Search results for NAD

534 hits were found for NAD

# Family MCID Name MIFTS Score
1
P HYP769 Hyperlysinemia, Type I 41 3.783
2
P VRT014 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1 24 3.126
3
NTR027 Neutrophil Actin Dysfunction 24 3.112
4
CNG532 Congenital Vertebral-Cardiac-Renal Anomalies Syndrome 17 3.075
5
SJG002 Sjogren-Larsson Syndrome 54 2.264
6
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 19 2.236
7
P ENC069 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 1 25 2.220
8
c ENC066 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 2 24 2.200
9
c VRT017 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 3 16 2.200
10
DPH001 Diphtheria 60 0.205
11
PRT037 Pertussis 65 0.183
12
AGN016 Aging 56 0.183
13
P LNG032 Lung Cancer 98 0.164
14
P CLR023 Colorectal Cancer 99 0.151
15
FTT001 Fatty Liver Disease 61 0.151
16
P VSC007 Vascular Disease 63 0.148
17
CHL014 Cholera 59 0.148
18
HMP009 Haemophilus Influenzae 43 0.131
19
P PNC035 Pancreatic Cancer 84 0.120
20
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.120
21
HYP066 Hyperglycemia 61 0.120
22
ISC004 Ischemia 58 0.120
23
c MCR113 Microvascular Complications of Diabetes 3 52 0.120
24
c MCR120 Microvascular Complications of Diabetes 7 47 0.120
25
c MCR130 Microvascular Complications of Diabetes 6 41 0.120
26
c MCR133 Microvascular Complications of Diabetes 4 41 0.120
27
WLL004 Wallerian Degeneration 39 0.120
28
P BRS047 Breast Cancer 97 0.116
29
c HYP836 Hypercholesterolemia, Familial, 1 73 0.116
30
P ALZ034 Alzheimer Disease 88 0.111
31
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.107
32
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.102
33
HPT022 Hepatoblastoma 56 0.102
34
HLX001 Helix Syndrome 47 0.102
35
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.102
36
P LKM002 Leukemia 68 0.098
37
BRN071 Brain Injury 49 0.098
38
P HPT023 Hepatocellular Carcinoma 100 0.093
39
P BLD134 Bladder Cancer 79 0.093
40
P HNT016 Huntington Disease 72 0.093
41
P NRB001 Neuroblastoma 72 0.093
42
P LKM062 Leukemia, Acute Lymphoblastic 69 0.093
43
P LVR013 Liver Disease 68 0.093
44
P MYC084 Mycobacterium Tuberculosis 1 68 0.093
45
ATH013 Atherosclerosis Susceptibility 65 0.093
46
ART002 Arts Syndrome 64 0.093
47
HYP266 Hypoxia 57 0.093
48
CRB004 Cerebral Artery Occlusion 45 0.093
49
ANX004 Anoxia 40 0.093
50
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.087
51
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.087
52
P PRP019 Peripheral Nervous System Disease 58 0.087
53
P MTC069 Mitochondrial Disorders 56 0.087
54
P NRP001 Neuropathy 56 0.087
55
P LTR001 Lateral Sclerosis 54 0.087
56
TRM010 Traumatic Brain Injury 51 0.087
57
PRM329 Premature Aging 35 0.087
58
MYL069 Myeloma, Multiple 85 0.082
59
c LKM061 Leukemia, Acute Myeloid 84 0.082
60
GLB015 Glioblastoma Multiforme 75 0.082
61
P ADN016 Adenocarcinoma 64 0.082
62
P MYL006 Myeloid Leukemia 60 0.082
63
ALL014 Allergic Encephalomyelitis 38 0.082
64
P PRS040 Prostate Cancer 97 0.076
65
ESP021 Esophageal Cancer 90 0.076
66
P LNG064 Lung Cancer Susceptibility 3 78 0.076
67
P HRT032 Heart Disease 75 0.076
68
P MYP004 Myopathy 70 0.076
69
P SKN015 Skin Carcinoma 66 0.076
70
P CCK001 Cockayne Syndrome 66 0.076
71
c SML038 Small Cell Cancer of the Lung 65 0.076
72
LPD008 Lipid Metabolism Disorder 62 0.076
73
PHR003 Pharyngitis 57 0.076
74
CND006 Candida Glabrata 32 0.076
75
P ATX030 Ataxia-Telangiectasia 82 0.069
76
CRV035 Cervical Cancer 76 0.069
77
END057 Endometrial Cancer 74 0.069
78
CNG034 Congestive Heart Failure 69 0.069
79
P MLN008 Melanoma 69 0.069
80
BRK010 Burkitt Lymphoma 67 0.069
81
P MSC005 Muscular Dystrophy 66 0.069
82
P MCR115 Microvascular Complications of Diabetes 5 66 0.069
83
P PLM036 Pulmonary Fibrosis 65 0.069
84
P GLM045 Glioma 63 0.069
85
P CRN300 Coronary Heart Disease 1 63 0.069
86
ATM095 Autoimmune Disease 62 0.069
87
P BRS044 Breast Adenocarcinoma 59 0.069
88
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.069
89
P RTN016 Retinal Degeneration 53 0.069
90
TLN003 Telangiectasis 52 0.069
91
FSC004 Fasciitis 50 0.069
92
47X002 47,xyy 49 0.069
93
MTC005 Mitochondrial Metabolism Disease 49 0.069
94
NCR007 Necrotizing Fasciitis 48 0.069
95
GLL048 Glial Tumor 45 0.069
96
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.069
97
P OVR042 Ovarian Cancer 88 0.062
98
P LKM071 Leukemia, Chronic Lymphocytic 79 0.062
99
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.062
100
P CHR012 Chronic Granulomatous Disease 67 0.062
101
OST159 Osteogenic Sarcoma 66 0.062
102
CHG001 Chagas Disease 66 0.062
103
CLN015 Colon Adenocarcinoma 65 0.062
104
MSC007 Muscle Hypertrophy 64 0.062
105
LSH001 Leishmaniasis 63 0.062
106
ACT119 Acute Promyelocytic Leukemia 63 0.062
107
LPP008 Lipoprotein Quantitative Trait Locus 62 0.062
108
TXC005 Toxic Shock Syndrome 62 0.062
109
SQM006 Squamous Cell Carcinoma 60 0.062
110
P FBR017 Fibrosarcoma 56 0.062
111
GLC003 Glucose Intolerance 54 0.062
112
P SPP010 Suppressor of Tumorigenicity 3 51 0.062
113
P MTC133 Mitochondrial Myopathy 49 0.062
114
ATS010 Autosomal Recessive Disease 48 0.062
115
LYM019 Lymphosarcoma 46 0.062
116
P PLL002 Pellagra 46 0.062
117
P KLZ004 Kala-Azar 1 41 0.062
118
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.062
119
STR077 Streptococcal Toxic-Shock Syndrome 37 0.062
120
HRW001 Hair Whorl 36 0.062
121
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.062
122
STN013 Stenotrophomonas Maltophilia Infection 25 0.062
123
P GST053 Gastric Cancer 83 0.054
124
MLR004 Malaria 81 0.054
125
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.054
126
P PRK057 Parkinson Disease, Late-Onset 78 0.054
127
P KDN018 Kidney Disease 72 0.054
128
P MLT020 Multiple Sclerosis 72 0.054
129
c HPT073 Hepatitis C Virus 72 0.054
130
P PHC003 Pheochromocytoma 71 0.054
131
LGH007 Leigh Syndrome 70 0.054
132
P LYM118 Lymphoma 68 0.054
133
CHL065 Cholangiocarcinoma 68 0.054
134
P PLM037 Pulmonary Hypertension 67 0.054
135
P HML002 Hemolytic Anemia 63 0.054
136
P NTR004 Neutropenia 63 0.054
137
TRN015 Transient Cerebral Ischemia 63 0.054
138
CRC021 Carcinosarcoma 62 0.054
139
P SNS001 Sensorineural Hearing Loss 60 0.054
140
THY029 Thyroid Carcinoma 59 0.054
141
APP015 Apparent Mineralocorticoid Excess 58 0.054
142
P GLM007 Glomerulonephritis 57 0.054
143
c ACT075 Acute Myocardial Infarction 57 0.054
144
SCH014 Schistosomiasis 57 0.054
145
P GST044 Gastritis 56 0.054
146
P INF037 Inflammatory Bowel Disease 54 0.054
147
P RTN018 Retinal Disease 53 0.054
148
ART140 Arteries, Anomalies of 52 0.054
149
P LCT001 Lactic Acidosis 51 0.054
150
INT079 Intrahepatic Cholangiocarcinoma 51 0.054
151
LNG031 Lung Benign Neoplasm 51 0.054
152
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.054
153
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 49 0.054
154
ADR040 Adrenal Gland Pheochromocytoma 46 0.054
155
c MLG068 Malignant Glioma 46 0.054
157
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.054
158
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.054
159
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.054
160
PST092 Posttransplant Acute Limbic Encephalitis 29 0.054
161
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.044
163
c HYP595 Hypertension, Essential 84 0.044
164
c FNC027 Fanconi Anemia, Complementation Group a 81 0.044
165
OST012 Osteoarthritis 78 0.044
166
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.044
167
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.044
168
PHN003 Phenylketonuria 75 0.044
169
c ATR087 Atrial Standstill 1 75 0.044
170
P SCH015 Schizophrenia 74 0.044
171
SVR004 Severe Combined Immunodeficiency 73 0.044
172
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.044
173
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.044
174
HMN044 Human Immunodeficiency Virus Type 1 71 0.044
175
c EXD008 Exudative Vitreoretinopathy 1 71 0.044
176
P ATS364 Autism 70 0.044
177
GST040 Gastric Adenocarcinoma 70 0.044
178
MYL009 Myelodysplastic Syndrome 70 0.044
179
c CHR684 Chronic Kidney Disease 70 0.044
180
LYM133 Lymphoma, Hodgkin, Classic 69 0.044
181
PNC129 Pancreatic Adenocarcinoma 68 0.044
182
CRB039 Cerebrovascular Disease 67 0.044
183
P TRN020 Turner Syndrome 67 0.044
184
c ATS007 Autism Spectrum Disorder 67 0.044
185
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.044
186
ANG054 Angina Pectoris 66 0.044
187
LBR036 Leber Plus Disease 66 0.044
188
HYP056 Hypoglycemia 66 0.044
189
P ATR011 Atrial Fibrillation 66 0.044
190
P DRM053 Dermatitis, Atopic 66 0.044
191
BRR014 Barrett Esophagus 65 0.044
192
c DBT099 Diabetes Mellitus, Type I 65 0.044
193
P DBT009 Diabetes Mellitus 64 0.044
194
CLR108 Colorectal Adenoma 64 0.044
195
c PRC016 Pre-Eclampsia 63 0.044
196
DPR016 Depression 63 0.044
197
P END044 Endometriosis 63 0.044
198
HMT002 Hematologic Cancer 62 0.044
199
ALL026 Allergic Hypersensitivity Disease 62 0.044
200
DRM006 Dermatitis 61 0.044
201
P PNC044 Pancreatitis 61 0.044
202
SPN186 Spinal Cord Injury 60 0.044
203
INS001 Insulinoma 60 0.044
204
c ACT071 Acute Kidney Failure 60 0.044
205
P MYC008 Myocarditis 59 0.044
206
CHL123 Chlamydia 59 0.044
207
P CYS018 Cystitis 59 0.044
208
HLC007 Helicobacter Pylori Infection 59 0.044
209
c ACT073 Acute Leukemia 58 0.044
210
P ALC033 Alcohol Use Disorder 58 0.044
211
LYM027 Lymphopenia 58 0.044
212
BRN056 Bronchopulmonary Dysplasia 57 0.044
213
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.044
214
P PRN023 Prion Disease 57 0.044
215
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.044
216
P CRD246 Cardiovascular System Disease 57 0.044
217
P PLY011 Polycystic Ovary Syndrome 56 0.044
218
ERY051 Erythroleukemia, Familial 56 0.044
219
HYP005 Hypokalemia 55 0.044
220
LMB062 Limb Ischemia 55 0.044
221
P DRR001 Diarrhea 55 0.044
222
VSC003 Visceral Leishmaniasis 55 0.044
223
HYP060 Hyperinsulinism 54 0.044
224
TRD006 Tardive Dyskinesia 54 0.044
225
P ICH004 Ichthyosis 54 0.044
226
SLP001 Sleeping Sickness 54 0.044
227
PRS045 Prostatic Hypertrophy 53 0.044
228
HMC014 Homocysteinemia 53 0.044
229
DNT012 Dental Caries 53 0.044
230
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.044
231
P RCT021 Rectum Cancer 52 0.044
232
IMP005 Impotence 52 0.044
233
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.044
234
PRS021 Prostatic Adenoma 51 0.044
235
CHR005 Chorioamnionitis 51 0.044
236
HST006 Histidinemia 48 0.044
237
P RNV001 Renovascular Hypertension 48 0.044
238
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.044
239
ADN009 Adenosquamous Carcinoma 47 0.044
240
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.044
241
CHR074 Choriocarcinoma 47 0.044
242
RTN020 Retinal Vascular Disease 46 0.044
243
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.044
244
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.044
245
HDN002 Head Injury 46 0.044
246
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.044
247
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.044
248
GRN017 Granulocytopenia 44 0.044
249
c SPR086 Spermatogenic Failure 3 44 0.044
250
CVD001 Covid-19 44 0.044
251
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.044
252
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.044
253
CYT002 Cytokine Deficiency 42 0.044
254
HRN029 Hearing Loss, Noise-Induced 37 0.044
255
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.044
256
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 0.044
257
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 34 0.044
258
PPL052 Papillomatosis, Confluent and Reticulated 33 0.044
259
c LNG109 Lung Cancer Susceptibility 1 27 0.044
260
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.044
261
c SYS001 Systemic Lupus Erythematosus 86 0.031
262
c DLT002 Dilated Cardiomyopathy 79 0.031
263
INS024 Insulin-Like Growth Factor I 79 0.031
264
c CWD006 Cowden Syndrome 1 78 0.031
265
AST005 Asthma 76 0.031
266
P APL001 Aplastic Anemia 74 0.031
267
SCK003 Sickle Cell Anemia 74 0.031
268
ULC004 Ulcerative Colitis 73 0.031
269
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.031
270
P CNR004 Cone-Rod Dystrophy 2 73 0.031
271
P GRF003 Graft-Versus-Host Disease 72 0.031
272
P BRG001 Brugada Syndrome 71 0.031
273
DFC004 Deficiency Anemia 70 0.031
274
P HYP061 Hypertrophic Cardiomyopathy 70 0.031
275
WRN001 Werner Syndrome 69 0.031
276
PLM001 Pulmonary Tuberculosis 69 0.031
277
P ART022 Arthritis 69 0.031
278
P HYP086 Hypothyroidism 69 0.031
279
ART016 Aortic Aneurysm 69 0.031
280
P MPL001 Maple Syrup Urine Disease 69 0.031
281
MNT001 Mantle Cell Lymphoma 69 0.031
282
c BSL007 Basal Cell Carcinoma 68 0.031
283
SKN019 Skin Melanoma 68 0.031
284
RCK004 Rickets 68 0.031
285
P MJR001 Major Depressive Disorder 68 0.031
286
P THR014 Thrombocytopenia 67 0.031
287
P CWD010 Cowden Syndrome 67 0.031
288
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.031
289
P HPT021 Hepatitis 67 0.031
290
ALL003 Allergic Rhinitis 67 0.031
291
THY111 Thyroid Carcinoma, Familial Medullary 67 0.031
292
P BLD062 Bile Duct Cancer 67 0.031
293
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.031
294
P LNG028 Long Qt Syndrome 66 0.031
295
ALC007 Alcohol Dependence 66 0.031
296
CHD001 Chediak-Higashi Syndrome 66 0.031
297
P DMN002 Dementia 66 0.031
298
P MNN013 Meningitis 66 0.031
299
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.031
300
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.031
301
P CTS001 Cutis Laxa 65 0.031
302
PRT036 Peritonitis 64 0.031
303
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.031
304
NRM005 Neuromuscular Disease 64 0.031
305
P GLC113 Galactosemia I 64 0.031
306
P FRD001 Friedreich Ataxia 64 0.031
307
P PRD008 Periodontitis 64 0.031
308
PLM031 Poliomyelitis 64 0.031
309
P RHB003 Rhabdomyosarcoma 63 0.031
310
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.031
311
KRN002 Kearns-Sayre Syndrome 63 0.031
312
SKN016 Skin Disease 63 0.031
313
c ACT068 Acute Cystitis 63 0.031
314
c OPT053 Optic Atrophy 1 63 0.031
315
CLT003 Colitis 62 0.031
316
c HPT001 Hepatitis C 62 0.031
317
P PSR002 Psoriasis 62 0.031
318
c SVR001 Severe Acute Respiratory Syndrome 62 0.031
319
P HYP750 Hypertriglyceridemia, Familial 62 0.031
320
P ESP024 Esophagitis 62 0.031
321
LSC001 Lesch-Nyhan Syndrome 62 0.031
322
P PRM006 Primary Biliary Cirrhosis 62 0.031
323
MSL001 Measles 62 0.031
324
NTR005 Nutritional Deficiency Disease 62 0.031
325
CHL068 Cholestasis 61 0.031
326
P INT143 Interstitial Cystitis 61 0.031
327
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.031
328
c SCL052 Scleroderma, Familial Progressive 61 0.031
329
ALC006 Alcoholic Hepatitis 61 0.031
330
RTN017 Retinal Detachment 61 0.031
331
P LPS004 Lupus Erythematosus 61 0.031
332
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.031
333
P KDN017 Kidney Cancer 60 0.031
334
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.031
335
INT066 Interstitial Lung Disease 60 0.031
336
c ACT027 Acute Pancreatitis 60 0.031
337
CRD223 Cardiac Arrhythmia 60 0.031
338
ACQ007 Acquired Immunodeficiency Syndrome 60 0.031
339
LNG099 Lung Disease 60 0.031
340
RHM001 Rheumatic Fever 60 0.031
341
QFV001 Q Fever 60 0.031
342
P THL005 Thalassemia 60 0.031
343
P RBL001 Rubella 59 0.031
344
PRT013 Portal Hypertension 59 0.031
345
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.031
346
P BND020 Bone Disease 59 0.031
347
c DNG003 Dengue Disease 59 0.031
348
ADN018 Adenoma 59 0.031
349
P PLY006 Polydactyly 59 0.031
350
ANR040 Aneurysm 59 0.031
351
c SVR003 Severe Congenital Neutropenia 59 0.031
352
PPT005 Peptic Ulcer Disease 59 0.031
353
SRC027 Sarcoma, Synovial 58 0.031
354
P ANP001 Anaplastic Large Cell Lymphoma 58 0.031
355
GLB001 Gilbert Syndrome 58 0.031
356
ANT024 Anthrax Disease 58 0.031
357
P BCL017 B-Cell Lymphoma 58 0.031
358
CRD132 Cardiac Conduction Defect 58 0.031
359
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.031
360
DSS008 Disease of Mental Health 58 0.031
361
P MMP001 Mumps 58 0.031
362
MNT002 Mental Depression 58 0.031
363
CNS004 Constipation 58 0.031
364
P INF032 Infertility 57 0.031
365
P UVT001 Uveitis 57 0.031
366
MCR013 Microphthalmia 57 0.031
367
IRN002 Iron Metabolism Disease 57 0.031
368
CHK001 Chikungunya 57 0.031
369
P RHN004 Rhinitis 57 0.031
370
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.031
371
BLR008 Bilirubin Metabolic Disorder 57 0.031
372
CYT008 Cytomegalovirus Infection 57 0.031
373
P BPL003 Bipolar Disorder 56 0.031
374
P CHN012 Chondrosarcoma 56 0.031
375
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.031
376
P NRF002 Neurofibromatosis 56 0.031
377
c CCK008 Cockayne Syndrome a 55 0.031
378
MMB001 Membranoproliferative Glomerulonephritis 55 0.031
379
NPH009 Nephrolithiasis 55 0.031
380
P MYP006 Myopia 55 0.031
381
CHR100 Chronic Ulcer of Skin 55 0.031
382
P SBS003 Substance Abuse 55 0.031
383
P HYP076 Hyperthyroidism 55 0.031
384
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.031
385
END040 Endogenous Depression 55 0.031
386
INT007 Intermediate Coronary Syndrome 55 0.031
387
GLS001 Gliosarcoma 54 0.031
388
AMN003 Amnestic Disorder 54 0.031
389
c CCK007 Cockayne Syndrome B 54 0.031
390
P ART021 Arteriosclerosis 54 0.031
391
DBT010 Diabetic Neuropathy 54 0.031
392
LYM040 Lymphoblastic Lymphoma 54 0.031
393
NNL006 Non-Alcoholic Steatohepatitis 54 0.031
394
c SPN294 Spinocerebellar Ataxia 1 53 0.031
395
c LNG048 Long Qt Syndrome 3 53 0.031
396
P TCD001 Tic Disorder 53 0.031
397
P HMC002 Homocystinuria 53 0.031
398
ACR014 Acral Lentiginous Melanoma 53 0.031
399
P HML001 Hemolytic-Uremic Syndrome 53 0.031
400
GTR002 Goiter 53 0.031
401
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.031
402
NRT001 Neurotic Disorder 53 0.031
403
GST023 Gastric Ulcer 53 0.031
404
c FML191 Familial Long Qt Syndrome 53 0.031
405
CHR073 Choreatic Disease 52 0.031
406
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.031
407
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.031
408
DMY004 Demyelinating Disease 52 0.031
409
P PRG013 Paraganglioma 52 0.031
410
c VRL010 Viral Hepatitis 52 0.031
411
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
412
PST011 Pustulosis of Palm and Sole 52 0.031
413
P MSC003 Muscular Atrophy 52 0.031
414
BWN001 Bowen-Conradi Syndrome 52 0.031
415
LGN006 Legionnaire Disease 52 0.031
416
PTH003 Pathologic Nystagmus 52 0.031
417
HYP014 Hyperuricemia 52 0.031
418
ONC002 Onchocerciasis 52 0.031
419
c ACT135 Acute Graft Versus Host Disease 52 0.031
421
OCL069 Ocular Motor Apraxia 51 0.031
422
KRT009 Keratosis 51 0.031
423
c PNC106 Pancreatic Agenesis 1 51 0.031
424
c PRM108 Primary Progressive Multiple Sclerosis 51 0.031
425
P AST007 Astrocytoma 51 0.031
426
TLR001 Tularemia 51 0.031
427
END086 End Stage Renal Disease 51 0.031
428
CRV040 Cervix Carcinoma 51 0.031
429
RTN003 Retinal Ischemia 50 0.031
430
P ECL001 Eclampsia 50 0.031
431
HRT031 Hartnup Disorder 50 0.031
432
CRN030 Coronary Stenosis 50 0.031
433
c SVR005 Severe Pre-Eclampsia 50 0.031
434
THY125 Thyroid Gland Medullary Carcinoma 50 0.031
435
VTR016 Vater/vacterl Association 50 0.031
436
TRY001 Trypanosomiasis 50 0.031
437
P OBS001 Obstructive Jaundice 50 0.031
438
MTB004 Metabolic Acidosis 50 0.031
439
HYP017 Hypophosphatemia 50 0.031
440
P ATR005 Atrophic Gastritis 50 0.031
441
ENT004 Enthesopathy 49 0.031
442
P IGN003 Iga Nephropathy 1 49 0.031
443
PRS129 Prostatic Hyperplasia, Benign 49 0.031
444
SCT005 Scott Syndrome 49 0.031
445
IMP004 Impetigo 49 0.031
446
BNR002 Bone Resorption Disease 48 0.031
447
CHL061 Childhood Leukemia 48 0.031
448
RFR010 Refractory Anemia 48 0.031
449
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.031
450
PNC034 Pancreas Disease 48 0.031
451
SPL018 Splenomegaly 48 0.031
452
END062 Endometrial Hyperplasia 48 0.031
453
IGG001 Iga Glomerulonephritis 48 0.031
454
PNC013 Pancreatic Ductal Carcinoma 48 0.031
455
MLT006 Multidrug-Resistant Tuberculosis 48 0.031
456
CRC014 Carcinoid Tumors, Intestinal 47 0.031
457
CRN027 Corneal Neovascularization 47 0.031
458
P KRN004 Kernicterus 47 0.031
459
P MTC010 Mitochondrial Dna Depletion Syndrome 47 0.031
460
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.031
461
RTN023 Retinitis 46 0.031
462
LPD009 Lipid Storage Disease 46 0.031
463
EXS001 Exostosis 46 0.031
464
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.031
465
P HYP733 Hypercalciuria, Absorptive, 2 45 0.031
466
HMR023 Hemorrhagic Cystitis 45 0.031
467
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.031
468
SPS057 Spasticity 45 0.031
469
PTT037 Pituitary Tumors 44 0.031
470
c PCH010 Pachyonychia Congenita 3 44 0.031
471
P MTC004 Mitochondrial Encephalomyopathy 44 0.031
472
DWR001 Dwarfism 44 0.031
473
P HYP111 Hyperprolinemia 44 0.031
474
c HYP272 Hypercholesterolemia, Familial, 3 44 0.031
475
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.031
476
c LBR019 Leber Congenital Amaurosis 9 44 0.031
477
END085 Endometrial Serous Adenocarcinoma 44 0.031
478
CRB090 Cerebral Hypoxia 44 0.031
479
RTC009 Reticulum Cell Sarcoma 43 0.031
480
P CRN026 Corneal Edema 43 0.031
481
ORL015 Oral Squamous Cell Carcinoma 43 0.031
482
VCT001 Vacterl Association 42 0.031
483
MST004 Mast Cell Neoplasm 42 0.031
484
PNM013 Pneumococcal Meningitis 42 0.031
485
NRR001 Neuroretinitis 42 0.031
486
c MJR024 Major Affective Disorder 9 41 0.031
487
ALC005 Alcoholic Pancreatitis 40 0.031
488
P ADV001 Advanced Sleep Phase Syndrome 40 0.031
489
IMM001 Immune-Complex Glomerulonephritis 40 0.031
490
ASP030 Aspirin Resistance 39 0.031
491
PPL035 Papillary Thyroid Microcarcinoma 39 0.031
492
c ACT004 Acute Diarrhea 39 0.031
493
48X005 48,xyyy 39 0.031
494
P XNT004 Xanthinuria 39 0.031
495
AML001 Amelanotic Melanoma 39 0.031
496
TRN007 Transsexualism 39 0.031
497
EXT007 Extracutaneous Mastocytoma 38 0.031
498
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 38 0.031
499
c MJR022 Major Affective Disorder 8 38 0.031
500
P FML187 Familial Hypertension 37 0.031
501
CRD016 Cardiac Rupture 37 0.031
502
TLC001 Telecanthus 35 0.031
503
CHR178 Chromosomal Triplication 35 0.031
504
c MCR245 Microphthalmia, Syndromic 8 34 0.031
506
P ALB003 Albinism-Deafness Syndrome 31 0.031
507
c HRD142 Hereditary Xanthinuria 31 0.031
508
PLR005 Pleuropneumonia 31 0.031
509
CRT020 Cortisone Reductase Deficiency 31 0.031
510
PLY150 Polykaryocytosis Inducer 31 0.031
511
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 30 0.031
512
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 29 0.031
514
ARG004 Argyria 27 0.031
515
DGT002 Digital Clubbing, Isolated Congenital 27 0.031
516
CHL079 Children's Interstitial Lung Disease 26 0.031
517
c RNG024 Ring Chromosome 8 26 0.031
518
PRK088 Parkinson Disease, Mitochondrial 26 0.031
519
PRQ002 Paraquat Poisoning 26 0.031
520
URT049 Urate Oxidase, Pseudogene 25 0.031
521
NRM022 Neurometabolic Disease 25 0.031
522
TXC004 Toxic Diffuse Goiter 24 0.031
523
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 21 0.031
524
LCT008 Lactate Dehydrogenase Deficiency 19 0.031
525
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.031
526
PRS119 Persistent Genital Arousal Disorder 18 0.031
528
MYL078 Myelodysplastic Syndrome with Single Lineage Dysplasia 13 0.031
529
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.031
531
c PRM317 Primary Qualitative or Quantitative Defects of Alpha-Dystroglycan 9 0.031
532
c LCT020 Lactic Acidosis, Chronic Adult Form 8 0.031
533
QLT016 Qualitative or Quantitative Defects of Protein Involved in O-Glycosylation of Alpha-Dystroglycan 8 0.031
534
KNR001 Koone Rizzo Elias Syndrome 8 0.031
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