Search results for NAD

525 hits were found for NAD

# Family MCID Name MIFTS Score
1
P HYP769 Hyperlysinemia, Type I 38 3.887
2
NTR027 Neutrophil Actin Dysfunction 23 3.225
3
P VRT014 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1 21 3.211
4
CNG532 Congenital Vertebral-Cardiac-Renal Anomalies Syndrome 16 3.160
5
P SJG002 Sjogren-Larsson Syndrome 54 2.326
6
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 18 2.297
7
NDH002 Nad Hx Dehydratase Deficiency 3 2.297
8
NDH003 Nad Hx Epimerase Deficiency 3 2.297
9
DPH001 Diphtheria 61 0.209
10
PRT037 Pertussis 66 0.186
11
P LNG032 Lung Cancer 99 0.164
12
P CLR023 Colorectal Cancer 100 0.161
13
AGN016 Aging 58 0.158
14
P VSC007 Vascular Disease 65 0.151
15
CHL014 Cholera 58 0.151
16
FTT001 Fatty Liver Disease 63 0.148
17
HMP009 Haemophilus Influenzae 46 0.134
18
P PNC035 Pancreatic Cancer 86 0.122
19
c MCR113 Microvascular Complications of Diabetes 3 55 0.122
20
c MCR120 Microvascular Complications of Diabetes 7 48 0.122
21
c MCR130 Microvascular Complications of Diabetes 6 42 0.122
22
c MCR133 Microvascular Complications of Diabetes 4 42 0.122
23
P BRS047 Breast Cancer 99 0.118
24
HYP066 Hyperglycemia 63 0.118
25
ISC004 Ischemia 62 0.118
26
WLL004 Wallerian Degeneration 40 0.118
27
c HYP836 Hypercholesterolemia, Familial, 1 74 0.114
28
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.114
29
P LYM031 Lymphocytic Leukemia 56 0.114
30
BRN071 Brain Injury 51 0.114
31
P ALZ034 Alzheimer Disease 90 0.109
32
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 20 0.109
33
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.104
34
HPT022 Hepatoblastoma 58 0.104
35
ATH013 Atherosclerosis Susceptibility 68 0.100
36
HLX001 Helix Syndrome 46 0.100
37
P HPT023 Hepatocellular Carcinoma 99 0.095
38
P MYC084 Mycobacterium Tuberculosis 1 69 0.095
39
P LKM002 Leukemia 69 0.095
40
P LKM062 Leukemia, Acute Lymphoblastic 68 0.095
41
ANX004 Anoxia 44 0.095
42
CRB004 Cerebral Artery Occlusion 38 0.095
43
P BLD134 Bladder Cancer 79 0.089
44
P HNT016 Huntington Disease 72 0.089
45
P LVR013 Liver Disease 71 0.089
46
ART002 Arts Syndrome 63 0.089
47
HYP266 Hypoxia 58 0.089
48
P MTC069 Mitochondrial Disorders 57 0.089
49
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.089
50
c LKM061 Leukemia, Acute Myeloid 84 0.083
51
P ADN016 Adenocarcinoma 65 0.083
52
P PRP019 Peripheral Nervous System Disease 64 0.083
53
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.083
54
P NRP001 Neuropathy 57 0.083
55
TRM010 Traumatic Brain Injury 54 0.083
56
ESP021 Esophageal Cancer 90 0.077
57
P LNG064 Lung Cancer Susceptibility 3 79 0.077
58
P HRT032 Heart Disease 78 0.077
59
GLB002 Glioblastoma 74 0.077
60
P SKN015 Skin Carcinoma 67 0.077
61
P NRB010 Neuroblastoma 1 66 0.077
62
GLB015 Glioblastoma Multiforme 60 0.077
63
PHR003 Pharyngitis 56 0.077
64
47X002 47,xyy 49 0.077
65
PRM329 Premature Aging 41 0.077
66
ALL014 Allergic Encephalomyelitis 40 0.077
67
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.077
68
P PRS040 Prostate Cancer 97 0.070
69
P OVR042 Ovarian Cancer 89 0.070
70
END057 Endometrial Cancer 74 0.070
71
CNG034 Congestive Heart Failure 69 0.070
72
MLN008 Melanoma 68 0.070
73
P MSC005 Muscular Dystrophy 68 0.070
74
P MCR115 Microvascular Complications of Diabetes 5 67 0.070
75
c SML038 Small Cell Cancer of the Lung 67 0.070
76
P PLM036 Pulmonary Fibrosis 66 0.070
77
P CCK001 Cockayne Syndrome 66 0.070
78
IDP011 Idiopathic Interstitial Pneumonia 65 0.070
79
LPD008 Lipid Metabolism Disorder 64 0.070
80
ATM095 Autoimmune Disease 62 0.070
81
P CRN300 Coronary Heart Disease 1 59 0.070
82
P BRS044 Breast Adenocarcinoma 59 0.070
83
MTC005 Mitochondrial Metabolism Disease 50 0.070
84
NCR007 Necrotizing Fasciitis 47 0.070
85
FSC004 Fasciitis 47 0.070
86
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.070
87
CND006 Candida Glabrata 33 0.070
88
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.070
89
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.063
90
MYL069 Myeloma, Multiple 85 0.063
91
P ATX030 Ataxia-Telangiectasia 83 0.063
92
c LKM071 Leukemia, Chronic Lymphocytic 81 0.063
93
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.063
94
P SCH015 Schizophrenia 76 0.063
95
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.063
96
P CHR012 Chronic Granulomatous Disease 69 0.063
97
BRK010 Burkitt Lymphoma 68 0.063
98
P CRN018 Coronary Artery Anomaly 67 0.063
99
CHG001 Chagas Disease 66 0.063
100
MSC007 Muscle Hypertrophy 65 0.063
101
CLN015 Colon Adenocarcinoma 65 0.063
102
LSH001 Leishmaniasis 64 0.063
103
P GLM045 Glioma 64 0.063
104
ACT119 Acute Promyelocytic Leukemia 63 0.063
105
TXC005 Toxic Shock Syndrome 63 0.063
106
P MYL006 Myeloid Leukemia 61 0.063
107
SQM006 Squamous Cell Carcinoma 60 0.063
108
P FBR017 Fibrosarcoma 57 0.063
109
P LTR001 Lateral Sclerosis 56 0.063
110
GLC003 Glucose Intolerance 55 0.063
111
SPP010 Suppressor of Tumorigenicity 3 54 0.063
112
TLN003 Telangiectasis 53 0.063
113
LYM019 Lymphosarcoma 48 0.063
114
GLL048 Glial Tumor 48 0.063
115
P PLL002 Pellagra 47 0.063
116
P KLZ004 Kala-Azar 1 43 0.063
117
STR077 Streptococcal Toxic-Shock Syndrome 38 0.063
118
HRW001 Hair Whorl 36 0.063
119
c LKM004 Leukemia, B-Cell, Chronic 35 0.063
120
STN013 Stenotrophomonas Maltophilia Infection 26 0.063
121
P GST053 Gastric Cancer 85 0.055
122
CRV035 Cervical Cancer 77 0.055
123
P PRK057 Parkinson Disease, Late-Onset 77 0.055
124
c HPT073 Hepatitis C Virus 74 0.055
125
c LKM063 Leukemia, Chronic Myeloid 74 0.055
126
P MLT020 Multiple Sclerosis 73 0.055
127
P KDN018 Kidney Disease 73 0.055
128
P PHC003 Pheochromocytoma 71 0.055
129
CHL065 Cholangiocarcinoma 68 0.055
130
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.055
131
OST159 Osteogenic Sarcoma 67 0.055
132
P DBT009 Diabetes Mellitus 66 0.055
133
P HML002 Hemolytic Anemia 64 0.055
134
P NTR004 Neutropenia 64 0.055
135
P MYP004 Myopathy 63 0.055
136
TRN015 Transient Cerebral Ischemia 62 0.055
137
CRC021 Carcinosarcoma 62 0.055
138
THY029 Thyroid Carcinoma 62 0.055
139
ART140 Arteries, Anomalies of 60 0.055
140
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.055
141
c ACT075 Acute Myocardial Infarction 59 0.055
142
c ACT210 Acute Respiratory Distress Syndrome 59 0.055
143
P GLM007 Glomerulonephritis 58 0.055
144
P GST044 Gastritis 58 0.055
145
P INF037 Inflammatory Bowel Disease 57 0.055
146
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.055
147
APP015 Apparent Mineralocorticoid Excess 56 0.055
148
P RTN016 Retinal Degeneration 56 0.055
149
INT079 Intrahepatic Cholangiocarcinoma 54 0.055
150
P RTN018 Retinal Disease 53 0.055
151
LNG031 Lung Benign Neoplasm 52 0.055
152
P LCT001 Lactic Acidosis 52 0.055
153
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.055
154
ADR040 Adrenal Gland Pheochromocytoma 51 0.055
155
ATS010 Autosomal Recessive Disease 49 0.055
156
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 47 0.055
157
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.055
158
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.055
159
PST092 Posttransplant Acute Limbic Encephalitis 29 0.055
160
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.045
162
c HYP595 Hypertension, Essential 87 0.045
163
MLR004 Malaria 82 0.045
164
c FNC027 Fanconi Anemia, Complementation Group a 81 0.045
165
OST012 Osteoarthritis 80 0.045
166
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.045
167
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.045
168
SVR004 Severe Combined Immunodeficiency 74 0.045
169
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.045
170
HMN044 Human Immunodeficiency Virus Type 1 73 0.045
171
PHN003 Phenylketonuria 73 0.045
172
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.045
173
MYL009 Myelodysplastic Syndrome 72 0.045
174
CRB039 Cerebrovascular Disease 71 0.045
175
LYM133 Lymphoma, Hodgkin, Classic 70 0.045
176
P LYM118 Lymphoma 70 0.045
177
c EXD008 Exudative Vitreoretinopathy 1 69 0.045
178
c ATS007 Autism Spectrum Disorder 69 0.045
179
P PLM037 Pulmonary Hypertension 69 0.045
180
LGH007 Leigh Syndrome 69 0.045
181
PNC129 Pancreatic Adenocarcinoma 69 0.045
182
P ATS364 Autism 68 0.045
183
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.045
184
HYP056 Hypoglycemia 68 0.045
185
P DRM053 Dermatitis, Atopic 68 0.045
186
P ATR011 Atrial Fibrillation 67 0.045
187
P THR014 Thrombocytopenia 67 0.045
188
BRR014 Barrett Esophagus 67 0.045
189
GST040 Gastric Adenocarcinoma 67 0.045
190
ANG054 Angina Pectoris 66 0.045
191
P TRN020 Turner Syndrome 66 0.045
192
DPR016 Depression 64 0.045
193
CLR108 Colorectal Adenoma 64 0.045
194
HMT002 Hematologic Cancer 64 0.045
195
DRM006 Dermatitis 63 0.045
196
c PRC016 Pre-Eclampsia 63 0.045
197
P END044 Endometriosis 63 0.045
198
SPN186 Spinal Cord Injury 63 0.045
199
P PNC044 Pancreatitis 61 0.045
200
HLC007 Helicobacter Pylori Infection 61 0.045
201
c ACT071 Acute Kidney Failure 60 0.045
202
P MYC008 Myocarditis 60 0.045
203
INS001 Insulinoma 60 0.045
204
c ACT073 Acute Leukemia 59 0.045
205
P CYS018 Cystitis 59 0.045
206
P PLY011 Polycystic Ovary Syndrome 58 0.045
207
TRD006 Tardive Dyskinesia 58 0.045
208
P ALC033 Alcohol Use Disorder 58 0.045
209
LYM027 Lymphopenia 58 0.045
210
SCH014 Schistosomiasis 57 0.045
211
P PRN023 Prion Disease 57 0.045
212
BRN056 Bronchopulmonary Dysplasia 57 0.045
213
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.045
214
HYP060 Hyperinsulinism 55 0.045
215
HYP005 Hypokalemia 55 0.045
216
P ICH004 Ichthyosis 55 0.045
217
P DRR001 Diarrhea 55 0.045
218
VSC003 Visceral Leishmaniasis 55 0.045
219
PRS045 Prostatic Hypertrophy 55 0.045
220
P RCT021 Rectum Cancer 54 0.045
221
HMC014 Homocysteinemia 54 0.045
222
IMP005 Impotence 53 0.045
223
P MTC133 Mitochondrial Myopathy 53 0.045
224
DNT012 Dental Caries 52 0.045
225
PRS021 Prostatic Adenoma 52 0.045
226
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.045
227
CHR005 Chorioamnionitis 51 0.045
228
LMB062 Limb Ischemia 50 0.045
229
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.045
230
ADN009 Adenosquamous Carcinoma 50 0.045
231
RTN020 Retinal Vascular Disease 49 0.045
232
P RNV001 Renovascular Hypertension 49 0.045
233
HST006 Histidinemia 49 0.045
234
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.045
235
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.045
236
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.045
237
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.045
238
SLP001 Sleeping Sickness 47 0.045
239
CHR074 Choriocarcinoma 47 0.045
240
HDN002 Head Injury 47 0.045
241
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.045
242
CYT002 Cytokine Deficiency 46 0.045
243
c MLG068 Malignant Glioma 46 0.045
244
GRN017 Granulocytopenia 46 0.045
245
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.045
246
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.045
247
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.045
248
c SPR086 Spermatogenic Failure 3 41 0.045
250
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.045
251
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 36 0.045
252
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.045
253
PPL052 Papillomatosis, Confluent and Reticulated 34 0.045
254
24D001 2,4-Dienoyl-Coa Reductase Deficiency 32 0.045
255
c LNG109 Lung Cancer Susceptibility 1 27 0.045
256
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 27 0.045
257
TRY004 Trypanosomiasis, Human East-African 25 0.045
258
P ENC069 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 1 24 0.045
259
HYP171 Hyperphenylalaninemia Due to Dehydratase Deficiency 16 0.045
260
c SYS001 Systemic Lupus Erythematosus 88 0.032
261
c DLT002 Dilated Cardiomyopathy 81 0.032
262
AST005 Asthma 80 0.032
263
INS024 Insulin-Like Growth Factor I 79 0.032
264
DFC004 Deficiency Anemia 77 0.032
265
c CWD006 Cowden Syndrome 1 76 0.032
266
c ATR087 Atrial Standstill 1 76 0.032
267
P APL001 Aplastic Anemia 76 0.032
268
ULC004 Ulcerative Colitis 75 0.032
269
CRH001 Crohn's Disease 75 0.032
270
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.032
271
SCK003 Sickle Cell Anemia 74 0.032
272
ACR006 Aceruloplasminemia 74 0.032
273
P EPL164 Epilepsy 73 0.032
274
P CNR004 Cone-Rod Dystrophy 2 72 0.032
275
PLM001 Pulmonary Tuberculosis 72 0.032
276
P ART022 Arthritis 71 0.032
277
P BRG001 Brugada Syndrome 70 0.032
278
P HYP086 Hypothyroidism 70 0.032
279
RCK004 Rickets 70 0.032
280
MNT001 Mantle Cell Lymphoma 69 0.032
281
P HPT021 Hepatitis 69 0.032
282
P MJR001 Major Depressive Disorder 69 0.032
283
ALL003 Allergic Rhinitis 69 0.032
284
P LNG028 Long Qt Syndrome 68 0.032
285
c CHR684 Chronic Kidney Disease 68 0.032
286
P DMN002 Dementia 68 0.032
287
ALC007 Alcohol Dependence 68 0.032
288
THY111 Thyroid Carcinoma, Familial Medullary 68 0.032
289
CHD001 Chediak-Higashi Syndrome 68 0.032
290
P MPL001 Maple Syrup Urine Disease 68 0.032
291
SKN019 Skin Melanoma 68 0.032
292
c BSL007 Basal Cell Carcinoma 68 0.032
293
P LBR001 Leber Congenital Amaurosis 67 0.032
294
P MNN013 Meningitis 67 0.032
295
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.032
296
PRT036 Peritonitis 66 0.032
297
P BLD062 Bile Duct Cancer 66 0.032
298
P CWD010 Cowden Syndrome 66 0.032
299
P PRD008 Periodontitis 66 0.032
300
DSS008 Disease of Mental Health 66 0.032
301
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.032
302
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.032
303
c ATS013 Autosomal Recessive Congenital Ichthyosis 65 0.032
304
ALL026 Allergic Hypersensitivity Disease 65 0.032
305
KRN002 Kearns-Sayre Syndrome 64 0.032
306
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.032
307
SKN016 Skin Disease 64 0.032
308
HTC003 Hutchinson-Gilford Progeria Syndrome 64 0.032
309
P PSR002 Psoriasis 63 0.032
310
c ACT068 Acute Cystitis 63 0.032
311
CLT003 Colitis 63 0.032
312
GLC006 Galactosemia 63 0.032
313
MCR013 Microphthalmia 62 0.032
314
P RHB003 Rhabdomyosarcoma 62 0.032
315
P LPS004 Lupus Erythematosus 62 0.032
316
LNG099 Lung Disease 62 0.032
317
P THL005 Thalassemia 62 0.032
318
NRM005 Neuromuscular Disease 62 0.032
319
P ESP024 Esophagitis 62 0.032
320
P SNS001 Sensorineural Hearing Loss 62 0.032
321
RTN017 Retinal Detachment 62 0.032
322
c HPT001 Hepatitis C 62 0.032
323
P INT143 Interstitial Cystitis 62 0.032
324
c SCL052 Scleroderma, Familial Progressive 62 0.032
325
CRD223 Cardiac Arrhythmia 61 0.032
326
CHL068 Cholestasis 61 0.032
327
INT066 Interstitial Lung Disease 61 0.032
328
c DNG003 Dengue Disease 61 0.032
329
PRT013 Portal Hypertension 61 0.032
330
ACQ007 Acquired Immunodeficiency Syndrome 61 0.032
331
P BCL017 B-Cell Lymphoma 61 0.032
332
NTR005 Nutritional Deficiency Disease 61 0.032
333
MSL001 Measles 61 0.032
334
LSC001 Lesch-Nyhan Syndrome 61 0.032
335
c ACT027 Acute Pancreatitis 60 0.032
336
CHL123 Chlamydia 60 0.032
337
PPT005 Peptic Ulcer Disease 60 0.032
338
ALC006 Alcoholic Hepatitis 60 0.032
339
MNT002 Mental Depression 60 0.032
340
P KDN017 Kidney Cancer 60 0.032
341
P CTS001 Cutis Laxa 60 0.032
342
BND020 Bone Disease 60 0.032
343
END030 End Stage Renal Failure 60 0.032
344
SRC027 Sarcoma, Synovial 60 0.032
345
ADN018 Adenoma 60 0.032
346
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.032
347
P RHN004 Rhinitis 59 0.032
348
P BPL003 Bipolar Disorder 59 0.032
349
c SVR003 Severe Congenital Neutropenia 59 0.032
350
CNS004 Constipation 59 0.032
351
P PLY006 Polydactyly 58 0.032
352
P UVT001 Uveitis 58 0.032
353
CYT008 Cytomegalovirus Infection 58 0.032
354
P MYP006 Myopia 58 0.032
355
PLM031 Poliomyelitis 58 0.032
356
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 58 0.032
357
IRN002 Iron Metabolism Disease 58 0.032
358
QFV001 Q Fever 58 0.032
359
ERY051 Erythroleukemia, Familial 58 0.032
360
GLB001 Gilbert Syndrome 58 0.032
361
BLR008 Bilirubin Metabolic Disorder 58 0.032
362
INT007 Intermediate Coronary Syndrome 58 0.032
363
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.032
364
PRM236 Primary Biliary Cholangitis 57 0.032
365
P MMP001 Mumps 57 0.032
366
P CHN012 Chondrosarcoma 57 0.032
367
P PLY147 Polydactyly, Postaxial, Type A1 57 0.032
368
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.032
369
ANT024 Anthrax Disease 56 0.032
370
RHM027 Rheumatic Disease 56 0.032
371
P RBL001 Rubella 56 0.032
372
c VRL010 Viral Hepatitis 56 0.032
373
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.032
374
DBT010 Diabetic Neuropathy 56 0.032
375
GLS001 Gliosarcoma 56 0.032
376
P ART021 Arteriosclerosis 56 0.032
377
RHM001 Rheumatic Fever 56 0.032
378
P TCD001 Tic Disorder 55 0.032
379
AMN003 Amnestic Disorder 55 0.032
380
c SPN294 Spinocerebellar Ataxia 1 55 0.032
381
END040 Endogenous Depression 55 0.032
382
CHK001 Chikungunya 55 0.032
383
P HYP076 Hyperthyroidism 55 0.032
384
P PRM006 Primary Biliary Cirrhosis 54 0.032
385
MMB001 Membranoproliferative Glomerulonephritis 54 0.032
386
GTR002 Goiter 54 0.032
387
LYM040 Lymphoblastic Lymphoma 54 0.032
388
P HML001 Hemolytic-Uremic Syndrome 54 0.032
389
DMY004 Demyelinating Disease 54 0.032
390
MSC190 Muscular Disease 54 0.032
391
c FML191 Familial Long Qt Syndrome 54 0.032
392
PTH003 Pathologic Nystagmus 53 0.032
393
P PRG013 Paraganglioma 53 0.032
394
CHR100 Chronic Ulcer of Skin 53 0.032
395
P ECL001 Eclampsia 53 0.032
396
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.032
397
OCL069 Ocular Motor Apraxia 53 0.032
398
NRT001 Neurotic Disorder 53 0.032
399
GST023 Gastric Ulcer 53 0.032
400
NNL006 Non-Alcoholic Steatohepatitis 53 0.032
401
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.032
402
CHR073 Choreatic Disease 52 0.032
403
HYP014 Hyperuricemia 52 0.032
404
RTN003 Retinal Ischemia 52 0.032
405
THY125 Thyroid Gland Medullary Carcinoma 52 0.032
406
P HMC002 Homocystinuria 52 0.032
407
CRV040 Cervix Carcinoma 52 0.032
408
ACR014 Acral Lentiginous Melanoma 52 0.032
409
KRT009 Keratosis 52 0.032
410
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.032
411
P AST007 Astrocytoma 52 0.032
412
PNC034 Pancreas Disease 51 0.032
414
BNR002 Bone Resorption Disease 51 0.032
415
VTR016 Vater/vacterl Association 51 0.032
416
c CCK008 Cockayne Syndrome a 51 0.032
417
PST011 Pustulosis of Palm and Sole 51 0.032
418
c SVR005 Severe Pre-Eclampsia 50 0.032
419
P IGN003 Iga Nephropathy 1 50 0.032
420
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.032
421
MNC006 Monoclonal Gammopathy of Uncertain Significance 50 0.032
422
TRY001 Trypanosomiasis 50 0.032
423
ACR041 Acromelic Frontonasal Dysostosis 50 0.032
424
c PNC106 Pancreatic Agenesis 1 50 0.032
425
ONC002 Onchocerciasis 50 0.032
426
IGG001 Iga Glomerulonephritis 50 0.032
427
RFR010 Refractory Anemia 50 0.032
428
c LNG048 Long Qt Syndrome 3 50 0.032
429
CRN030 Coronary Stenosis 49 0.032
430
PRS129 Prostatic Hyperplasia, Benign 49 0.032
431
c PRM108 Primary Progressive Multiple Sclerosis 49 0.032
432
CHL061 Childhood Leukemia 49 0.032
433
P ATR005 Atrophic Gastritis 49 0.032
434
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.032
435
END062 Endometrial Hyperplasia 49 0.032
436
CRC014 Carcinoid Tumors, Intestinal 49 0.032
437
LPD009 Lipid Storage Disease 49 0.032
438
P OBS001 Obstructive Jaundice 49 0.032
439
BWN001 Bowen-Conradi Syndrome 49 0.032
440
SPL018 Splenomegaly 48 0.032
441
MTB004 Metabolic Acidosis 48 0.032
442
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.032
443
CRN027 Corneal Neovascularization 48 0.032
444
LGN006 Legionnaire Disease 48 0.032
445
SCT005 Scott Syndrome 48 0.032
446
c CCK007 Cockayne Syndrome B 48 0.032
447
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.032
448
HYP017 Hypophosphatemia 48 0.032
449
P KRN004 Kernicterus 47 0.032
450
HRT031 Hartnup Disorder 47 0.032
451
PTT037 Pituitary Tumors 47 0.032
452
IMP004 Impetigo 47 0.032
453
P MTC010 Mitochondrial Dna Depletion Syndrome 47 0.032
454
RTN023 Retinitis 46 0.032
455
NRR001 Neuroretinitis 46 0.032
456
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.032
457
EXS001 Exostosis 46 0.032
458
ENT004 Enthesopathy 46 0.032
459
PNM013 Pneumococcal Meningitis 45 0.032
460
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.032
461
DWR001 Dwarfism 45 0.032
462
CRB090 Cerebral Hypoxia 45 0.032
463
RTC009 Reticulum Cell Sarcoma 45 0.032
464
TLR001 Tularemia 44 0.032
465
c HYP272 Hypercholesterolemia, Familial, 3 44 0.032
466
ORL015 Oral Squamous Cell Carcinoma 44 0.032
467
MTC004 Mitochondrial Encephalomyopathy 44 0.032
468
PNC013 Pancreatic Ductal Carcinoma 44 0.032
469
c PCH010 Pachyonychia Congenita 3 43 0.032
470
VCT001 Vacterl Association 43 0.032
471
c LBR019 Leber Congenital Amaurosis 9 43 0.032
472
ASP030 Aspirin Resistance 42 0.032
473
c MJR024 Major Affective Disorder 9 42 0.032
474
PLR005 Pleuropneumonia 42 0.032
475
TRN007 Transsexualism 41 0.032
476
UTR011 Uterine Corpus Serous Adenocarcinoma 41 0.032
477
MST004 Mast Cell Neoplasm 40 0.032
478
PPL035 Papillary Thyroid Microcarcinoma 40 0.032
479
HMR023 Hemorrhagic Cystitis 40 0.032
480
IMM001 Immune-Complex Glomerulonephritis 40 0.032
481
GNT029 Genetic Hypertension 39 0.032
482
c MJR022 Major Affective Disorder 8 39 0.032
483
P HYP111 Hyperprolinemia 39 0.032
484
EXT007 Extracutaneous Mastocytoma 39 0.032
485
SPS057 Spasticity 38 0.032
486
AML001 Amelanotic Melanoma 38 0.032
487
HRN029 Hearing Loss, Noise-Induced 38 0.032
488
c ACT004 Acute Diarrhea 38 0.032
489
48X005 48,xyyy 37 0.032
490
ALC005 Alcoholic Pancreatitis 37 0.032
491
CHR178 Chromosomal Triplication 36 0.032
492
c CHR682 Chronic Bilirubin Encephalopathy 36 0.032
493
CRT020 Cortisone Reductase Deficiency 35 0.032
494
P FML187 Familial Hypertension 35 0.032
496
TLC001 Telecanthus 34 0.032
497
c MCR245 Microphthalmia, Syndromic 8 33 0.032
498
CRD016 Cardiac Rupture 33 0.032
499
PLY150 Polykaryocytosis Inducer 31 0.032
500
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 31 0.032
501
P ALB003 Albinism-Deafness Syndrome 31 0.032
503
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 29 0.032
504
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 29 0.032
505
ARG004 Argyria 28 0.032
506
DGT002 Digital Clubbing, Isolated Congenital 28 0.032
507
CHL079 Children's Interstitial Lung Disease 27 0.032
508
TXC004 Toxic Diffuse Goiter 27 0.032
509
URT049 Urate Oxidase, Pseudogene 26 0.032
510
NRM022 Neurometabolic Disease 26 0.032
511
PRQ002 Paraquat Poisoning 25 0.032
512
PRK088 Parkinson Disease, Mitochondrial 22 0.032
513
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 22 0.032
514
c ENC066 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 2 20 0.032
515
PRS119 Persistent Genital Arousal Disorder 19 0.032
516
c LKM055 Leukemia, Acute Lymphoblastic 2 17 0.032
517
LCT008 Lactate Dehydrogenase Deficiency 16 0.032
519
CNG393 Congenital Muscular Dystrophy with Hyperlaxity 12 0.032
520
RFR006 Refractory Cytopenia with Unilineage Dysplasia 12 0.032
522
c PRM317 Primary Qualitative or Quantitative Defects of Alpha-Dystroglycan 9 0.032
523
QLT016 Qualitative or Quantitative Defects of Protein Involved in O-Glycosylation of Alpha-Dystroglycan 8 0.032
524
c LCT020 Lactic Acidosis, Chronic Adult Form 8 0.032
525
KNR001 Koone Rizzo Elias Syndrome 8 0.032
Content
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