.099
46
c LKM061 Leukemia, Acute Myeloid 84 0.099
47
LVR012 Liver Cirrhosis 67 0.099
48
PLY150 Polykaryocytosis Inducer 31 0.098
49
CRV035 Cervical Cancer 77 0.098
50
P HRT032 Heart Disease 78 0.098
51
c SML038 Small Cell Cancer of the Lung 67 0.097
52
HLX001 Helix Syndrome 46 0.097
53
MYL069 Myeloma, Multiple 85 0.097
54
HYP266 Hypoxia 58 0.097
55
P DRR001 Diarrhea 55 0.096
56
ANR007 Anorexia Nervosa 64 0.096
57
ALC007 Alcohol Dependence 68 0.095
58
SPN051 Spondylitis 53 0.095
59
DRM006 Dermatitis 63 0.093
60
MLN008 Melanoma 68 0.092
61
c RHB024 Rhabdomyosarcoma 2 64 0.092
62
47X002 47,xyy 49 0.091
63
INF009 Inflammatory Spondylopathy 29 0.091
64
CNG034 Congestive Heart Failure 69 0.090
65
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.090
66
c HPT003 Hepatitis a 60 0.089
67
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.088
68
P BCL017 B-Cell Lymphoma 61 0.088
69
SKN016 Skin Disease 64 0.088
70
ISC004 Ischemia 62 0.088
71
P RHM011 Rheumatoid Arthritis 82 0.088
72
AST005 Asthma 80 0.087
73
PRT037 Pertussis 66 0.087
74
c PNS012 Paine Syndrome 61 0.085
75
P PRS038 Personality Disorder 66 0.085
76
c CHR684 Chronic Kidney Disease 68 0.084
77
HNS001 Hansen's Disease 35 0.084
78
P LPR021 Leprosy 3 67 0.084
79
ANR040 Aneurysm 60 0.083
80
P PLM037 Pulmonary Hypertension 69 0.083
81
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.083
82
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.082
83
P NSP012 Nasopharyngeal Carcinoma 67 0.082
84
VCC001 Vaccinia 50 0.082
85
P HYP086 Hypothyroidism 70 0.081
86
OST159 Osteogenic Sarcoma 67 0.081
87
BNR002 Bone Resorption Disease 51 0.081
88
P CHR345 Chronic Pain 52 0.080
89
FBR047 Fibromyalgia 60 0.080
90
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.080
91
END040 Endogenous Depression 55 0.079
92
P CRN018 Coronary Artery Anomaly 67 0.079
93
VRL011 Viral Infectious Disease 62 0.079
94
P CRN300 Coronary Heart Disease 1 59 0.079
95
ETN001 Eating Disorder 61 0.079
96
FTT001 Fatty Liver Disease 63 0.079
97
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.078
98
DFC004 Deficiency Anemia 77 0.078
99
PNG002 Pain Agnosia 52 0.078
100
P SCL018 Scoliosis 61 0.077
101
P ART022 Arthritis 71 0.077
102
NRT001 Neurotic Disorder 53 0.076
103
P EXN002 Exanthem 58 0.076
104
P ENC018 Encephalopathy 64 0.075
105
BRN071 Brain Injury 51 0.075
106
P NRF023 Neurofibromatosis, Type Ii 77 0.075
107
BLR001 Biliary Atresia 51 0.075
108
CHL123 Chlamydia 60 0.074
109
CRH001 Crohn's Disease 75 0.073
110
c FNC043 Fanconi Anemia, Complementation Group E 64 0.073
111
STM007 Stomatitis 51 0.073
112
P MJR001 Major Depressive Disorder 69 0.073
113
P HMP007 Hemophilia 58 0.073
114
OCL069 Ocular Motor Apraxia 53 0.073
115
IDP011 Idiopathic Interstitial Pneumonia 65 0.073
116
P PLM036 Pulmonary Fibrosis 66 0.072
117
P AST007 Astrocytoma 52 0.072
118
ULC004 Ulcerative Colitis 75 0.072
119
SKN019 Skin Melanoma 68 0.071
120
BCT022 Bacterial Infectious Disease 57 0.071
121
P RSP003 Respiratory Failure 75 0.071
122
MDD011 Mood Disorder 62 0.071
123
IRN002 Iron Metabolism Disease 58 0.071
124
CLT003 Colitis 63 0.071
125
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.071
126
DSS008 Disease of Mental Health 66 0.070
127
RCK004 Rickets 70 0.069
128
P ATS364 Autism 68 0.069
129
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.069
130
ANG054 Angina Pectoris 66 0.069
131
P PLV020 Pelvic Organ Prolapse 61 0.069
132
GST045 Gastroenteritis 60 0.069
133
c CNG216 Congenital Hydrocephalus 55 0.068
134
LNG031 Lung Benign Neoplasm 52 0.068
135
SCH014 Schistosomiasis 57 0.068
136
RHM027 Rheumatic Disease 56 0.068
137
P HYD006 Hydrocephalus 68 0.068
138
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.068
139
P ALP008 Alopecia 58 0.068
140
P DMN002 Dementia 68 0.068
141
PLM001 Pulmonary Tuberculosis 72 0.068
142
ALL003 Allergic Rhinitis 69 0.067
143
RRS014 Rare Surgical Neurologic Disease 33 0.067
144
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.067
145
P GST044 Gastritis 58 0.067
146
PRS045 Prostatic Hypertrophy 55 0.066
147
P HYP098 Hypereosinophilic Syndrome 67 0.066
148
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.066
149
c DNG003 Dengue Disease 61 0.066
150
PPL022 Papilloma 56 0.066
151
c HMP029 Hemophilia a 69 0.066
152
PRS021 Prostatic Adenoma 52 0.066
153
FCT001 Factor Viii Deficiency 54 0.065
154
ART002 Arts Syndrome 63 0.065
155
OST017 Osteomyelitis 65 0.065
156
PRS129 Prostatic Hyperplasia, Benign 49 0.065
157
P VSC011 Vasculitis 64 0.064
158
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.064
159
c ACT068 Acute Cystitis 63 0.064
160
P MYP006 Myopia 58 0.064
161
P SLP006 Sleep Apnea 71 0.064
162
CNS004 Constipation 59 0.064
163
P KLZ004 Kala-Azar 1 43 0.064
164
EYD002 Eye Disease 59 0.063
165
LSH001 Leishmaniasis 64 0.063
166
SQM002 Squamous Cell Papilloma 49 0.063
167
c OVR114 Ovarian Cancer 1 39 0.063
169
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.062
170
c ATS007 Autism Spectrum Disorder 69 0.062
171
PRP027 Peripheral Vascular Disease 72 0.062
172
c ACT071 Acute Kidney Failure 60 0.061
173
P HDC001 Headache 59 0.061
174
MYF002 Myofascial Pain Syndrome 39 0.061
175
PRP030 Purpura 56 0.061
176
PLL012 Pollen Allergy 46 0.060
177
DNT012 Dental Caries 52 0.060
178
MTB004 Metabolic Acidosis 48 0.060
179
MTH009 Mouth Disease 56 0.059
180
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.059
181
P HYP061 Hypertrophic Cardiomyopathy 68 0.058
182
DNG002 Dengue Hemorrhagic Fever 59 0.058
183
P RCT021 Rectum Cancer 54 0.057
184
c SVR001 Severe Acute Respiratory Syndrome 56 0.057
185
DYS015 Dysentery 45 0.057
186
IDP070 Idiopathic Scoliosis 39 0.057
187
THY030 Thyroid Gland Disease 53 0.057
188
CLR030 Clear Cell Renal Cell Carcinoma 54 0.057
189
P SBS003 Substance Abuse 56 0.056
190
P ART023 Arthropathy 61 0.056
191
P ANT006 Antiphospholipid Syndrome 56 0.056
192
c MLG074 Malignant Mesenchymoma 50 0.056
193
CYT018 Cytochrome P450 2d6 Variant 28 0.056
194
P SPN052 Spondyloarthropathy 54 0.055
195
BRL010 Buruli Ulcer 52 0.055
196
HND015 Hand Skill, Relative 33 0.055
197
PSY004 Psychotic Disorder 68 0.054
198
RFR003 Refractive Error 44 0.054
199
TRC008 Trachoma 49 0.053
200
c BPL002 Bipolar I Disorder 48 0.053
201
c BLC007 Bile Acid Synthesis Defect, Congenital, 1 43 0.053
202
BRN002 Bronchiolitis 60 0.053
203
c GLL024 Gallbladder Disease 1 53 0.053
204
P PYL005 Pyelonephritis 58 0.053
205
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 52 0.053
206
c BLC008 Bile Acid Synthesis Defect, Congenital, 2 32 0.053
207
P ALP009 Alopecia Areata 61 0.053
208
PLC008 Placenta Disease 51 0.052
209
INT007 Intermediate Coronary Syndrome 58 0.051
210
PLS011 Plasmacytoma 57 0.051
211
APN008 Apnea, Obstructive Sleep 64 0.051
212
AST006 Astigmatism 53 0.051
213
AMB001 Amebiasis 44 0.051
214
ANX004 Anoxia 44 0.051
215
INT002 Intermittent Claudication 60 0.050
216
HRY003 Hairy Cell Leukemia 57 0.049
217
FDB001 Foodborne Botulism 53 0.049
218
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.049
219
FRN006 Frontotemporal Dementia 70 0.049
220
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.049
221
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 65 0.049
222
AMB002 Amblyopia 51 0.049
223
ENT004 Enthesopathy 46 0.049
224
SPP007 Suppression Amblyopia 37 0.049
225
LNG039 Lung Squamous Cell Carcinoma 66 0.048
226
BLM002 Bulimia Nervosa 56 0.048
227
TST014 Testicular Cancer 49 0.048
228
P MJR007 Major Affective Disorder 1 44 0.047
229
EXP004 Exophthalmos 53 0.047
230
ANT024 Anthrax Disease 56 0.046
231
P OCL013 Oculodentodigital Dysplasia 65 0.046
232
QDR001 Quadriplegia 51 0.046
233
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 28 0.046
234
INF006 Infant Botulism 44 0.045
235
PST021 Postpartum Depression 51 0.045
236
PTY002 Pityriasis Versicolor 37 0.045
237
P MLN066 Melanoma, Cutaneous Malignant 1 69 0.045
238
CRC021 Carcinosarcoma 62 0.045
239
SCH003 Schizophreniform Disorder 49 0.044
240
INT052 Intestinal Volvulus 44 0.044
241
CHL122 Cholesteatoma of Middle Ear 52 0.044
242
AVD001 Avoidant Personality Disorder 45 0.044
243
c MJR008 Major Affective Disorder 2 35 0.043
244
LCK001 Locked-in Syndrome 46 0.043
245
OBS004 Obstructive Hydrocephalus 39 0.043
246
c MJR003 Major Affective Disorder 6 34 0.043
247
c MJR006 Major Affective Disorder 5 34 0.043
248
c MJR023 Major Affective Disorder 7 34 0.043
249
HDR002 Hidradenitis Suppurativa 58 0.043
250
CYS005 Cysticercosis 55 0.043
251
ONC002 Onchocerciasis 50 0.043
252
HDR003 Hidradenitis 48 0.043
253
BCL014 B-Cell Growth Factor 34 0.043
254
P GLL020 Gallbladder Disease 60 0.043
255
FBR009 Fibrous Dysplasia 47 0.043
256
c MJR004 Major Affective Disorder 4 29 0.043
257
SYS071 Systemic Autoimmune Disease 38 0.042
258
PRT018 Portal Vein Thrombosis 50 0.042
259
P DYS005 Dyslexia 42 0.042
260
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.042
261
APH001 Aphthous Stomatitis 56 0.041
262
STT041 Stuttering 53 0.041
263
BRN038 Bronchial Disease 53 0.041
264
NVS017 Nevus, Epidermal 66 0.041
265
P PRR016 Pierre Robin Syndrome 53 0.041
266
NNT012 Neonatal Jaundice 48 0.041
267
ART004 Aortic Atherosclerosis 47 0.040
268
OPD001 Opioid Abuse 42 0.040
269
GSG001 Gas Gangrene 52 0.040
270
DMP001 Dumping Syndrome 44 0.040
271
SPN119 Spondylarthropathy 45 0.039
272
P PST059 Pustular Psoriasis 39 0.039
273
c ACT004 Acute Diarrhea 38 0.039
274
P BRN120 Bronchus Cancer 45 0.039
275
DYS009 Dysthymic Disorder 48 0.038
276
SNL007 Senile Cataract 41 0.038
277
MLN065 Melanocytic Nevus Syndrome, Congenital 58 0.038
278
GRD001 Giardiasis 42 0.038
279
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.037
280
RTC010 Reticuloendotheliosis 37 0.037
281
CLS052 Classic Hairy Cell Leukemia 28 0.036
282
INT078 Intracranial Thrombosis 48 0.036
283
DYS002 Dysplastic Nevus Syndrome 42 0.035
284
GNT033 Genetic Prion Diseases 37 0.035
285
c ALP039 Alopecia Areata 1 23 0.035
286
BCL011 Bacillary Angiomatosis 25 0.034
287
BRJ001 Borjeson-Forssman-Lehmann Syndrome 53 0.034
288
ERY017 Erythema Elevatum Diutinum 45 0.034
289
MLN003 Melancholia 38 0.034
290
PLN026 Pilonidal Sinus 34 0.034
291
MLC004 Mulchandani-Bhoj-Conlin Syndrome 31 0.034
292
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 38 0.032
293
SPR020 Superficial Mycosis 35 0.032
294
SKN020 Skin Papilloma 31 0.032
295
CYC005 Cyclothymic Disorder 34 0.031
296
PRT112 Portal Hypertension, Noncirrhotic 31 0.031
297
CHR028 Chronic Wasting Disease 30 0.031
298
MNG001 Mongolian Spot 29 0.031
299
c ALB017 Albinism, Oculocutaneous, Type Vi 29 0.031
300
SML010 Simultanagnosia 27 0.031
301
c MNT273 Mental Retardation, Autosomal Dominant 44 25 0.031
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