Search results for mannose

701 hits were found for mannose

# Family MCID Name MIFTS Score
1
MNN034 Mannose-Binding Lectin Deficiency 45 7.899
2
MNN041 Mannose-Binding Lectin Protein Deficiency 14 4.400
3
MNN046 Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type 9 3.566
4
QLT036 Qualitative or Quantitative Defects of Protein O-Mannose Beta1,2n-Acetylglucosaminyltransferase 2 2.521
5
c SYS001 Systemic Lupus Erythematosus 86 0.220
6
ATM095 Autoimmune Disease 61 0.198
7
IMM167 Immune Deficiency Disease 78 0.189
8
P LPS004 Lupus Erythematosus 61 0.179
9
P RHM011 Rheumatoid Arthritis 80 0.161
10
HMN044 Human Immunodeficiency Virus Type 1 71 0.154
11
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.149
12
BCT022 Bacterial Infectious Disease 56 0.147
13
P CND004 Candidiasis 57 0.141
14
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.139
15
P MYC084 Mycobacterium Tuberculosis 1 68 0.139
16
P NTR004 Neutropenia 63 0.139
17
LSH001 Leishmaniasis 63 0.136
18
c ACT068 Acute Cystitis 63 0.136
19
P KLZ004 Kala-Azar 1 41 0.136
20
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 31 0.136
21
TXC005 Toxic Shock Syndrome 61 0.133
22
c HPT016 Hepatitis B 59 0.131
23
P PNM007 Pneumonia 68 0.128
24
NSS002 Neisseria Meningitidis Infection 46 0.128
25
CYS001 Cystic Fibrosis 80 0.119
26
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.119
27
LYS002 Lysosomal Storage Disease 52 0.119
28
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.116
29
ATH013 Atherosclerosis Susceptibility 66 0.116
30
P DRR001 Diarrhea 57 0.116
31
P GCH001 Gaucher's Disease 64 0.112
32
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.109
33
CHL123 Chlamydia 59 0.109
34
P PYL005 Pyelonephritis 56 0.109
35
VRL011 Viral Infectious Disease 61 0.105
36
CHL014 Cholera 55 0.105
37
P MCL001 Mucolipidosis 47 0.105
38
P LVR013 Liver Disease 68 0.102
39
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.102
40
LVR012 Liver Cirrhosis 63 0.102
41
VSC003 Visceral Leishmaniasis 55 0.102
42
c GCH015 Gaucher Disease, Type I 70 0.098
43
P MNN013 Meningitis 65 0.098
44
VLV011 Vulvovaginal Candidiasis 51 0.098
45
CYT002 Cytokine Deficiency 44 0.098
46
PLM001 Pulmonary Tuberculosis 70 0.094
47
P BRN022 Bronchiectasis 59 0.094
48
P CYS018 Cystitis 59 0.094
49
END030 End Stage Renal Failure 58 0.094
50
STM007 Stomatitis 49 0.094
51
P HPT023 Hepatocellular Carcinoma 100 0.090
52
KRT019 Keratitis, Hereditary 67 0.090
53
P MSC005 Muscular Dystrophy 66 0.090
54
PRT036 Peritonitis 65 0.090
55
CLN015 Colon Adenocarcinoma 63 0.090
56
LNG099 Lung Disease 61 0.090
57
PPL052 Papillomatosis, Confluent and Reticulated 34 0.090
58
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.090
59
CRH001 Crohn's Disease 74 0.086
60
P ASP006 Aspergillosis 66 0.086
61
CHG001 Chagas Disease 66 0.086
62
c RHB024 Rhabdomyosarcoma 2 65 0.086
63
PRT037 Pertussis 65 0.086
64
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.086
65
47X002 47,xyy 49 0.086
66
HMP009 Haemophilus Influenzae 42 0.086
67
P BRS047 Breast Cancer 96 0.082
68
OTT002 Otitis Media 71 0.082
69
c HPT073 Hepatitis C Virus 70 0.082
70
HYP056 Hypoglycemia 66 0.082
71
P DNG005 Dengue Virus 57 0.082
72
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.082
73
P GLM007 Glomerulonephritis 57 0.082
74
c MCR113 Microvascular Complications of Diabetes 3 52 0.082
75
BCT004 Bacteriuria 48 0.082
76
IGG001 Iga Glomerulonephritis 48 0.082
77
c MCR120 Microvascular Complications of Diabetes 7 47 0.082
78
CHL147 Chlamydia Pneumonia 45 0.082
79
GLL048 Glial Tumor 45 0.082
80
c MCR130 Microvascular Complications of Diabetes 6 41 0.082
81
c MCR133 Microvascular Complications of Diabetes 4 41 0.082
82
48X005 48,xyyy 39 0.082
83
ACN019 Acanthamoeba Keratitis 31 0.082
84
c GLY008 Glycogen Storage Disease Ii 70 0.077
85
P LKM002 Leukemia 66 0.077
86
P HRP006 Herpes Simplex 65 0.077
87
c PRC016 Pre-Eclampsia 63 0.077
88
P GLM045 Glioma 63 0.077
89
SCH014 Schistosomiasis 56 0.077
90
P LYM031 Lymphocytic Leukemia 55 0.077
91
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.077
92
KRT002 Keratomalacia 48 0.077
93
MNN032 Meningococcal Meningitis 46 0.077
94
c CNG189 Congenital Disorder of Glycosylation, Type Ib 43 0.077
95
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.077
96
P CLR023 Colorectal Cancer 98 0.072
97
P LKM062 Leukemia, Acute Lymphoblastic 68 0.072
98
c HPT001 Hepatitis C 63 0.072
99
P VSC011 Vasculitis 62 0.072
100
ISC004 Ischemia 60 0.072
101
CYT008 Cytomegalovirus Infection 56 0.072
102
P INF037 Inflammatory Bowel Disease 56 0.072
103
PRT019 Protein-Losing Enteropathy 46 0.072
104
URN022 Urinary Tract Infections, Recurrent 26 0.072
105
MLR004 Malaria 80 0.067
106
AST005 Asthma 77 0.067
107
c SPN225 Spondyloarthropathy 1 73 0.067
108
P ART022 Arthritis 70 0.067
109
P INF038 Influenza 68 0.067
110
CMM004 Common Variable Immunodeficiency 67 0.067
111
KWS002 Kawasaki Disease 64 0.067
112
P MYP004 Myopathy 64 0.067
113
P ADN016 Adenocarcinoma 64 0.067
114
RHM001 Rheumatic Fever 61 0.067
115
c DNG003 Dengue Disease 59 0.067
116
BRN002 Bronchiolitis 59 0.067
117
ENT011 Enterocolitis 50 0.067
118
P SCK005 Sickle Cell Disease 50 0.067
119
HLX001 Helix Syndrome 47 0.067
120
c CHR098 Chronic Pyelonephritis 35 0.067
121
P PNC035 Pancreatic Cancer 84 0.061
122
P GST053 Gastric Cancer 83 0.061
123
P BLD134 Bladder Cancer 78 0.061
124
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.061
125
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.061
126
BHC003 Behcet Syndrome 70 0.061
127
BRN024 Bronchitis 68 0.061
128
c JVN010 Juvenile Rheumatoid Arthritis 67 0.061
129
P MCR115 Microvascular Complications of Diabetes 5 66 0.061
130
ALL026 Allergic Hypersensitivity Disease 64 0.061
131
P CRN018 Coronary Artery Anomaly 63 0.061
132
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.061
133
P PRD008 Periodontitis 62 0.061
134
P ENC004 Encephalitis 61 0.061
135
CRY005 Cryptococcosis 58 0.061
136
P INF032 Infertility 57 0.061
137
DSS009 Disseminated Intravascular Coagulation 57 0.061
138
BRN012 Bronchiolitis Obliterans 56 0.061
139
c SVR001 Severe Acute Respiratory Syndrome 55 0.061
140
c CNG415 Congenital Disorder of Glycosylation, Type Ia 55 0.061
141
ART140 Arteries, Anomalies of 53 0.061
142
SPN051 Spondylitis 52 0.061
143
BRN071 Brain Injury 49 0.061
144
MSC077 Muscle Eye Brain Disease 47 0.061
145
INF009 Inflammatory Spondylopathy 32 0.061
146
P PRS040 Prostate Cancer 97 0.054
147
P OVR042 Ovarian Cancer 89 0.054
148
MYL069 Myeloma, Multiple 85 0.054
149
P MLT020 Multiple Sclerosis 72 0.054
150
P KDN018 Kidney Disease 70 0.054
151
P HPT021 Hepatitis 67 0.054
152
P LPR021 Leprosy 3 67 0.054
153
P DRM053 Dermatitis, Atopic 66 0.054
155
c MNN047 Mannosidosis, Alpha B, Lysosomal 64 0.054
156
P VSC007 Vascular Disease 63 0.054
157
LYM017 Lyme Disease 63 0.054
158
P CRN300 Coronary Heart Disease 1 63 0.054
159
SKN016 Skin Disease 63 0.054
160
HYP066 Hyperglycemia 61 0.054
161
ACQ007 Acquired Immunodeficiency Syndrome 60 0.054
162
CHC001 Chickenpox 60 0.054
163
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 59 0.054
164
THY029 Thyroid Carcinoma 59 0.054
165
BRN056 Bronchopulmonary Dysplasia 57 0.054
166
PLS011 Plasmacytoma 56 0.054
167
AVN001 Avian Influenza 56 0.054
168
PRN019 Perinatal Necrotizing Enterocolitis 54 0.054
169
CRY003 Cryptosporidiosis 54 0.054
170
PRC002 Paracoccidioidomycosis 53 0.054
171
CCC001 Coccidioidomycosis 53 0.054
172
TRM010 Traumatic Brain Injury 53 0.054
173
BCT002 Bacterial Vaginosis 52 0.054
174
P ECL001 Eclampsia 51 0.054
175
P OVR082 Overgrowth Syndrome 50 0.054
176
NTR046 Neutrophil Migration 50 0.054
177
MNN009 Meningoencephalitis 49 0.054
178
c INV001 Invasive Aspergillosis 48 0.054
179
RNL077 Renal Fibrosis 47 0.054
180
c INH020 Inherited Metabolic Disorder 46 0.054
181
IMM003 Immunoglobulin Alpha Deficiency 45 0.054
182
CRB004 Cerebral Artery Occlusion 44 0.054
183
PNM013 Pneumococcal Meningitis 43 0.054
184
CRN319 Coronavirus Infection 38 0.054
185
HNS001 Hansen's Disease 34 0.054
186
PLY150 Polykaryocytosis Inducer 31 0.054
187
PHS025 Phosphatase, Acid, of Tissues 28 0.054
188
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.047
189
P ALZ034 Alzheimer Disease 88 0.047
190
c LKM061 Leukemia, Acute Myeloid 83 0.047
191
INS024 Insulin-Like Growth Factor I 79 0.047
192
CRV035 Cervical Cancer 76 0.047
193
P RSP003 Respiratory Failure 74 0.047
194
ULC004 Ulcerative Colitis 73 0.047
195
c THR092 Thrombophilia Due to Thrombin Defect 73 0.047
196
P GRF003 Graft-Versus-Host Disease 71 0.047
197
PRP027 Peripheral Vascular Disease 71 0.047
198
FBR012 Fabry Disease 71 0.047
199
P NRB001 Neuroblastoma 71 0.047
200
P SRC025 Sarcoidosis 1 70 0.047
201
P MYC007 Myocardial Infarction 70 0.047
202
P PRM011 Primary Ciliary Dyskinesia 69 0.047
203
P CLC063 Celiac Disease 1 68 0.047
204
LKC009 Leukocyte Adhesion Deficiency, Type I 67 0.047
205
OST159 Osteogenic Sarcoma 66 0.047
206
LPT001 Leptospirosis 66 0.047
207
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.047
208
TTN003 Tetanus 64 0.047
209
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.047
210
P END044 Endometriosis 62 0.047
211
P DRM010 Dermatomyositis 61 0.047
212
NTR005 Nutritional Deficiency Disease 61 0.047
213
DRM006 Dermatitis 61 0.047
214
DPH001 Diphtheria 60 0.047
215
P NMN002 Niemann-Pick Disease 60 0.047
216
DNG002 Dengue Hemorrhagic Fever 60 0.047
217
P MYC008 Myocarditis 59 0.047
218
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 59 0.047
219
P TRC086 Trichohepatoenteric Syndrome 1 59 0.047
220
IGR001 Ige Responsiveness, Atopic 59 0.047
221
P FCL005 Focal Segmental Glomerulosclerosis 58 0.047
222
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.047
223
c ACT073 Acute Leukemia 58 0.047
224
LYM027 Lymphopenia 57 0.047
225
EMB004 Embryonal Carcinoma 57 0.047
226
GST033 Gestational Diabetes 57 0.047
227
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.047
228
ERY051 Erythroleukemia, Familial 56 0.047
229
P MYS005 Myositis 56 0.047
230
PRP030 Purpura 55 0.047
231
c BCT007 Bacterial Meningitis 55 0.047
232
PLM010 Pulmonary Edema 55 0.047
233
P LFT003 Left Ventricular Noncompaction 55 0.047
234
HYP060 Hyperinsulinism 54 0.047
235
PNM001 Pneumocystosis 54 0.047
236
RHM028 Rheumatic Heart Disease 53 0.047
237
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.047
238
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.047
239
P END047 Endophthalmitis 52 0.047
240
PLS009 Plasma Cell Neoplasm 51 0.047
241
BWN001 Bowen-Conradi Syndrome 51 0.047
242
P MMB011 Membranous Nephropathy 50 0.047
243
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.047
244
P IGN003 Iga Nephropathy 1 49 0.047
245
BNR002 Bone Resorption Disease 48 0.047
246
CRY014 Cryptococcal Meningitis 48 0.047
247
SPL018 Splenomegaly 48 0.047
248
c CNG206 Congenital Disorder of Glycosylation, Type Ie 47 0.047
249
TRT001 Teratocarcinoma 46 0.047
250
c ACT042 Acute Pyelonephritis 44 0.047
251
P BCT020 Bacteremia 2 44 0.047
252
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.047
253
P CRN024 Corneal Disease 43 0.047
254
c CHR682 Chronic Bilirubin Encephalopathy 38 0.047
255
CND006 Candida Glabrata 32 0.047
256
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.047
257
AMB007 Amoebic Keratitis 20 0.047
259
c DLT002 Dilated Cardiomyopathy 79 0.039
260
P LNG064 Lung Cancer Susceptibility 3 77 0.039
261
P HRT032 Heart Disease 75 0.039
262
KPS004 Kaposi Sarcoma 75 0.039
263
c ATR087 Atrial Standstill 1 74 0.039
264
SCK003 Sickle Cell Anemia 72 0.039
265
c HYP836 Hypercholesterolemia, Familial, 1 72 0.039
266
P AMY004 Amyloidosis 70 0.039
267
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.039
268
ADL002 Adult Syndrome 69 0.039
269
P MYS003 Myasthenia Gravis 68 0.039
270
CRB037 Cerebral Palsy 68 0.039
271
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.039
272
c CHR684 Chronic Kidney Disease 66 0.039
273
AND002 Androgen Insensitivity Syndrome 66 0.039
274
P AGM001 Agammaglobulinemia 65 0.039
275
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.039
276
BRR014 Barrett Esophagus 64 0.039
277
OST017 Osteomyelitis 64 0.039
278
NRF007 Neurofibroma 64 0.039
279
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.039
280
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.039
281
P ANR048 Aniridia 1 63 0.039
282
ANR007 Anorexia Nervosa 63 0.039
283
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.039
284
LPD008 Lipid Metabolism Disorder 62 0.039
285
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.039
286
CTN007 Cutaneous Leishmaniasis 61 0.039
287
CHR066 Chronic Fatigue Syndrome 61 0.039
288
FTT001 Fatty Liver Disease 61 0.039
289
BRC012 Brucellosis 61 0.039
290
LGN002 Legionellosis 61 0.039
291
c HRD002 Hereditary Angioedema 61 0.039
292
P PNC044 Pancreatitis 61 0.039
293
PRT013 Portal Hypertension 60 0.039
294
ACN002 Acanthosis Nigricans 60 0.039
295
P MYL006 Myeloid Leukemia 60 0.039
296
INS001 Insulinoma 60 0.039
297
SQM006 Squamous Cell Carcinoma 60 0.039
298
P GLL022 Guillain-Barre Syndrome 59 0.039
299
P GLY013 Glycogen Storage Disease 59 0.039
300
P ECT006 Ectodermal Dysplasia 59 0.039
301
c ACT027 Acute Pancreatitis 59 0.039
302
c ACT071 Acute Kidney Failure 59 0.039
303
ADN018 Adenoma 58 0.039
304
P AXN002 Axenfeld-Rieger Syndrome 58 0.039
305
P END033 Endocarditis 57 0.039
306
THR024 Thrombosis 56 0.039
307
P CHN012 Chondrosarcoma 56 0.039
308
AGN016 Aging 56 0.039
309
P MLN007 Male Infertility 56 0.039
310
SYN007 Synovitis 55 0.039
311
MCS002 Mucositis 55 0.039
312
P MLT074 Multiple Endocrine Neoplasia 55 0.039
313
WST005 West Nile Virus 55 0.039
314
VGN023 Vaginitis 55 0.039
315
P ANT006 Antiphospholipid Syndrome 54 0.039
316
P LCH002 Lichen Planus 54 0.039
317
P ANG015 Angioedema 54 0.039
318
JPN002 Japanese Encephalitis 54 0.039
319
GLC003 Glucose Intolerance 54 0.039
320
c PRD040 Periodontitis, Chronic 54 0.039
321
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.039
322
PRT082 Preterm Premature Rupture of the Membranes 54 0.039
323
MST005 Mastitis 53 0.039
324
P ART018 Aortic Valve Insufficiency 53 0.039
325
THR013 Thoracic Outlet Syndrome 53 0.039
326
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.039
327
PLS007 Plasmodium Falciparum Malaria 52 0.039
328
P INT068 Intestinal Disease 52 0.039
329
DMY004 Demyelinating Disease 52 0.039
330
INF034 Infective Endocarditis 52 0.039
331
OCL069 Ocular Motor Apraxia 51 0.039
332
P LRY019 Laryngitis 51 0.039
333
CHR005 Chorioamnionitis 51 0.039
334
c VRL010 Viral Hepatitis 51 0.039
335
STR008 Strongyloidiasis 51 0.039
336
PLR008 Pleurisy 51 0.039
337
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.039
338
PLC008 Placenta Disease 49 0.039
339
c SVR005 Severe Pre-Eclampsia 49 0.039
340
END021 Endomyocardial Fibrosis 48 0.039
341
SPR010 Sporotrichosis 48 0.039
342
c LRG017 Large Intestine Cancer 47 0.039
343
CHR074 Choriocarcinoma 46 0.039
344
3MC003 3mc Syndrome 46 0.039
345
ORL013 Oral Lichen Planus 45 0.039
346
GRN017 Granulocytopenia 44 0.039
347
DWR001 Dwarfism 44 0.039
348
CRD043 Ceroid Storage Disease 43 0.039
349
c PCH010 Pachyonychia Congenita 3 43 0.039
350
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.039
351
FSC002 Fascioliasis 41 0.039
352
CMP009 Complement Deficiency 40 0.039
353
VLV042 Vulvar Vestibulitis Syndrome 40 0.039
354
P PRG092 Pregnancy Loss, Recurrent 1 40 0.039
355
GLM044 Glomerular Disease 39 0.039
356
c MSC098 Muscular Dystrophy-Dystroglycanopathy , Type C, 14 39 0.039
357
c CNG194 Congenital Disorder of Glycosylation, Type Ig 39 0.039
358
c OVR114 Ovarian Cancer 1 38 0.039
359
OVR094 Ovarian Epithelial Cancer 38 0.039
360
c SYS043 Systemic Lupus Erythematosus 1 38 0.039
361
ATX010 Ataxia Neuropathy Spectrum 38 0.039
362
MNN021 Meningococcemia 37 0.039
363
MYC017 Mycobacterium Kansasii 37 0.039
364
HRW001 Hair Whorl 36 0.039
365
c CNG196 Congenital Disorder of Glycosylation, Type Ic 35 0.039
366
INC022 Inclusion-Cell Disease 35 0.039
367
ALR002 Al-Raqad Syndrome 34 0.039
368
c PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 34 0.039
369
ACT064 Acute Necrotizing Encephalitis 32 0.039
370
CMP064 Complement Component 3 Deficiency 32 0.039
371
c ADL027 Adult Dermatomyositis 30 0.039
372
MCL022 Mucolipidoses 30 0.039
373
c MSC182 Muscular Dystrophy-Dystroglycanopathy , Type C, 15 30 0.039
374
MYC088 Mycobacterium Avium Complex Infections 29 0.039
375
MYC019 Mycobacterium Marinum 29 0.039
376
AND005 Androgen Insensitivity Syndrome, Mild 22 0.039
377
BLD137 Blood Group--Ahonen 19 0.039
378
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.039
379
ARB003 Arbovirosis 15 0.039
380
ESP021 Esophageal Cancer 90 0.027
381
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.027
382
STR067 Stroke, Ischemic 80 0.027
383
c LKM071 Leukemia, Chronic Lymphocytic 79 0.027
384
PFF001 Pfeiffer Syndrome 79 0.027
385
CNN003 Conn's Syndrome 79 0.027
386
OST012 Osteoarthritis 78 0.027
387
P NRF023 Neurofibromatosis, Type Ii 76 0.027
388
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.027
389
GLB015 Glioblastoma Multiforme 75 0.027
390
BRN028 Brain Cancer 73 0.027
391
SVR004 Severe Combined Immunodeficiency 73 0.027
392
P OST002 Osteoporosis 73 0.027
393
MSC157 Muscular Dystrophy, Duchenne Type 71 0.027
394
P PHC003 Pheochromocytoma 71 0.027
395
ACR007 Acromegaly 71 0.027
396
WLS001 Wilson Disease 70 0.027
397
P MTC003 Metachromatic Leukodystrophy 70 0.027
398
DWN001 Down Syndrome 70 0.027
399
MYL009 Myelodysplastic Syndrome 70 0.027
400
BRT054 Brittle Bone Disorder 70 0.027
401
P SYS005 Systemic Scleroderma 70 0.027
402
P TTR001 Tetralogy of Fallot 69 0.027
403
LYM133 Lymphoma, Hodgkin, Classic 69 0.027
404
CRT072 Creutzfeldt-Jakob Disease 69 0.027
405
CRB039 Cerebrovascular Disease 69 0.027
406
P HYP086 Hypothyroidism 68 0.027
407
c BSL007 Basal Cell Carcinoma 68 0.027
408
P LYM118 Lymphoma 68 0.027
409
OBS002 Obsessive-Compulsive Disorder 68 0.027
410
P ALP004 Alport Syndrome 68 0.027
411
c NMN015 Niemann-Pick Disease, Type C1 68 0.027
412
P CHR012 Chronic Granulomatous Disease 67 0.027
413
PNC129 Pancreatic Adenocarcinoma 67 0.027
414
BRK010 Burkitt Lymphoma 67 0.027
415
P TMP003 Temporal Arteritis 67 0.027
416
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.027
417
CHL065 Cholangiocarcinoma 67 0.027
418
ALL003 Allergic Rhinitis 67 0.027
419
P NSP012 Nasopharyngeal Carcinoma 67 0.027
420
P ANG001 Angelman Syndrome 67 0.027
421
P SKN015 Skin Carcinoma 67 0.027
422
PSY004 Psychotic Disorder 67 0.027
423
ANG054 Angina Pectoris 66 0.027
424
SRC014 Sarcoma 65 0.027
425
c HMP029 Hemophilia a 65 0.027
426
P DYS154 Dystonia 65 0.027
427
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.027
428
P THY023 Thymoma 65 0.027
429
P PRS038 Personality Disorder 65 0.027
430
P EPD009 Epidermolysis Bullosa Dystrophica 64 0.027
431
P DBT009 Diabetes Mellitus 64 0.027
432
CLF027 Cleft Palate, Isolated 64 0.027
433
LYS012 Lysosomal Acid Lipase Deficiency 64 0.027
434
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.027
435
MSC007 Muscle Hypertrophy 63 0.027
436
NRM005 Neuromuscular Disease 63 0.027
437
P ADL010 Adult Respiratory Distress Syndrome 63 0.027
438
WLK001 Walker-Warburg Syndrome 63 0.027
439
PPL049 Papillon-Lefevre Syndrome 63 0.027
440
c HPT003 Hepatitis a 63 0.027
441
c SCL052 Scleroderma, Familial Progressive 62 0.027
442
P RHB003 Rhabdomyosarcoma 62 0.027
443
BRS099 Breast Ductal Carcinoma 62 0.027
444
P HML002 Hemolytic Anemia 62 0.027
445
c NMN013 Niemann-Pick Disease, Type a 62 0.027
446
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.027
447
CLT003 Colitis 62 0.027
448
P PSR002 Psoriasis 62 0.027
449
c WLM018 Wilms Tumor 5 62 0.027
450
c GLC092 Glaucoma, Primary Open Angle 62 0.027
451
PSR001 Psoriatic Arthritis 62 0.027
452
ALC006 Alcoholic Hepatitis 61 0.027
453
P PRM006 Primary Biliary Cirrhosis 61 0.027
454
P HMN010 Hemangioma 61 0.027
455
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.027
456
P CTR002 Cataract 60 0.027
457
RCT015 Reactive Arthritis 60 0.027
458
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.027
459
P PTN014 Patent Ductus Arteriosus 1 60 0.027
460
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.027
461
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.027
462
INT066 Interstitial Lung Disease 59 0.027
463
CLS005 Clouston Syndrome 59 0.027
464
P LKD001 Leukodystrophy 59 0.027
465
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.027
466
DCT002 Ductal Carcinoma in Situ 59 0.027
467
PLM033 Pulmonary Embolism 59 0.027
468
HLC007 Helicobacter Pylori Infection 59 0.027
469
P PLV020 Pelvic Organ Prolapse 59 0.027
470
ANR040 Aneurysm 58 0.027
471
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.027
472
P SZR006 Seizure Disorder 58 0.027
473
THY122 Thyroid Gland Cancer 58 0.027
474
P BCL017 B-Cell Lymphoma 58 0.027
475
VSL002 Visual Epilepsy 58 0.027
476
QFV001 Q Fever 58 0.027
477
LYM021 Lymphadenitis 58 0.027
478
CNS004 Constipation 57 0.027
479
P OST122 Osteogenesis Imperfecta, Type Iii 57 0.027
480
P RHN004 Rhinitis 57 0.027
481
P UVT001 Uveitis 57 0.027
482
TNS005 Tonsillitis 57 0.027
483
P SHR029 Short Syndrome 57 0.027
484
APH001 Aphthous Stomatitis 57 0.027
485
c ANG068 Angioedema, Hereditary, Type I 56 0.027
486
P FBR017 Fibrosarcoma 56 0.027
487
c ACT075 Acute Myocardial Infarction 56 0.027
488
P ALP008 Alopecia 56 0.027
489
P PLY011 Polycystic Ovary Syndrome 56 0.027
490
CMM005 Common Cold 56 0.027
491
RHM027 Rheumatic Disease 56 0.027
492
ALL006 Allergic Asthma 56 0.027
493
HMG005 Hemoglobinopathy 55 0.027
494
P GST044 Gastritis 55 0.027
495
P PNM006 Pneumoconiosis 55 0.027
496
HYP005 Hypokalemia 55 0.027
497
c MCL046 Mucolipidosis Iii Alpha/beta 55 0.027
498
P BRT004 Bartter Disease 55 0.027
499
c GRV008 Graves Disease 1 55 0.027
500
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.027
501
FLR002 Filariasis 55 0.027
502
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.027
503
INT007 Intermediate Coronary Syndrome 55 0.027
504
FCT001 Factor Viii Deficiency 55 0.027
505
DBT010 Diabetic Neuropathy 55 0.027
506
CLL003 Cellulitis 54 0.027
507
c MCP043 Mucopolysaccharidosis, Type Iiia 54 0.027
508
LST001 Listeriosis 54 0.027
509
LYM040 Lymphoblastic Lymphoma 54 0.027
510
AMN001 Amenorrhea 54 0.027
511
c THY107 Thymoma, Familial 54 0.027
512
CYS005 Cysticercosis 54 0.027
513
HLL004 Hellp Syndrome 53 0.027
514
CHK001 Chikungunya 53 0.027
515
P EPD016 Epidermolysis Bullosa 53 0.027
516
RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.027
517
HRT012 Heart Valve Disease 53 0.027
518
MMB001 Membranoproliferative Glomerulonephritis 53 0.027
519
LYM022 Lymphangioma 53 0.027
520
CRH005 Crohn's Colitis 52 0.027
521
P CTN003 Cutaneous Lupus Erythematosus 52 0.027
522
P PTS002 Ptosis 52 0.027
523
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.027
524
PST011 Pustulosis of Palm and Sole 52 0.027
525
P HML001 Hemolytic-Uremic Syndrome 52 0.027
526
STT041 Stuttering 52 0.027
527
P INS002 in Situ Carcinoma 52 0.027
528
CHR073 Choreatic Disease 52 0.027
529
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.027
530
THY124 Thyroid Gland Papillary Carcinoma 52 0.027
531
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.027
532
PRV004 Periventricular Leukomalacia 51 0.027
533
P HMP007 Hemophilia 51 0.027
534
c ACT135 Acute Graft Versus Host Disease 51 0.027
535
OVR059 Ovary Adenocarcinoma 51 0.027
536
MSC190 Muscular Disease 51 0.027
537
DNT012 Dental Caries 51 0.027
538
GNG012 Gingival Overgrowth 51 0.027
539
P MNN019 Mannosidosis, Beta a, Lysosomal 51 0.027
540
c ACT134 Acute Liver Failure 51 0.027
541
SCB001 Scabies 51 0.027
542
SPN035 Spindle Cell Sarcoma 51 0.027
543
c CNG191 Congenital Disorder of Glycosylation, Type Iia 50 0.027
544
HYP081 Hypolipoproteinemia 50 0.027
545
P ATR005 Atrophic Gastritis 50 0.027
546
P THR015 Thrombophilia 50 0.027
547
LGN006 Legionnaire Disease 50 0.027
548
c GCH016 Gaucher Disease, Type Ii 50 0.027
549
CHL061 Childhood Leukemia 50 0.027
550
INT079 Intrahepatic Cholangiocarcinoma 50 0.027
551
FLR001 Filarial Elephantiasis 50 0.027
552
CRT013 Carotid Stenosis 50 0.027
553
P DDN001 Duodenal Ulcer 50 0.027
554
c AMY009 Amyloidosis Aa 50 0.027
555
TRY001 Trypanosomiasis 50 0.027
556
c MLG054 Malignant Histiocytosis 50 0.027
557
PLR001 Pleural Tuberculosis 50 0.027
558
HRP009 Herpes Simplex Encephalitis 50 0.027
559
TLR001 Tularemia 49 0.027
560
c VRL005 Viral Pneumonia 49 0.027
561
VRC001 Varicocele 49 0.027
562
FDL002 Food Allergy 49 0.027
563
PLR007 Pleural Empyema 49 0.027
564
P OPN001 Open-Angle Glaucoma 49 0.027
565
LFT001 Left Bundle Branch Hemiblock 49 0.027
566
BLL003 Bell's Palsy 49 0.027
567
BLS002 Blastomycosis 49 0.027
568
HMG002 Hemoglobinuria 49 0.027
569
ECT026 Ectopic Pregnancy 49 0.027
570
URM002 Uremia 49 0.027
571
SLP001 Sleeping Sickness 48 0.027
572
DYN002 Doyne Honeycomb Retinal Dystrophy 48 0.027
573
c MSC035 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 48 0.027
574
CRD137 Cardiogenic Shock 48 0.027
575
TBR011 Tuberculous Meningitis 48 0.027
576
FCL012 Facial Paralysis 48 0.027
577
P RNL015 Renal Hypertension 48 0.027
578
BNN003 Bone Inflammation Disease 48 0.027
579
ANT018 Anthracosis 48 0.027
580
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.027
581
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.027
582
PRP007 Priapism 48 0.027
583
LPD004 Lipoid Nephrosis 47 0.027
584
c MSC042 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 47 0.027
585
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.027
586
P END046 Endometritis 47 0.027
587
PPL002 Papillary Carcinoma 47 0.027
588
c BCT013 Bacterial Pneumonia 47 0.027
589
TTR011 Tetraploidy 47 0.027
590
P TCL004 T-Cell Leukemia 47 0.027
591
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.027
592
LYM019 Lymphosarcoma 47 0.027
593
MCC002 Mucocutaneous Leishmaniasis 47 0.027
594
PLS025 Plasmablastic Lymphoma 47 0.027
595
MCL009 Mcleod Syndrome 47 0.027
596
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.027
597
RTN001 Retinal Vasculitis 46 0.027
598
LYM009 Lymphocytic Choriomeningitis 46 0.027
599
OLG020 Oligoarticular Juvenile Idiopathic Arthritis 46 0.027
600
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.027
601
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.027
602
ADR040 Adrenal Gland Pheochromocytoma 46 0.027
603
URT010 Ureteral Obstruction 46 0.027
604
FLL008 Folliculitis 46 0.027
605
EXT033 Extrapulmonary Tuberculosis 46 0.027
606
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.027
607
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.027
608
c MLG068 Malignant Glioma 45 0.027
609
STR103 Streptococcus Pneumonia 45 0.027
610
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.027
611
SPP008 Suppurative Otitis Media 45 0.027
612
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.027
613
MNN020 Meningococcal Infection 45 0.027
614
LYM051 Lymphomatoid Granulomatosis 45 0.027
615
PTT037 Pituitary Tumors 44 0.027
616
c MSC093 Muscular Dystrophy-Dystroglycanopathy , Type C, 3 44 0.027
617
CTY001 Cat Eye Syndrome 44 0.027
618
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.027
619
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.027
620
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.027
621
P GNG009 Gangliosidosis 44 0.027
622
CLN003 Clonorchiasis 43 0.027
623
BRN032 Brain Glioma 43 0.027
624
LTH001 Lethal Midline Granuloma 43 0.027
625
c MCL016 Mucolipidosis Iii Gamma 43 0.027
626
CMP007 Complement Component 5 Deficiency 43 0.027
627
CRS001 Crescentic Glomerulonephritis 43 0.027
628
c PRM038 Primary Agammaglobulinemia 43 0.027
629
DYS018 Dysostosis 43 0.027
630
DNG001 Dengue Shock Syndrome 43 0.027
631
LWC001 Low Compliance Bladder 42 0.027
632
DSC009 Discoid Lupus Erythematosus 42 0.027
633
PRS036 Parasitic Protozoa Infectious Disease 42 0.027
634
P CLL015 Collagen Disease 42 0.027
635
PRS115 Prosthetic Joint Infection 42 0.027
636
TRP014 Triploidy 42 0.027
637
c HYP072 Hypersensitivity Reaction Type Iii Disease 42 0.027
638
P HYP265 Hypotonia 42 0.027
639
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.027
640
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.027
641
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 40 0.027
642
C1N001 C1 Inhibitor Deficiency 40 0.027
643
c MYC083 Myoclonic Epilepsy, Familial Infantile 39 0.027
644
IMM001 Immune-Complex Glomerulonephritis 39 0.027
645
CRV045 Cervical Intraepithelial Neoplasia 39 0.027
646
BRC011 Brachial Plexus Neuropathy 39 0.027
648
HMR023 Hemorrhagic Cystitis 38 0.027
649
c ATM075 Autoimmune Encephalitis 38 0.027
650
ESN006 Eosinophilic Meningitis 38 0.027
651
MCP033 Mucopolysaccharidoses 38 0.027
652
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 37 0.027
653
P CNG048 Congenital Hepatic Fibrosis 37 0.027
654
PNB004 Panbronchiolitis, Diffuse 37 0.027
655
SYS071 Systemic Autoimmune Disease 37 0.027
656
P MSC002 Muscular Dystrophy-Dystroglycanopathy 35 0.027
657
c CNG192 Congenital Disorder of Glycosylation, Type Ik 35 0.027
658
GNT033 Genetic Prion Diseases 35 0.027
659
c CNG386 Congenital Disorder of Glycosylation, Type Iu 35 0.027
660
GLY058 Glycogen Storage Disease 0, Liver 34 0.027
661
GNG006 Gingival Hypertrophy 34 0.027
662
HMN016 Hemangioendothelioma 34 0.027
663
PRG090 Progressive Relapsing Multiple Sclerosis 34 0.027
664
c SBC035 Subacute Cutaneous Lupus Erythematosus 33 0.027
665
CMP040 Complement Component 4, Partial Deficiency of 33 0.027
666
INF013 Inferior Myocardial Infarction 33 0.027
667
MTB016 Metabolic Myopathy 33 0.027
668
ACD003 Acid Sphingomyelinase Deficiency 32 0.027
669
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 32 0.027
670
MYC014 Mycobacterium Chelonae 32 0.027
671
c CHR097 Chronic Purulent Otitis Media 32 0.027
672
c GLY043 Glycogen Storage Disease Xii 31 0.027
673
P RRL003 Rare Lymphatic Malformation 31 0.027
674
MYC015 Mycobacterium Fortuitum 31 0.027
675
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 31 0.027
676
PRM004 Primary Amebic Meningoencephalitis 31 0.027
677
PLX004 Plexopathy 30 0.027
678
PRP038 Properdin Deficiency, X-Linked 30 0.027
679
GRV012 Grover's Disease 30 0.027
680
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.027
681
PLM007 Pulmonary Aspergilloma 28 0.027
682
ARG004 Argyria 28 0.027
683
c GLY023 Glycogen Storage Disease Type 0 27 0.027
684
c MSC099 Muscular Dystrophy-Dystroglycanopathy , Type B, 14 27 0.027
685
CHL079 Children's Interstitial Lung Disease 27 0.027
686
c MSC097 Muscular Dystrophy-Dystroglycanopathy , Type a, 14 27 0.027
687
ACT181 Acute Motor Axonal Neuropathy 26 0.027
688
LYS030 Lysosomal Storage Disease with Skeletal Involvement 25 0.027
689
HRP008 Herpes Simiae 25 0.027
690
c IGN004 Iga Nephropathy 3 25 0.027
691
MSP001 Masp2 Deficiency 25 0.027
692
PLY179 Polyomavirus-Associated Nephropathy 23 0.027
693
c GLC079 Glaucoma 1, Open Angle, P 23 0.027
694
c BKV001 Bk-Virus Nephropathy 23 0.027
695
c CNG507 Congenital Disorder of Glycosylation, Type I/iix 23 0.027
696
c FCL082 Focal Segmental Glomerulosclerosis 4 22 0.027
697
SHR119 Short Stature, Amelogenesis Imperfecta, and Skeletal Dysplasia with Scoliosis 21 0.027
698
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 21 0.027
699
PRP033 Properdin Deficiency 15 0.027
700
SCR040 Secretory Component Deficiency 15 0.027
701
CMP031 Complement Component Deficiency 12 0.027
Content
Loading form....