Search results for lactose

677 hits were found for lactose

# Family MCID Name MIFTS Score
1
P LCT002 Lactose Intolerance 53 10.424
2
CNG304 Congenital Sucrase-Isomaltase Deficiency with Starch and Lactose Intolerance 9 5.569
3
c LCT011 Lactose Intolerance, Adult Type 26 4.481
4
LCT013 Lactase Deficiency, Congenital 45 3.702
5
P DRR001 Diarrhea 55 0.417
6
IRR002 Irritable Bowel Syndrome 65 0.253
7
HLX001 Helix Syndrome 47 0.241
8
P OVR082 Overgrowth Syndrome 50 0.155
9
GST045 Gastroenteritis 59 0.152
10
ULC004 Ulcerative Colitis 73 0.147
11
c ACT004 Acute Diarrhea 39 0.145
12
P OST002 Osteoporosis 74 0.142
13
CNS004 Constipation 58 0.139
14
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.139
15
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.139
16
P CLC063 Celiac Disease 1 66 0.137
17
P CTR002 Cataract 60 0.128
18
P INF037 Inflammatory Bowel Disease 54 0.119
19
c DRR009 Diarrhea 6 46 0.119
20
CRH001 Crohn's Disease 74 0.116
21
MST005 Mastitis 53 0.116
22
MLK006 Milk Allergy 48 0.109
23
P OVR042 Ovarian Cancer 88 0.106
24
HPT019 Hepatic Encephalopathy 60 0.106
25
P ENC018 Encephalopathy 61 0.102
26
P INT068 Intestinal Disease 53 0.099
27
P GLC113 Galactosemia I 64 0.095
28
RCK004 Rickets 68 0.091
29
ALL026 Allergic Hypersensitivity Disease 62 0.086
30
HPT004 Hepatic Coma 45 0.086
31
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.086
32
CLT003 Colitis 62 0.082
33
NTR005 Nutritional Deficiency Disease 62 0.082
34
CHL014 Cholera 59 0.082
35
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.077
36
AST005 Asthma 76 0.077
37
ADL002 Adult Syndrome 70 0.077
38
LNG099 Lung Disease 60 0.077
39
GST050 Gastrointestinal System Disease 56 0.077
40
GRD001 Giardiasis 45 0.077
41
KWS001 Kwashiorkor 44 0.077
42
48X005 48,xyyy 39 0.077
43
OVR094 Ovarian Epithelial Cancer 38 0.077
44
OSM001 Osmotic Diarrhea 32 0.077
45
P HPT023 Hepatocellular Carcinoma 100 0.072
46
P HRT032 Heart Disease 75 0.072
47
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.072
48
ANX010 Anxiety 73 0.072
49
DPR016 Depression 63 0.072
50
c PNS012 Paine Syndrome 61 0.072
51
MNT002 Mental Depression 58 0.072
52
PRT038 Protein-Energy Malnutrition 54 0.072
53
FDL002 Food Allergy 51 0.072
54
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.072
55
P PNC035 Pancreatic Cancer 84 0.067
56
CYS001 Cystic Fibrosis 81 0.067
57
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.067
58
P HYP086 Hypothyroidism 69 0.067
59
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.067
60
P HYP069 Hyperparathyroidism 63 0.067
61
c ACT068 Acute Cystitis 63 0.067
62
LPP008 Lipoprotein Quantitative Trait Locus 62 0.067
63
LVR012 Liver Cirrhosis 62 0.067
64
P SLM003 Salmonellosis 55 0.067
65
ART140 Arteries, Anomalies of 52 0.067
66
47X002 47,xyy 49 0.067
67
MTH071 Methane Production 26 0.067
68
P CLR023 Colorectal Cancer 99 0.061
69
P BRS047 Breast Cancer 97 0.061
70
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.061
71
c HYP595 Hypertension, Essential 84 0.061
72
P KDN018 Kidney Disease 72 0.061
73
c RHB024 Rhabdomyosarcoma 2 67 0.061
74
P MCR115 Microvascular Complications of Diabetes 5 66 0.061
75
CHY002 Chylomicron Retention Disease 65 0.061
76
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.061
77
TYP007 Typhoid Fever 63 0.061
78
DRM006 Dermatitis 61 0.061
79
P RTN018 Retinal Disease 53 0.061
80
OST011 Osteomalacia 52 0.061
81
DYS015 Dysentery 52 0.061
82
c SCN007 Secondary Hyperparathyroidism 51 0.061
83
GLC022 Glucose/galactose Malabsorption 45 0.061
84
CHL079 Children's Interstitial Lung Disease 26 0.061
85
OST012 Osteoarthritis 78 0.055
86
DFC004 Deficiency Anemia 70 0.055
87
P LVR013 Liver Disease 68 0.055
88
GST092 Gastroesophageal Reflux 67 0.055
89
MSL001 Measles 62 0.055
90
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.055
91
PPT005 Peptic Ulcer Disease 59 0.055
92
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 0.055
93
BLR008 Bilirubin Metabolic Disorder 57 0.055
94
MCL006 Macular Retinal Edema 55 0.055
95
HYP060 Hyperinsulinism 54 0.055
96
CRH005 Crohn's Colitis 53 0.055
97
P THY032 Thyroiditis 52 0.055
98
PNG002 Pain Agnosia 51 0.055
99
ENT011 Enterocolitis 51 0.055
100
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.055
101
DBT006 Diabetic Macular Edema 48 0.055
102
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.055
103
AMN006 Aminoaciduria 38 0.055
104
ACR005 Acrodermatitis 38 0.055
105
ENT007 Enteropathica 26 0.055
106
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.047
107
c CHR684 Chronic Kidney Disease 70 0.047
108
PLM001 Pulmonary Tuberculosis 69 0.047
109
c INF071 Inflammatory Bowel Disease 1 67 0.047
110
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.047
111
HYP056 Hypoglycemia 66 0.047
112
P PRS038 Personality Disorder 65 0.047
113
P ADL010 Adult Respiratory Distress Syndrome 65 0.047
114
P DBT009 Diabetes Mellitus 64 0.047
115
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.047
116
HYP066 Hyperglycemia 61 0.047
117
P PNC044 Pancreatitis 61 0.047
118
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.047
119
PRN019 Perinatal Necrotizing Enterocolitis 59 0.047
120
P URT039 Urticaria 58 0.047
121
NWB001 Newborn Respiratory Distress Syndrome 58 0.047
122
P HDC001 Headache 57 0.047
123
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.047
124
P CRD246 Cardiovascular System Disease 57 0.047
125
MTH009 Mouth Disease 56 0.047
126
AGN016 Aging 56 0.047
127
HYP005 Hypokalemia 55 0.047
128
P SHR001 Short Bowel Syndrome 53 0.047
129
DNT012 Dental Caries 53 0.047
130
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.047
131
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.047
132
NPH003 Nephrocalcinosis 51 0.047
133
MTB004 Metabolic Acidosis 50 0.047
134
SCR037 Sucrase-Isomaltase Deficiency, Congenital 50 0.047
135
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.047
136
CLN019 Colonic Disease 47 0.047
137
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.047
138
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.047
139
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.047
140
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.047
141
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.047
142
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.047
143
IMM003 Immunoglobulin Alpha Deficiency 45 0.047
144
DMP001 Dumping Syndrome 44 0.047
145
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.047
146
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.047
147
MRS001 Marasmus 42 0.047
148
ATX019 Ataxia with Vitamin E Deficiency 42 0.047
149
FNC002 Functional Diarrhea 41 0.047
150
PST092 Posttransplant Acute Limbic Encephalitis 29 0.047
151
P PRS040 Prostate Cancer 97 0.039
152
P ALZ034 Alzheimer Disease 88 0.039
153
P ATX030 Ataxia-Telangiectasia 82 0.039
154
MLR004 Malaria 81 0.039
155
IMM167 Immune Deficiency Disease 78 0.039
156
c ATR087 Atrial Standstill 1 75 0.039
157
c BTT014 Beta-Thalassemia 74 0.039
158
P NJM001 Nijmegen Breakage Syndrome 74 0.039
159
c SPN225 Spondyloarthropathy 1 73 0.039
160
P FML018 Familial Mediterranean Fever 73 0.039
161
P FML011 Familial Adenomatous Polyposis 72 0.039
162
P GRF003 Graft-Versus-Host Disease 72 0.039
163
OTT002 Otitis Media 72 0.039
164
DWN001 Down Syndrome 70 0.039
165
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.039
166
P ANG001 Angelman Syndrome 69 0.039
167
P LYM118 Lymphoma 68 0.039
168
P MYC084 Mycobacterium Tuberculosis 1 68 0.039
169
P INF038 Influenza 68 0.039
170
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.039
171
c MCR129 Microvascular Complications of Diabetes 1 66 0.039
172
ART001 Arterial Tortuosity Syndrome 66 0.039
173
AND002 Androgen Insensitivity Syndrome 66 0.039
174
CHG001 Chagas Disease 66 0.039
175
P DRM053 Dermatitis, Atopic 66 0.039
176
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.039
177
BRR014 Barrett Esophagus 65 0.039
178
PRT037 Pertussis 65 0.039
179
ATH013 Atherosclerosis Susceptibility 65 0.039
180
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.039
181
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.039
182
TBC004 Tobacco Addiction 64 0.039
183
GT001 Gout 64 0.039
184
BRC012 Brucellosis 64 0.039
185
P GCH001 Gaucher's Disease 63 0.039
186
P ANR048 Aniridia 1 63 0.039
187
P VSC007 Vascular Disease 63 0.039
188
c MLG084 Malignant Fibrous Histiocytoma 63 0.039
189
P CRN300 Coronary Heart Disease 1 63 0.039
190
ANR007 Anorexia Nervosa 63 0.039
191
c FNC043 Fanconi Anemia, Complementation Group E 62 0.039
192
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.039
193
P TRC086 Trichohepatoenteric Syndrome 1 62 0.039
194
ATM095 Autoimmune Disease 62 0.039
195
P ACR001 Aicardi-Goutieres Syndrome 62 0.039
196
P PRP029 Porphyria 62 0.039
197
CHL068 Cholestasis 61 0.039
198
OST003 Osteonecrosis 61 0.039
199
INT002 Intermittent Claudication 61 0.039
200
CHR066 Chronic Fatigue Syndrome 61 0.039
201
c ACT027 Acute Pancreatitis 60 0.039
202
ACN002 Acanthosis Nigricans 60 0.039
203
P THL005 Thalassemia 60 0.039
204
P BRN019 Bernard-Soulier Syndrome 60 0.039
205
P AXN002 Axenfeld-Rieger Syndrome 59 0.039
206
IRN001 Iron Deficiency Anemia 59 0.039
207
P HYP726 Hypercalcemia, Infantile, 1 58 0.039
208
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.039
209
BRS051 Breast Disease 58 0.039
210
DSS008 Disease of Mental Health 58 0.039
211
GLS018 Glass Syndrome 57 0.039
212
IRN002 Iron Metabolism Disease 57 0.039
213
APH001 Aphthous Stomatitis 57 0.039
214
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.039
215
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.039
216
FRC011 Fructose Intolerance, Hereditary 57 0.039
217
MCS002 Mucositis 56 0.039
218
P GST044 Gastritis 56 0.039
219
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.039
220
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.039
221
P GRV001 Graves' Disease 55 0.039
222
P ALP106 Alport Syndrome 1, X-Linked 55 0.039
223
ESN005 Eosinophilic Gastroenteritis 55 0.039
224
THR013 Thoracic Outlet Syndrome 54 0.039
225
P DDN001 Duodenal Ulcer 52 0.039
226
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.039
227
P MSC003 Muscular Atrophy 52 0.039
228
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.039
229
INT071 Intestinal Perforation 51 0.039
230
STM007 Stomatitis 50 0.039
231
TRY001 Trypanosomiasis 50 0.039
232
HYP017 Hypophosphatemia 50 0.039
233
CHL004 Cholelithiasis 49 0.039
234
BNR002 Bone Resorption Disease 48 0.039
235
ATS010 Autosomal Recessive Disease 48 0.039
236
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.039
237
SPL018 Splenomegaly 48 0.039
238
c GLC111 Galactosemia Ii 46 0.039
239
PRT019 Protein-Losing Enteropathy 45 0.039
240
P CHR345 Chronic Pain 44 0.039
241
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.039
242
c PCH010 Pachyonychia Congenita 3 44 0.039
243
MST019 Mastoiditis 43 0.039
244
LWC001 Low Compliance Bladder 43 0.039
245
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.039
246
CYT002 Cytokine Deficiency 42 0.039
247
CRB025 Carbohydrate Metabolic Disorder 41 0.039
248
GST020 Gastric Antral Vascular Ectasia 41 0.039
249
KLB003 Klebsiella Pneumonia 41 0.039
250
IMM080 Immunodeficiency 23 40 0.039
251
SMT020 Smith-Kingsmore Syndrome 38 0.039
252
BLN006 Blind Loop Syndrome 37 0.039
253
ATX010 Ataxia Neuropathy Spectrum 34 0.039
254
ALR002 Al-Raqad Syndrome 33 0.039
255
ACT064 Acute Necrotizing Encephalitis 33 0.039
256
c BLD140 Blood Group, I System 32 0.039
257
WHT017 Wheat Allergy 32 0.039
258
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.039
259
GST039 Gastroduodenitis 31 0.039
260
PLY150 Polykaryocytosis Inducer 31 0.039
261
RSP007 Respiratory Distress Syndrome, Infant 30 0.039
262
URT052 Urticaria, Aquagenic 21 0.039
263
BLD137 Blood Group--Ahonen 16 0.039
264
GSB001 Gas Bloat Syndrome 14 0.039
265
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.027
266
P GST053 Gastric Cancer 83 0.027
267
STR067 Stroke, Ischemic 81 0.027
268
c NRF023 Neurofibromatosis, Type Ii 80 0.027
269
INS024 Insulin-Like Growth Factor I 79 0.027
270
P PRK057 Parkinson Disease, Late-Onset 78 0.027
271
PHN003 Phenylketonuria 75 0.027
272
P RSP003 Respiratory Failure 74 0.027
273
END057 Endometrial Cancer 74 0.027
274
c HYP836 Hypercholesterolemia, Familial, 1 73 0.027
275
P MLT020 Multiple Sclerosis 72 0.027
276
HMN044 Human Immunodeficiency Virus Type 1 71 0.027
277
BHC003 Behcet Syndrome 71 0.027
278
P EPL164 Epilepsy 71 0.027
279
P ATS364 Autism 70 0.027
280
CNG034 Congestive Heart Failure 69 0.027
281
P ART022 Arthritis 69 0.027
282
ART016 Aortic Aneurysm 69 0.027
283
P MPL001 Maple Syrup Urine Disease 69 0.027
284
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.027
285
P PNM007 Pneumonia 68 0.027
286
CMM004 Common Variable Immunodeficiency 68 0.027
287
CNN005 Connective Tissue Disease 68 0.027
288
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.027
289
P THR014 Thrombocytopenia 67 0.027
290
P CHR012 Chronic Granulomatous Disease 67 0.027
291
P TRN020 Turner Syndrome 67 0.027
292
c MGR028 Migraine with or Without Aura 1 67 0.027
293
ALC007 Alcohol Dependence 66 0.027
294
ANG054 Angina Pectoris 66 0.027
295
P SKN015 Skin Carcinoma 66 0.027
296
P ATR011 Atrial Fibrillation 66 0.027
297
P MNN013 Meningitis 66 0.027
298
c FML001 Familial Atrial Fibrillation 65 0.027
299
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.027
300
P MCK013 Meckel Syndrome, Type 1 65 0.027
301
SRC014 Sarcoma 65 0.027
302
P MTR014 Motor Neuron Disease 65 0.027
303
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.027
304
c DBT099 Diabetes Mellitus, Type I 65 0.027
305
CLN015 Colon Adenocarcinoma 65 0.027
306
PRT036 Peritonitis 64 0.027
307
NRM005 Neuromuscular Disease 64 0.027
308
PLL001 Pallister-Hall Syndrome 64 0.027
309
P MST009 Mastocytosis 64 0.027
310
CTR172 Citrullinemia, Classic 64 0.027
311
P PRD008 Periodontitis 64 0.027
312
P ADN016 Adenocarcinoma 64 0.027
313
c PRC016 Pre-Eclampsia 63 0.027
314
PLG002 Plague 63 0.027
315
MSC152 Muscular Dystrophy, Becker Type 63 0.027
316
SKN016 Skin Disease 63 0.027
317
P SHR029 Short Syndrome 63 0.027
318
P PTT014 Pitt-Hopkins Syndrome 63 0.027
319
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.027
320
P EPL140 Epilepsy, Idiopathic Generalized 62 0.027
321
c HPT003 Hepatitis a 62 0.027
322
P LRS001 Larsen Syndrome 62 0.027
323
P ESP024 Esophagitis 62 0.027
324
P VSC011 Vasculitis 62 0.027
325
HSH003 Hashimoto Thyroiditis 62 0.027
326
TXC005 Toxic Shock Syndrome 62 0.027
327
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.027
328
P INT143 Interstitial Cystitis 61 0.027
329
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.027
330
FTT001 Fatty Liver Disease 61 0.027
331
c SCL052 Scleroderma, Familial Progressive 61 0.027
332
ALC006 Alcoholic Hepatitis 61 0.027
333
OSS012 Osseous Heteroplasia, Progressive 61 0.027
334
APP008 Appendicitis 61 0.027
335
DCB001 Decubitus Ulcer 61 0.027
336
NTH001 Netherton Syndrome 60 0.027
337
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.027
338
P SCL018 Scoliosis 60 0.027
339
P VNT002 Ventricular Septal Defect 60 0.027
340
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.027
341
ACQ007 Acquired Immunodeficiency Syndrome 60 0.027
342
STF001 Stiff-Person Syndrome 60 0.027
343
P OPT006 Optic Nerve Disease 60 0.027
344
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 59 0.027
345
P BND020 Bone Disease 59 0.027
346
BRN002 Bronchiolitis 59 0.027
347
ADN018 Adenoma 59 0.027
348
HLC007 Helicobacter Pylori Infection 59 0.027
349
ANR040 Aneurysm 59 0.027
350
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.027
351
PST028 Post-Traumatic Stress Disorder 58 0.027
352
FBR047 Fibromyalgia 58 0.027
353
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.027
354
P ALC033 Alcohol Use Disorder 58 0.027
355
c PRM005 Primary Hyperparathyroidism 58 0.027
356
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.027
357
ERY003 Erythema Multiforme 58 0.027
358
P CND004 Candidiasis 58 0.027
359
EXT034 Extrinsic Allergic Alveolitis 58 0.027
360
P GLL020 Gallbladder Disease 57 0.027
361
P ESP035 Esophagitis, Eosinophilic, 1 57 0.027
362
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.027
363
P EXN002 Exanthem 57 0.027
364
LYM021 Lymphadenitis 57 0.027
365
c ALZ056 Alzheimer Disease 3 57 0.027
366
P END033 Endocarditis 57 0.027
367
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.027
368
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.027
369
JPN002 Japanese Encephalitis 57 0.027
370
SCH014 Schistosomiasis 57 0.027
371
HYP266 Hypoxia 57 0.027
372
PHR003 Pharyngitis 57 0.027
373
AYM001 Ayme-Gripp Syndrome 57 0.027
374
c GLC112 Galactosemia Iii 56 0.027
375
P PYL005 Pyelonephritis 56 0.027
376
P MTC069 Mitochondrial Disorders 56 0.027
377
BCT022 Bacterial Infectious Disease 56 0.027
378
P SZR006 Seizure Disorder 56 0.027
379
PRS047 Prostatitis 56 0.027
380
DBL002 Double Outlet Right Ventricle 56 0.027
381
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.027
382
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.027
383
ORL005 Oral Candidiasis 56 0.027
384
BRN012 Bronchiolitis Obliterans 55 0.027
385
ZLL002 Zollinger-Ellison Syndrome 55 0.027
386
c BCT007 Bacterial Meningitis 55 0.027
387
NPH009 Nephrolithiasis 55 0.027
388
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.027
389
ACT058 Active Peptic Ulcer Disease 55 0.027
390
P SBS003 Substance Abuse 55 0.027
391
FLR002 Filariasis 55 0.027
392
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.027
393
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.027
394
PRP030 Purpura 54 0.027
395
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 54 0.027
396
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.027
397
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.027
398
CRY003 Cryptosporidiosis 54 0.027
399
BRN014 Bronchopneumonia 54 0.027
400
TND005 Tendinitis 54 0.027
401
AMN001 Amenorrhea 54 0.027
402
P LTR001 Lateral Sclerosis 54 0.027
403
CLL003 Cellulitis 54 0.027
404
NNL006 Non-Alcoholic Steatohepatitis 54 0.027
405
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.027
406
P INS002 in Situ Carcinoma 53 0.027
407
BCT002 Bacterial Vaginosis 53 0.027
408
BRN038 Bronchial Disease 53 0.027
409
P RTN016 Retinal Degeneration 53 0.027
410
c PRD040 Periodontitis, Chronic 53 0.027
411
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.027
412
ENC055 Encephalopathy, Ethylmalonic 53 0.027
413
LTR009 Lateral Meningocele Syndrome 53 0.027
414
c XNT010 Xanthinuria, Type I 53 0.027
415
INT075 Intracranial Hypertension 53 0.027
416
SPN035 Spindle Cell Sarcoma 53 0.027
417
c GLL024 Gallbladder Disease 1 53 0.027
418
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.027
419
c MCR113 Microvascular Complications of Diabetes 3 52 0.027
420
P LRY019 Laryngitis 52 0.027
421
c VRL010 Viral Hepatitis 52 0.027
422
P RCT021 Rectum Cancer 52 0.027
423
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.027
424
P ACT105 Acute Mountain Sickness 52 0.027
425
HYP014 Hyperuricemia 52 0.027
426
PPT001 Peptic Esophagitis 52 0.027
427
APR001 Apraxia 52 0.027
428
P OVR049 Ovarian Disease 52 0.027
429
OCL069 Ocular Motor Apraxia 51 0.027
430
c NMN014 Niemann-Pick Disease, Type C2 51 0.027
431
MLT134 Multiple Pterygium Syndrome, Lethal Type 51 0.027
432
MGL001 Megaloblastic Anemia 51 0.027
433
c PRM108 Primary Progressive Multiple Sclerosis 51 0.027
434
CLC001 Calciphylaxis 51 0.027
435
ACT049 Acute Disseminated Encephalomyelitis 51 0.027
436
ESP002 Esophageal Varix 51 0.027
437
P LSS002 Lissencephaly 51 0.027
438
CCC002 Coccidiosis 51 0.027
439
P THR015 Thrombophilia 51 0.027
440
DRR008 Diarrhea 1, Secretory Chloride, Congenital 51 0.027
441
BHR001 Behr Syndrome 51 0.027
442
PLR007 Pleural Empyema 50 0.027
443
P ECL001 Eclampsia 50 0.027
444
PST021 Postpartum Depression 50 0.027
445
HNT002 Hantavirus Pulmonary Syndrome 50 0.027
446
PYD002 Pyoderma 50 0.027
447
HRT011 Heart Septal Defect 50 0.027
448
P ATR005 Atrophic Gastritis 50 0.027
449
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.027
450
ENT004 Enthesopathy 49 0.027
451
KRT001 Keratoconjunctivitis Sicca 49 0.027
452
VGN020 Vaginal Disease 49 0.027
453
VLV047 Volvulus of Midgut 49 0.027
454
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.027
455
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 49 0.027
456
CCN002 Cocaine Abuse 49 0.027
457
BKR002 Baker-Gordon Syndrome 49 0.027
458
P CRV031 Cervical Adenocarcinoma 49 0.027
459
BRN071 Brain Injury 49 0.027
460
MTC005 Mitochondrial Metabolism Disease 49 0.027
461
DDN006 Duodenitis 49 0.027
462
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.027
463
URM002 Uremia 49 0.027
464
RYN001 Raynaud Disease 48 0.027
465
INT017 Intestinal Schistosomiasis 48 0.027
466
CCN001 Cocaine Dependence 48 0.027
467
ASP007 Aspiration Pneumonia 48 0.027
468
CLC006 Calcinosis 48 0.027
469
CLS016 Clostridium Difficile Colitis 48 0.027
470
GNG008 Ganglioneuroblastoma 48 0.027
471
HYP025 Hyperphosphatemia 48 0.027
472
P PRP056 Porphyria, Acute Hepatic 48 0.027
473
MLT006 Multidrug-Resistant Tuberculosis 48 0.027
474
HRN026 Hernia, Hiatus 47 0.027
475
DRY001 Dry Eye Syndrome 47 0.027
476
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 47 0.027
477
PRD004 Prediabetes Syndrome 47 0.027
478
ACT084 Acute Stress Disorder 47 0.027
479
c MCR120 Microvascular Complications of Diabetes 7 47 0.027
480
KRT002 Keratomalacia 47 0.027
481
P DNR001 Duane Retraction Syndrome 47 0.027
482
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.027
483
P OVR046 Ovarian Cyst 47 0.027
484
RYN005 Raynaud Phenomenon 47 0.027
485
BCK003 Background Diabetic Retinopathy 46 0.027
486
GNR003 Generalized Atherosclerosis 46 0.027
487
MDS022 Mediastinitis 46 0.027
488
MCR191 Microscopic Colitis 46 0.027
489
P ANX007 Anauxetic Dysplasia 1 46 0.027
490
P PLL002 Pellagra 46 0.027
491
CHD004 Chudley-Mccullough Syndrome 46 0.027
492
FLL008 Folliculitis 46 0.027
493
BST008 Bestrophinopathy, Autosomal Recessive 46 0.027
494
P HMR005 Hemorrhoid 46 0.027
495
c ACT042 Acute Pyelonephritis 46 0.027
496
BNS007 Bone Sarcoma 45 0.027
497
P HYP733 Hypercalciuria, Absorptive, 2 45 0.027
498
IMN001 Iminoglycinuria 45 0.027
499
P LSS036 Lissencephaly, X-Linked, 1 45 0.027
500
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.027
501
NWC001 Newcastle Disease 45 0.027
502
PRL008 Paralytic Ileus 45 0.027
503
URL001 Urolithiasis 45 0.027
504
SWN001 Swine Influenza 45 0.027
505
PRT030 Parathyroid Gland Disease 45 0.027
506
BLC012 Bile Acid Malabsorption, Primary 45 0.027
507
PNC085 Penicillin Allergy 45 0.027
508
CNT017 Central Nervous System Origin Vertigo 45 0.027
509
CLD007 Cold Agglutinin Disease 45 0.027
510
LNZ003 Lenz-Majewski Hyperostotic Dwarfism 45 0.027
511
ASP008 Aspiration Pneumonitis 45 0.027
512
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.027
513
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 44 0.027
514
HPT067 Hepatocellular Adenoma 44 0.027
515
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.027
516
GST027 Gastric Lymphoma 44 0.027
517
c PRM038 Primary Agammaglobulinemia 44 0.027
518
HPT082 Hepatic Adenomas, Familial 44 0.027
519
CHL109 Childhood Apraxia of Speech 44 0.027
520
CVD001 Covid-19 44 0.027
521
URT014 Ureterolithiasis 44 0.027
522
TND004 Tendinopathy 43 0.027
523
c EPL133 Epilepsy, Juvenile Absence 1 43 0.027
524
ICH002 Ichthyosis Bullosa of Siemens 43 0.027
525
c EPL026 Epileptic Encephalopathy, Early Infantile, 3 43 0.027
526
c ATM101 Autoimmune Gastritis 43 0.027
527
DNT001 Dental Fluorosis 43 0.027
528
MDD018 Middle East Respiratory Syndrome 43 0.027
529
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 42 0.027
530
P VND001 Vein Disease 42 0.027
531
c MCL066 Macular Dystrophy, Vitelliform, 2 42 0.027
532
DRG024 Drug Allergy 42 0.027
533
IMM154 Immunoglobulin a Deficiency 1 42 0.027
534
MYF002 Myofascial Pain Syndrome 42 0.027
535
FSC002 Fascioliasis 42 0.027
536
c HYP057 Hypervitaminosis D 42 0.027
537
IDP070 Idiopathic Scoliosis 42 0.027
538
GST095 Gastritis, Familial Giant Hypertrophic 41 0.027
539
LYM042 Lymphocytic Colitis 41 0.027
540
RST023 Resting Heart Rate, Variation in 41 0.027
541
XRP001 Xerophthalmia 41 0.027
542
49X006 49, Xxxxy Syndrome 41 0.027
543
c MCR130 Microvascular Complications of Diabetes 6 41 0.027
544
c MCR133 Microvascular Complications of Diabetes 4 41 0.027
545
EPD031 Epidermolysis Bullosa Simplex, Ogna Type 41 0.027
546
ACT088 Acute Insulin Response 41 0.027
547
EXT022 Exotropia 41 0.027
548
TRP004 Tropical Sprue 41 0.027
549
NNT008 Neonatal Abstinence Syndrome 41 0.027
550
c CNG413 Congenital Short Bowel Syndrome 41 0.027
551
c MCR112 Microvascular Complications of Diabetes 2 41 0.027
552
RDN001 Reading Disorder 40 0.027
553
c EPL027 Epileptic Encephalopathy, Early Infantile, 4 40 0.027
554
CWM001 Cow Milk Allergy 40 0.027
555
NRV004 Nerve Compression Syndrome 40 0.027
556
PRM020 Premenstrual Tension 40 0.027
557
PHS001 Phosphorus Metabolism Disease 40 0.027
558
ASP030 Aspirin Resistance 39 0.027
559
c PRG020 Paragangliomas 3 39 0.027
560
ULC007 Ulcerative Stomatitis 39 0.027
561
c DYS151 Dystonia 25 39 0.027
562
NRG003 Neurogenic Arthropathy 39 0.027
563
MNR003 Mineral Metabolism Disease 39 0.027
564
ADP007 Adie Pupil 39 0.027
565
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.027
566
BLR002 Bile Reflux 39 0.027
567
c MLG036 Malignant Spiradenoma 38 0.027
568
c OVR114 Ovarian Cancer 1 38 0.027
569
c DNR003 Duane Retraction Syndrome 1 38 0.027
570
TRC026 Tracheal Disease 38 0.027
571
CHL073 Cholestasis-Lymphedema Syndrome 38 0.027
572
BLR004 Biliary Dyskinesia 38 0.027
573
TXC001 Toxic Megacolon 38 0.027
574
HRT040 Hirata Disease 38 0.027
575
SCL001 Scalp Dermatosis 38 0.027
576
ATM052 Autoimmune Disease 1 37 0.027
577
c CRD082 Cardiomyopathy, Dilated, 1gg 37 0.027
578
BLN010 Balanitis 37 0.027
579
MLN070 Melanoma-Astrocytoma Syndrome 37 0.027
580
PST035 Postgastrectomy Syndrome 37 0.027
581
HYP026 Hypoglycemic Coma 36 0.027
582
c XLN227 X-Linked Chondrodysplasia Punctata 1 36 0.027
583
SPR007 Superior Mesenteric Artery Syndrome 36 0.027
584
ESN004 Eosinophilic Gastritis 36 0.027
585
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.027
586
PPT002 Peptic Ulcer Perforation 36 0.027
587
MDN008 Median Arcuate Ligament Syndrome 35 0.027
588
DNT046 Dental Abscess 35 0.027
589
TBR008 Tuberculous Peritonitis 35 0.027
590
FXD003 Fixed Drug Eruption 35 0.027
591
LMB008 Limb-Mammary Syndrome 35 0.027
592
DDN009 Duodenal Obstruction 34 0.027
593
c INT059 Internal Hemorrhoid 34 0.027
594
c LKM005 Leukemia, T-Cell, Chronic 34 0.027
595
PHY008 Physical Urticaria 34 0.027
596
c CHR057 Chronic Laryngitis 34 0.027
597
SLN001 Silent Myocardial Infarction 34 0.027
598
ALT003 Alternating Exotropia 34 0.027
599
PNC027 Pancreatic Gastrinoma 34 0.027
600
CHR067 Chronic Intestinal Vascular Insufficiency 33 0.027
601
LYM015 Lymphocytic Gastritis 33 0.027
602
DDN004 Duodenogastric Reflux 33 0.027
603
c PRS136 Prostate Cancer, Hereditary, 6 33 0.027
604
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.027
605
c PRS130 Prostate Cancer, Hereditary, 8 32 0.027
606
PNM003 Pneumatosis Cystoides Intestinalis 32 0.027
607
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 0.027
608
DLF001 Dieulafoy Lesion 32 0.027
609
CRT009 Critical Illness Polyneuropathy 32 0.027
610
GST013 Gastrojejunal Ulcer 32 0.027
611
RMN001 Rumination Disorder 31 0.027
612
JJN008 Jejunoileitis 31 0.027
613
GST007 Gastric Dilatation 31 0.027
614
CCL002 Cecal Disease 31 0.027
615
LRY007 Laryngeal Tuberculosis 31 0.027
616
EMP002 Emphysematous Cholecystitis 30 0.027
617
ISL119 Isolated Optic Neuritis 30 0.027
618
c ACT072 Acute Laryngitis 30 0.027
619
CLF051 Cleft Larynx, Posterior 30 0.027
620
MYC088 Mycobacterium Avium Complex Infections 29 0.027
621
DDN002 Duodenal Gastrinoma 29 0.027
622
ASC003 Ascending Cholangitis 29 0.027
623
PRM025 Primary Bacterial Infectious Disease 29 0.027
624
BLD041 Bladder Calculus 29 0.027
625
GST090 Gastroduodenal Crohn's Disease 29 0.027
626
IMM162 Immunoglobulin E Concentration, Serum 28 0.027
627
c ALP087 Alpha-Heavy Chain Disease 28 0.027
628
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.027
629
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.027
630
ARG004 Argyria 27 0.027
631
HNM002 Hinman Syndrome 27 0.027
632
OTL001 Outlet Dysfunction Constipation 27 0.027
633
URN022 Urinary Tract Infections, Recurrent 27 0.027
634
LRY026 Laryngeal Cleft 27 0.027
635
MLR020 Malaria, Mild 27 0.027
636
PGM030 Pigmentation Anomaly of the Skin 26 0.027
637
MST020 Mast Cell Activation Syndrome 26 0.027
638
ATM015 Autoimmune Disease of Gastrointestinal Tract 26 0.027
639
INT043 Intestinal Disaccharidase Deficiency 26 0.027
640
c MLG042 Malignant Otitis Externa 25 0.027
641
SQM005 Squamous Papillomatosis 25 0.027
642
FNC006 Functional Gastric Disease 25 0.027
643
URT049 Urate Oxidase, Pseudogene 25 0.027
644
MLN063 Melon Allergy 25 0.027
645
GRN011 Granulomatous Gastritis 25 0.027
646
CSC001 Cascade Stomach 25 0.027
647
c TRS025 Torsion Dystonia 2 24 0.027
648
BLD163 Blood Group, Dombrock System 24 0.027
649
HYD004 Hydrops of Gallbladder 24 0.027
650
P STR035 Streptococcal Group a Invasive Disease 23 0.027
651
ACQ006 Acquired Gastric Outlet Stenosis 23 0.027
652
DCL001 Diclofenac Allergy 23 0.027
653
ESP016 Esophagus Melanoma 23 0.027
654
NCR005 Necrotizing Gastritis 23 0.027
655
DSC013 Discrimination, Two-Point, Reduction in 23 0.027
656
VGS001 Vagus Nerve Disease 23 0.027
657
CRV010 Cervix Erosion 23 0.027
658
CFR002 Cefuroxime Allergy 22 0.027
659
LNG018 Lingual Goiter 22 0.027
660
FNG003 Fungal Esophagitis 22 0.027
661
BNZ003 Benzylpenicillin Allergy 22 0.027
662
LKN005 Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema 22 0.027
663
ANG012 Angiodysplasia of Intestine 21 0.027
664
GST031 Gastric Gastrinoma 21 0.027
665
DSP001 Displacement of Cardia Through Esophageal Hiatus 21 0.027
666
BLD165 Blood Group, Colton System 20 0.027
667
MTR027 Mitral Atresia 20 0.027
668
INF036 Inflammatory and Toxic Neuropathy 20 0.027
669
c BCT001 Bacterial Esophagitis 20 0.027
670
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.027
671
AND005 Androgen Insensitivity Syndrome, Mild 19 0.027
672
AQG001 Aquagenic Pruritus 19 0.027
673
GLT030 Gluten Allergy 19 0.027
674
CHR009 Chronic Duodenal Ileus 18 0.027
675
HMN011 Hemangioma of Intra-Abdominal Structure 17 0.027
676
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 17 0.027
677
GTM001 Goat Milk Allergy 10 0.027
Content
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