Search results for Manganese

827 hits were found for Manganese

# Family MCID Name MIFTS Score
1
MNG007 Manganese Poisoning 28 5.417
2
P HYP821 Hypermanganesemia with Dystonia 23 2.682
3
DSR032 Disorder of Manganese Transport 7 2.643
4
P TRM003 Tremor 55 0.208
5
IRN002 Iron Metabolism Disease 58 0.198
6
P ENC018 Encephalopathy 64 0.189
7
P PRK057 Parkinson Disease, Late-Onset 77 0.182
8
CHL068 Cholestasis 61 0.176
9
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.171
10
P DYS154 Dystonia 65 0.163
11
P BRS047 Breast Cancer 99 0.157
12
HPT019 Hepatic Encephalopathy 60 0.151
13
HPT004 Hepatic Coma 42 0.149
14
P NRB010 Neuroblastoma 1 66 0.147
15
P LTR001 Lateral Sclerosis 56 0.143
16
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.140
17
P LVR013 Liver Disease 71 0.140
18
LVR012 Liver Cirrhosis 67 0.126
19
P PRS040 Prostate Cancer 97 0.118
20
P HNT016 Huntington Disease 72 0.118
21
P PHC003 Pheochromocytoma 71 0.115
22
P MVM001 Movement Disease 63 0.115
23
P PRN023 Prion Disease 57 0.115
24
HMS001 Hemosiderosis 54 0.115
25
ADR040 Adrenal Gland Pheochromocytoma 51 0.115
26
P RRH023 Rare Hereditary Hemochromatosis 41 0.115
27
48X005 48,xyyy 37 0.115
28
CHL123 Chlamydia 60 0.110
29
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.110
30
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.107
31
NTR005 Nutritional Deficiency Disease 61 0.104
32
HYP266 Hypoxia 58 0.104
33
P OVR042 Ovarian Cancer 89 0.101
34
c HMC039 Hemochromatosis, Type 1 73 0.101
35
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.101
36
P HPT023 Hepatocellular Carcinoma 99 0.098
37
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.098
38
DRM006 Dermatitis 63 0.098
39
HRW001 Hair Whorl 36 0.098
40
P LNG032 Lung Cancer 99 0.094
41
ISC004 Ischemia 62 0.094
42
c DLT002 Dilated Cardiomyopathy 81 0.091
43
MLN008 Melanoma 68 0.091
44
P ADN016 Adenocarcinoma 65 0.091
45
P GLM045 Glioma 64 0.091
46
GLL048 Glial Tumor 48 0.091
47
P BNG032 Benign Mesothelioma 47 0.091
48
HLX001 Helix Syndrome 46 0.091
49
P ALZ034 Alzheimer Disease 90 0.087
50
ESP021 Esophageal Cancer 90 0.087
51
P GST053 Gastric Cancer 85 0.087
52
GLB002 Glioblastoma 74 0.087
53
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.087
54
GLB015 Glioblastoma Multiforme 60 0.087
55
P FBR017 Fibrosarcoma 57 0.087
56
P ESP024 Esophagitis 62 0.084
57
SQM006 Squamous Cell Carcinoma 60 0.084
58
GTR002 Goiter 54 0.084
59
P AST007 Astrocytoma 52 0.084
60
CRB004 Cerebral Artery Occlusion 38 0.084
61
SCR011 Scrapie 37 0.084
62
PPL052 Papillomatosis, Confluent and Reticulated 34 0.084
63
DYS031 Dystonia/parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease 10 0.084
64
SLC035 Slc39a14 Deficiency 9 0.084
65
P PNC035 Pancreatic Cancer 86 0.080
66
DFC004 Deficiency Anemia 77 0.080
67
P MYC007 Myocardial Infarction 74 0.080
68
ALC007 Alcohol Dependence 68 0.080
69
SPN186 Spinal Cord Injury 63 0.080
70
TRD006 Tardive Dyskinesia 58 0.080
71
AGN016 Aging 58 0.080
72
c ATR087 Atrial Standstill 1 76 0.076
73
BRN024 Bronchitis 70 0.076
74
HYP066 Hyperglycemia 63 0.076
75
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.076
76
P PLY018 Polycythemia 56 0.076
77
P HYP086 Hypothyroidism 70 0.071
78
LNG099 Lung Disease 62 0.071
79
P SZR006 Seizure Disorder 59 0.071
80
c MST023 Mesothelioma, Malignant 59 0.071
81
TLN003 Telangiectasis 53 0.071
82
BRN071 Brain Injury 51 0.071
83
BNR002 Bone Resorption Disease 51 0.071
84
MNN028 Mononeuropathy of the Median Nerve, Mild 41 0.071
85
c HYP716 Hypermanganesemia with Dystonia 1 34 0.071
86
P ATX030 Ataxia-Telangiectasia 83 0.067
87
SVR004 Severe Combined Immunodeficiency 74 0.067
88
P PSR002 Psoriasis 63 0.067
89
DPH001 Diphtheria 61 0.067
90
VSL002 Visual Epilepsy 58 0.067
91
EXT034 Extrinsic Allergic Alveolitis 58 0.067
92
P ALC033 Alcohol Use Disorder 58 0.067
93
P PNM006 Pneumoconiosis 55 0.067
94
OCL069 Ocular Motor Apraxia 53 0.067
95
PST011 Pustulosis of Palm and Sole 51 0.067
96
47X002 47,xyy 49 0.067
97
CYT002 Cytokine Deficiency 46 0.067
98
ANT018 Anthracosis 46 0.067
99
P CLR023 Colorectal Cancer 100 0.062
100
P LNG064 Lung Cancer Susceptibility 3 79 0.062
101
P EPL164 Epilepsy 73 0.062
102
HMN044 Human Immunodeficiency Virus Type 1 73 0.062
103
RCK004 Rickets 70 0.062
104
CNG034 Congestive Heart Failure 69 0.062
105
ATH013 Atherosclerosis Susceptibility 68 0.062
106
P DBT009 Diabetes Mellitus 66 0.062
107
PRT037 Pertussis 66 0.062
108
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.062
109
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.062
110
DPR016 Depression 64 0.062
111
LYM017 Lyme Disease 64 0.062
112
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.062
113
CLT003 Colitis 63 0.062
114
STT001 Status Epilepticus 61 0.062
115
P BCL017 B-Cell Lymphoma 61 0.062
116
CNT047 Contact Dermatitis 58 0.062
117
TRM010 Traumatic Brain Injury 54 0.062
118
NPH018 Nephrogenic Systemic Fibrosis 51 0.062
119
c PCH010 Pachyonychia Congenita 3 43 0.062
120
PSD088 Pseudobulbar Affect 37 0.062
121
c CNG498 Congenital Disorder of Glycosylation, Type Iin 34 0.062
123
P HRT032 Heart Disease 78 0.056
124
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.056
125
c HYP836 Hypercholesterolemia, Familial, 1 74 0.056
126
P ATS364 Autism 68 0.056
127
P DRM053 Dermatitis, Atopic 68 0.056
128
P MCR115 Microvascular Complications of Diabetes 5 67 0.056
129
P CRN018 Coronary Artery Anomaly 67 0.056
130
P SKN015 Skin Carcinoma 67 0.056
131
P MTR014 Motor Neuron Disease 66 0.056
132
P VSC007 Vascular Disease 65 0.056
133
c HPT001 Hepatitis C 62 0.056
134
P PNC044 Pancreatitis 61 0.056
135
MNT002 Mental Depression 60 0.056
136
P CRN300 Coronary Heart Disease 1 59 0.056
137
IRN001 Iron Deficiency Anemia 59 0.056
138
P END033 Endocarditis 58 0.056
139
P INF037 Inflammatory Bowel Disease 57 0.056
140
P NRP001 Neuropathy 57 0.056
141
PRM236 Primary Biliary Cholangitis 57 0.056
142
c MCR113 Microvascular Complications of Diabetes 3 55 0.056
143
P PRM006 Primary Biliary Cirrhosis 54 0.056
144
TXC002 Toxic Encephalopathy 54 0.056
145
LRN003 Learning Disability 51 0.056
146
BLR001 Biliary Atresia 51 0.056
147
c MCR120 Microvascular Complications of Diabetes 7 48 0.056
148
P PRC019 Precocious Puberty 48 0.056
149
HDN002 Head Injury 47 0.056
150
DWR001 Dwarfism 45 0.056
151
c PRM038 Primary Agammaglobulinemia 45 0.056
152
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.056
153
c MLG079 Malignant Pleural Mesothelioma 43 0.056
154
c MCR130 Microvascular Complications of Diabetes 6 42 0.056
155
c MCR133 Microvascular Complications of Diabetes 4 42 0.056
156
HVY002 Heavy Metal Poisoning 23 0.056
157
c LKM061 Leukemia, Acute Myeloid 84 0.050
158
AST005 Asthma 80 0.050
159
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.050
160
CRV035 Cervical Cancer 77 0.050
161
P KDN018 Kidney Disease 73 0.050
162
P PNM007 Pneumonia 71 0.050
163
P LYM118 Lymphoma 70 0.050
164
c ATS007 Autism Spectrum Disorder 69 0.050
165
P HPT021 Hepatitis 69 0.050
166
P MJR001 Major Depressive Disorder 69 0.050
167
P LKM002 Leukemia 69 0.050
168
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.050
169
HYP056 Hypoglycemia 68 0.050
170
PSY004 Psychotic Disorder 68 0.050
171
P NRV007 Nervous System Disease 68 0.050
172
P NSP012 Nasopharyngeal Carcinoma 67 0.050
173
SRC014 Sarcoma 67 0.050
174
BRR014 Barrett Esophagus 67 0.050
175
P FRD012 Friedreich Ataxia 1 65 0.050
176
SKN016 Skin Disease 64 0.050
177
LPD008 Lipid Metabolism Disorder 64 0.050
178
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.050
179
FTT001 Fatty Liver Disease 63 0.050
180
MDD011 Mood Disorder 62 0.050
181
P LPS004 Lupus Erythematosus 62 0.050
182
CRD223 Cardiac Arrhythmia 61 0.050
183
P MYL006 Myeloid Leukemia 61 0.050
184
INS001 Insulinoma 60 0.050
185
ADN018 Adenoma 60 0.050
186
P OPT006 Optic Nerve Disease 59 0.050
187
c ACT075 Acute Myocardial Infarction 59 0.050
188
P MTC069 Mitochondrial Disorders 57 0.050
189
c BNG091 Benign Chronic Pemphigus 56 0.050
190
HYP005 Hypokalemia 55 0.050
191
P PLY019 Polyneuropathy 55 0.050
192
PLM017 Pulmonary Alveolar Microlithiasis 54 0.050
193
SPP010 Suppressor of Tumorigenicity 3 54 0.050
194
KFR001 Kufor-Rakeb Syndrome 54 0.050
195
P TMP001 Temporal Lobe Epilepsy 53 0.050
196
c ACT134 Acute Liver Failure 53 0.050
197
CHR073 Choreatic Disease 52 0.050
198
DNT012 Dental Caries 52 0.050
199
P CHR345 Chronic Pain 52 0.050
200
ENT011 Enterocolitis 51 0.050
201
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.050
202
PRL019 Prolidase Deficiency 44 0.050
203
ANX004 Anoxia 44 0.050
204
GNT033 Genetic Prion Diseases 37 0.050
205
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.050
206
PLY150 Polykaryocytosis Inducer 31 0.050
207
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.050
208
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.050
209
c HYP713 Hypermanganesemia with Dystonia 2 25 0.050
210
c PRK008 Parkinson Disease Type 9 21 0.050
211
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.044
212
c HYP595 Hypertension, Essential 87 0.044
213
OST012 Osteoarthritis 80 0.044
214
PFF001 Pfeiffer Syndrome 79 0.044
215
P BLD134 Bladder Cancer 79 0.044
216
P SCH015 Schizophrenia 76 0.044
217
c HPT073 Hepatitis C Virus 74 0.044
218
P MLT020 Multiple Sclerosis 73 0.044
219
MSC157 Muscular Dystrophy, Duchenne Type 70 0.044
220
DWN001 Down Syndrome 70 0.044
221
WLS001 Wilson Disease 69 0.044
222
P PLM037 Pulmonary Hypertension 69 0.044
223
P DMN002 Dementia 68 0.044
224
P MSC005 Muscular Dystrophy 68 0.044
225
P ASP006 Aspergillosis 67 0.044
226
P MNN013 Meningitis 67 0.044
227
OST159 Osteogenic Sarcoma 67 0.044
228
P PLM036 Pulmonary Fibrosis 66 0.044
229
P PRS038 Personality Disorder 66 0.044
230
P PRD008 Periodontitis 66 0.044
231
IDP011 Idiopathic Interstitial Pneumonia 65 0.044
232
P PRP019 Peripheral Nervous System Disease 64 0.044
233
P ENC004 Encephalitis 64 0.044
234
TRN015 Transient Cerebral Ischemia 62 0.044
235
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.044
236
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.044
237
P CTR002 Cataract 62 0.044
238
EYD002 Eye Disease 59 0.044
239
c ACT210 Acute Respiratory Distress Syndrome 59 0.044
240
BLR008 Bilirubin Metabolic Disorder 58 0.044
241
BRN056 Bronchopulmonary Dysplasia 57 0.044
242
SPN035 Spindle Cell Sarcoma 57 0.044
243
BRN004 Brain Edema 57 0.044
244
ALL010 Allergic Contact Dermatitis 56 0.044
245
c CNT035 Central Nervous System Disease 56 0.044
246
MCS002 Mucositis 56 0.044
247
PHR003 Pharyngitis 56 0.044
248
PPL022 Papilloma 56 0.044
249
P ART021 Arteriosclerosis 56 0.044
250
P SBS003 Substance Abuse 56 0.044
251
MST005 Mastitis 55 0.044
252
P HYP076 Hyperthyroidism 55 0.044
253
P DRR001 Diarrhea 55 0.044
254
PLG002 Plague 54 0.044
255
CHR100 Chronic Ulcer of Skin 53 0.044
256
THY030 Thyroid Gland Disease 53 0.044
257
NNL006 Non-Alcoholic Steatohepatitis 53 0.044
258
OCL006 Ocular Hypertension 52 0.044
259
P THY032 Thyroiditis 52 0.044
260
OVR082 Overgrowth Syndrome 51 0.044
261
URM002 Uremia 50 0.044
262
P SHR001 Short Bowel Syndrome 50 0.044
263
SQM002 Squamous Cell Papilloma 49 0.044
264
LYM019 Lymphosarcoma 48 0.044
265
P MRC003 Mercury Poisoning 47 0.044
266
PPT001 Peptic Esophagitis 47 0.044
267
c MLG068 Malignant Glioma 46 0.044
268
KWS001 Kwashiorkor 46 0.044
269
SPC005 Speech Disorder 44 0.044
270
ORL015 Oral Squamous Cell Carcinoma 44 0.044
271
TNG009 Tongue Squamous Cell Carcinoma 44 0.044
272
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.044
273
CHP002 Chops Syndrome 41 0.044
274
BBN001 Bubonic Plague 40 0.044
275
HRN029 Hearing Loss, Noise-Induced 38 0.044
276
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 32 0.044
277
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.044
278
THY006 Thymus Lymphoma 19 0.044
279
c SYS001 Systemic Lupus Erythematosus 88 0.036
280
MYL069 Myeloma, Multiple 85 0.036
281
P OST002 Osteoporosis 79 0.036
282
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.036
283
P RSP003 Respiratory Failure 75 0.036
284
CRH001 Crohn's Disease 75 0.036
285
BRN028 Brain Cancer 75 0.036
286
ANX010 Anxiety 75 0.036
287
c SPN225 Spondyloarthropathy 1 74 0.036
288
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.036
289
P SRC025 Sarcoidosis 1 72 0.036
290
P AMY004 Amyloidosis 71 0.036
291
MLT157 Multiple System Atrophy 1 71 0.036
292
ACR007 Acromegaly 70 0.036
293
P SYS005 Systemic Scleroderma 68 0.036
294
c CHR684 Chronic Kidney Disease 68 0.036
295
P HYP061 Hypertrophic Cardiomyopathy 68 0.036
296
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.036
297
CNN005 Connective Tissue Disease 68 0.036
298
P GLM040 Glioma Susceptibility 1 68 0.036
299
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.036
300
CRT072 Creutzfeldt-Jakob Disease 67 0.036
301
P FLL037 Follicular Lymphoma 67 0.036
302
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.036
303
c SML038 Small Cell Cancer of the Lung 67 0.036
304
P HRP006 Herpes Simplex 66 0.036
305
DSS008 Disease of Mental Health 66 0.036
306
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.036
307
P NPH012 Nephrotic Syndrome 65 0.036
308
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.036
309
P NTR004 Neutropenia 64 0.036
310
c HPT016 Hepatitis B 63 0.036
311
c PRC016 Pre-Eclampsia 63 0.036
312
ACT119 Acute Promyelocytic Leukemia 63 0.036
313
P MYP004 Myopathy 63 0.036
314
TXC005 Toxic Shock Syndrome 63 0.036
315
ADL002 Adult Syndrome 62 0.036
316
BRC012 Brucellosis 62 0.036
317
TTN003 Tetanus 62 0.036
318
ATM095 Autoimmune Disease 62 0.036
319
P URT039 Urticaria 61 0.036
320
PRT013 Portal Hypertension 61 0.036
321
ACQ007 Acquired Immunodeficiency Syndrome 61 0.036
322
CHR066 Chronic Fatigue Syndrome 61 0.036
323
HLC007 Helicobacter Pylori Infection 61 0.036
324
P CRD132 Cardiac Conduction Defect 61 0.036
325
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.036
326
SPP011 Suppression of Tumorigenicity 12 61 0.036
327
CHL067 Cholecystitis 60 0.036
328
ALC006 Alcoholic Hepatitis 60 0.036
329
FBR047 Fibromyalgia 60 0.036
330
LGG001 Legg-Calve-Perthes Disease 60 0.036
331
GST045 Gastroenteritis 60 0.036
332
c HPT003 Hepatitis a 60 0.036
333
P INF032 Infertility 60 0.036
334
c DWL002 Dowling-Degos Disease 1 59 0.036
335
P RHN004 Rhinitis 59 0.036
336
P UVT001 Uveitis 58 0.036
337
P PLY011 Polycystic Ovary Syndrome 58 0.036
338
P MYP006 Myopia 58 0.036
339
NWB001 Newborn Respiratory Distress Syndrome 58 0.036
340
c ESS001 Essential Tremor 58 0.036
341
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.036
342
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.036
343
P GST044 Gastritis 58 0.036
344
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.036
345
P PLY041 Polymyositis 57 0.036
346
P GRV001 Graves' Disease 57 0.036
347
P MLN007 Male Infertility 57 0.036
348
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.036
349
ENH001 Enhanced S-Cone Syndrome 56 0.036
350
c VRL010 Viral Hepatitis 56 0.036
351
c SVR001 Severe Acute Respiratory Syndrome 56 0.036
352
P RTN016 Retinal Degeneration 56 0.036
353
PLM010 Pulmonary Edema 56 0.036
354
HYP060 Hyperinsulinism 55 0.036
355
PRN019 Perinatal Necrotizing Enterocolitis 55 0.036
356
PLM012 Pulmonary Sarcoidosis 54 0.036
357
P MYS005 Myositis 54 0.036
358
INF034 Infective Endocarditis 53 0.036
359
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.036
360
IMP005 Impotence 53 0.036
361
P LRY019 Laryngitis 53 0.036
362
NRT001 Neurotic Disorder 53 0.036
363
LNG031 Lung Benign Neoplasm 52 0.036
364
MYM001 Myoma 52 0.036
365
NRT004 Neuritis 52 0.036
366
c CRD185 Ceroid Lipofuscinosis, Neuronal, 6 52 0.036
367
STM007 Stomatitis 51 0.036
368
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.036
369
CLR109 Colorectal Adenocarcinoma 51 0.036
370
ISL003 Isolated Growth Hormone Deficiency 50 0.036
371
MTC005 Mitochondrial Metabolism Disease 50 0.036
372
c HNT010 Huntington Disease-Like 1 49 0.036
373
ATS010 Autosomal Recessive Disease 49 0.036
374
c HMC035 Hemochromatosis, Type 4 48 0.036
375
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.036
376
c BPL002 Bipolar I Disorder 48 0.036
377
LNG015 Lingual-Facial-Buccal Dyskinesia 48 0.036
378
c HNT004 Huntington Disease-Like 2 48 0.036
379
HYP017 Hypophosphatemia 48 0.036
380
GLC106 Glucocorticoid Resistance, Generalized 48 0.036
381
PRN009 Paranoid Schizophrenia 47 0.036
382
KRT002 Keratomalacia 47 0.036
383
MCR018 Microcytic Anemia 46 0.036
384
SYN036 Syncope 46 0.036
385
CCC002 Coccidiosis 46 0.036
386
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.036
387
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.036
388
BRN032 Brain Glioma 44 0.036
389
BLR013 Biliary Tract Cancer 44 0.036
390
DMP001 Dumping Syndrome 44 0.036
391
ASB001 Asbestosis 44 0.036
392
P HYP265 Hypotonia 43 0.036
393
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.036
394
ACT003 Acute Kidney Tubular Necrosis 42 0.036
395
ALL014 Allergic Encephalomyelitis 40 0.036
396
PNM005 Pneumonic Plague 40 0.036
397
CRD170 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1 40 0.036
399
c OVR114 Ovarian Cancer 1 39 0.036
400
c CNG383 Congenital Disorder of Glycosylation, Type Iik 37 0.036
401
END028 Endemic Goiter 37 0.036
402
ALC005 Alcoholic Pancreatitis 37 0.036
403
c CHR682 Chronic Bilirubin Encephalopathy 36 0.036
404
GNT167 Genetic Obesity 35 0.036
405
MLR009 Miliaria 35 0.036
406
CRR017 Curry-Jones Syndrome 35 0.036
407
PCD001 Pica Disease 33 0.036
408
MLR001 Miliaria Rubra 32 0.036
409
PST092 Posttransplant Acute Limbic Encephalitis 29 0.036
410
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.036
411
ASB003 Asbestos Intoxication 26 0.036
412
DRM046 Dermal Ridges-off-the-End 24 0.036
413
MLR026 Miliaria Crystallina 13 0.036
414
MRV001 Morvan's Fibrillary Chorea 13 0.036
415
NRL016 Neural Tube Defects 83 0.025
416
P RHM011 Rheumatoid Arthritis 82 0.025
417
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.025
418
IMM167 Immune Deficiency Disease 79 0.025
419
P MDL005 Medulloblastoma 78 0.025
420
P NRF023 Neurofibromatosis, Type Ii 77 0.025
421
GST019 Gastrointestinal Stromal Tumor 76 0.025
422
ULC004 Ulcerative Colitis 75 0.025
423
SCK003 Sickle Cell Anemia 74 0.025
424
P RTN024 Retinoblastoma 74 0.025
425
c LKM063 Leukemia, Chronic Myeloid 74 0.025
426
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.025
427
c TBR025 Tuberous Sclerosis 1 74 0.025
428
P TBR001 Tuberous Sclerosis 72 0.025
429
P CNR004 Cone-Rod Dystrophy 2 72 0.025
430
PLM001 Pulmonary Tuberculosis 72 0.025
431
OTT002 Otitis Media 71 0.025
432
P ART022 Arthritis 71 0.025
433
P SLP006 Sleep Apnea 71 0.025
434
P TTR001 Tetralogy of Fallot 70 0.025
435
LYM133 Lymphoma, Hodgkin, Classic 70 0.025
436
c EXD008 Exudative Vitreoretinopathy 1 69 0.025
437
P INF038 Influenza 69 0.025
438
LGH007 Leigh Syndrome 69 0.025
439
P CHR012 Chronic Granulomatous Disease 69 0.025
440
KRT019 Keratitis, Hereditary 69 0.025
441
PNC129 Pancreatic Adenocarcinoma 69 0.025
442
CMM004 Common Variable Immunodeficiency 69 0.025
443
OBS002 Obsessive-Compulsive Disorder 69 0.025
444
CHL065 Cholangiocarcinoma 68 0.025
445
GST092 Gastroesophageal Reflux 68 0.025
446
BRK010 Burkitt Lymphoma 68 0.025
447
c BSL007 Basal Cell Carcinoma 68 0.025
448
P LPR021 Leprosy 3 67 0.025
449
c HRD010 Hereditary Spastic Paraplegia 67 0.025
450
P HYP098 Hypereosinophilic Syndrome 67 0.025
451
P CNJ013 Conjunctivitis 67 0.025
452
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.025
453
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.025
454
GST040 Gastric Adenocarcinoma 67 0.025
455
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.025
456
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.025
457
AND002 Androgen Insensitivity Syndrome 66 0.025
458
CHG001 Chagas Disease 66 0.025
459
INC002 Inclusion Body Myositis 66 0.025
460
ANG054 Angina Pectoris 66 0.025
461
P TRN020 Turner Syndrome 66 0.025
462
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.025
463
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.025
464
P ANG001 Angelman Syndrome 65 0.025
465
MSC007 Muscle Hypertrophy 65 0.025
466
P CHR071 Charcot-Marie-Tooth Disease 65 0.025
467
IRR002 Irritable Bowel Syndrome 65 0.025
468
TBC004 Tobacco Addiction 65 0.025
469
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 64 0.025
470
CLR108 Colorectal Adenoma 64 0.025
471
ANR007 Anorexia Nervosa 64 0.025
472
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.025
473
P HML002 Hemolytic Anemia 64 0.025
474
P HYP069 Hyperparathyroidism 64 0.025
475
KRN002 Kearns-Sayre Syndrome 64 0.025
476
c RHB024 Rhabdomyosarcoma 2 64 0.025
477
HTC003 Hutchinson-Gilford Progeria Syndrome 64 0.025
478
P ANR048 Aniridia 1 64 0.025
479
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.025
480
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.025
481
c ACT068 Acute Cystitis 63 0.025
482
PSR001 Psoriatic Arthritis 63 0.025
483
P ACR001 Aicardi-Goutieres Syndrome 63 0.025
484
GLC006 Galactosemia 63 0.025
485
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.025
486
c BRN108 Branchiootic Syndrome 1 62 0.025
487
P LPS002 Liposarcoma 62 0.025
488
P HYP750 Hypertriglyceridemia, Familial 62 0.025
489
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.025
490
NRM005 Neuromuscular Disease 62 0.025
491
VRL011 Viral Infectious Disease 62 0.025
492
CTR172 Citrullinemia, Classic 62 0.025
493
ACN002 Acanthosis Nigricans 62 0.025
494
P DRM010 Dermatomyositis 62 0.025
495
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.025
496
P ALP009 Alopecia Areata 61 0.025
497
c PNS012 Paine Syndrome 61 0.025
498
WST001 West Syndrome 61 0.025
499
c LCL006 Localized Scleroderma 61 0.025
500
P MCH002 Machado-Joseph Disease 61 0.025
501
MSL001 Measles 61 0.025
502
IGR001 Ige Responsiveness, Atopic 61 0.025
503
P ADL010 Adult Respiratory Distress Syndrome 61 0.025
504
PRT058 Pure Autonomic Failure 60 0.025
505
c ACT027 Acute Pancreatitis 60 0.025
506
ART001 Arterial Tortuosity Syndrome 60 0.025
507
c ACT071 Acute Kidney Failure 60 0.025
508
PPT005 Peptic Ulcer Disease 60 0.025
509
P KDN017 Kidney Cancer 60 0.025
510
LPT001 Leptospirosis 60 0.025
511
ART140 Arteries, Anomalies of 60 0.025
512
BRN002 Bronchiolitis 60 0.025
513
END030 End Stage Renal Failure 60 0.025
514
P CYS018 Cystitis 59 0.025
515
GRD007 Grade Iii Astrocytoma 59 0.025
516
P BRS044 Breast Adenocarcinoma 59 0.025
517
CNS004 Constipation 59 0.025
518
P SYP003 Syphilis 59 0.025
519
c CHL119 Cholangitis, Primary Sclerosing 59 0.025
520
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 58 0.025
521
P PRP029 Porphyria 58 0.025
522
P ALP008 Alopecia 58 0.025
523
GST033 Gestational Diabetes 58 0.025
524
MCK005 Mckusick-Kaufman Syndrome 58 0.025
525
P AXN002 Axenfeld-Rieger Syndrome 58 0.025
526
RCT015 Reactive Arthritis 58 0.025
527
P PYL005 Pyelonephritis 58 0.025
528
TNS005 Tonsillitis 58 0.025
529
P TRC086 Trichohepatoenteric Syndrome 1 57 0.025
530
P DNG005 Dengue Virus 57 0.025
531
P STR020 Strabismus 57 0.025
532
BRN045 Brunner Syndrome 57 0.025
533
GST050 Gastrointestinal System Disease 57 0.025
534
DCT002 Ductal Carcinoma in Situ 57 0.025
535
VSC002 Vascular Dementia 57 0.025
536
ALL006 Allergic Asthma 56 0.025
537
P LYM031 Lymphocytic Leukemia 56 0.025
538
c BCT007 Bacterial Meningitis 56 0.025
539
P RBL001 Rubella 56 0.025
540
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.025
541
ATR057 Atrioventricular Block 56 0.025
542
P SHR029 Short Syndrome 56 0.025
543
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.025
544
DBT010 Diabetic Neuropathy 56 0.025
545
c PRD040 Periodontitis, Chronic 56 0.025
546
P EPD003 Epidermolysis Bullosa Simplex 55 0.025
547
SYN007 Synovitis 55 0.025
548
SLC006 Silicosis 55 0.025
549
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
550
END040 Endogenous Depression 55 0.025
551
ANN002 Anencephaly 55 0.025
552
P LCH002 Lichen Planus 55 0.025
553
GLC003 Glucose Intolerance 55 0.025
554
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.025
555
c AML044 Amelogenesis Imperfecta, Type Ig 55 0.025
556
MXD005 Mixed Connective Tissue Disease 55 0.025
557
P OPT009 Optic Neuritis 55 0.025
558
P INS002 in Situ Carcinoma 55 0.025
559
GNR004 Generalized Anxiety Disorder 55 0.025
560
INT079 Intrahepatic Cholangiocarcinoma 54 0.025
561
P EPD016 Epidermolysis Bullosa 54 0.025
562
PRP016 Paraplegia 54 0.025
563
P HML001 Hemolytic-Uremic Syndrome 54 0.025
564
CLR030 Clear Cell Renal Cell Carcinoma 54 0.025
565
PTH003 Pathologic Nystagmus 53 0.025
566
P PNC025 Panic Disorder 53 0.025
567
EXP004 Exophthalmos 53 0.025
568
VLV032 Vulva Cancer 53 0.025
569
P MYS079 Miyoshi Muscular Dystrophy 53 0.025
570
P CHL066 Cholangitis 53 0.025
571
FCL012 Facial Paralysis 53 0.025
572
P RTN018 Retinal Disease 53 0.025
573
SPN051 Spondylitis 53 0.025
574
P PTT006 Pituitary Adenoma 53 0.025
575
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.025
576
ALC009 Alcoholic Liver Cirrhosis 53 0.025
577
STT041 Stuttering 53 0.025
578
c CNG412 Congenital Disorder of Glycosylation, Type Ii 52 0.025
579
DYS073 Dysphagia 52 0.025
580
FRB001 Farber Lipogranulomatosis 52 0.025
581
LMY002 Leiomyoma 52 0.025
582
RTN003 Retinal Ischemia 52 0.025
583
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.025
584
RGH009 Right Atrial Isomerism 52 0.025
585
c SCN007 Secondary Hyperparathyroidism 52 0.025
586
P TRT010 Teratoma 52 0.025
587
MCL006 Macular Retinal Edema 52 0.025
588
KRT009 Keratosis 52 0.025
589
OST011 Osteomalacia 51 0.025
590
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.025
591
PLC008 Placenta Disease 51 0.025
592
MYL020 Myelomeningocele 51 0.025
593
ASP003 Aseptic Meningitis 51 0.025
594
CRY005 Cryptococcosis 51 0.025
595
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.025
596
c INH020 Inherited Metabolic Disorder 51 0.025
597
PST021 Postpartum Depression 51 0.025
598
CHR005 Chorioamnionitis 51 0.025
599
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.025
600
LMB062 Limb Ischemia 50 0.025
601
PRV004 Periventricular Leukomalacia 50 0.025
602
P AGG001 Aggressive Periodontitis 50 0.025
603
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.025
604
RYN005 Raynaud Phenomenon 50 0.025
605
PLR022 Pleural Disease 50 0.025
606
P ALL008 Allergic Bronchopulmonary Aspergillosis 50 0.025
607
ALL009 Allergic Conjunctivitis 50 0.025
608
P INT099 Intrahepatic Cholestasis of Pregnancy 50 0.025
609
PLR008 Pleurisy 50 0.025
610
MLK003 Melkersson-Rosenthal Syndrome 50 0.025
611
c INF145 Infantile Liver Failure Syndrome 1 50 0.025
612
CRD137 Cardiogenic Shock 50 0.025
613
SXL003 Sexual Disorder 49 0.025
614
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.025
615
NTR046 Neutrophil Migration 49 0.025
616
P BLR006 Biliary Tract Disease 49 0.025
617
c ACT078 Acute Porphyria 49 0.025
618
ANS011 Anus Cancer 49 0.025
619
DGN001 Degenerative Disc Disease 49 0.025
620
LPD009 Lipid Storage Disease 49 0.025
621
P OBS001 Obstructive Jaundice 49 0.025
622
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.025
623
THR013 Thoracic Outlet Syndrome 49 0.025
624
P END046 Endometritis 49 0.025
625
SPL018 Splenomegaly 48 0.025
626
MTB004 Metabolic Acidosis 48 0.025
627
P FNG006 Feingold Syndrome 1 48 0.025
628
HYP781 Hypoascorbemia 48 0.025
629
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.025
630
ATN005 Autonomic Dysfunction 48 0.025
631
P NGH001 Night Blindness 48 0.025
632
CCN002 Cocaine Abuse 48 0.025
633
GRW007 Growth Hormone Deficiency 48 0.025
634
CLS016 Clostridium Difficile Colitis 48 0.025
635
c ANT034 Anterior Uveitis 48 0.025
636
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.025
637
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.025
638
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.025
639
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.025
640
ESN015 Eosinophilic Fasciitis 48 0.025
641
PPL002 Papillary Carcinoma 47 0.025
642
WTH001 Withdrawal Disorder 47 0.025
643
P SCL009 Sclerosing Cholangitis 47 0.025
644
BRN014 Bronchopneumonia 47 0.025
645
ORL013 Oral Lichen Planus 47 0.025
646
MYL013 Myeloperoxidase Deficiency 47 0.025
647
VTM033 Vitamin K Deficiency Bleeding 47 0.025
648
c RBN022 Robinow Syndrome, Autosomal Recessive 1 47 0.025
649
P DNR001 Duane Retraction Syndrome 47 0.025
650
TTH006 Tooth Disease 47 0.025
651
ANT011 Antisocial Personality Disorder 47 0.025
652
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.025
653
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.025
654
c VRL012 Viral Meningitis 47 0.025
655
CLD007 Cold Agglutinin Disease 47 0.025
656
FSC004 Fasciitis 47 0.025
657
P MTH007 Methemoglobinemia 47 0.025
658
c LBR004 Leber Congenital Amaurosis 1 47 0.025
659
ART004 Aortic Atherosclerosis 47 0.025
660
DBT006 Diabetic Macular Edema 46 0.025
661
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.025
662
GRN017 Granulocytopenia 46 0.025
663
c FML008 Familial Retinoblastoma 46 0.025
664
SPC010 Speech and Communication Disorders 46 0.025
665
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.025
666
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.025
667
PRS063 Paresthesia 46 0.025
668
P SMK004 Smoking As a Quantitative Trait Locus 3 46 0.025
669
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.025
670
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.025
671
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.025
672
CTS011 Cutis Marmorata Telangiectatica Congenita 45 0.025
673
CRB025 Carbohydrate Metabolic Disorder 45 0.025
674
TND005 Tendinitis 45 0.025
675
CRV043 Cervical Dystonia 45 0.025
676
ANL017 Anal Squamous Cell Carcinoma 45 0.025
677
MLN014 Melnick-Needles Syndrome 44 0.025
678
PLR007 Pleural Empyema 44 0.025
679
INT052 Intestinal Volvulus 44 0.025
680
DSC009 Discoid Lupus Erythematosus 44 0.025
681
TND004 Tendinopathy 44 0.025
682
CTY001 Cat Eye Syndrome 44 0.025
683
IDP091 Idiopathic Nephrotic Syndrome 43 0.025
684
MTS001 Mutism 43 0.025
685
c PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 43 0.025
686
P AVS003 Avascular Necrosis 43 0.025
687
FLL031 Follicular Adenoma 43 0.025
688
SMN007 Seminoma 43 0.025
689
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.025
690
P CRB088 Cerebral Atrophy 43 0.025
691
c PRG039 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 43 0.025
692
CHL109 Childhood Apraxia of Speech 43 0.025
693
ESN002 Eosinophilia-Myalgia Syndrome 43 0.025
694
MDS022 Mediastinitis 42 0.025
695
VNZ002 Venezuelan Equine Encephalitis 42 0.025
696
LMB024 Limbic Encephalitis 42 0.025
697
ACT088 Acute Insulin Response 42 0.025
698
PRS042 Prostate Disease 42 0.025
699
ALC010 Alcoholic Cardiomyopathy 42 0.025
700
CRB033 Cerebral Degeneration 42 0.025
701
P SDR002 Siderosis 42 0.025
702
INT304 Interstitial Pneumonitis, Desquamative, Familial 42 0.025
703
PRM175 Primary Familial Brain Calcification 42 0.025
704
LTX001 Latex Allergy 42 0.025
705
CNV002 Conversion Disorder 42 0.025
706
FNG016 Fungal Keratitis 42 0.025
707
SPT002 Septicemic Plague 41 0.025
708
VST004 Vestibular Disease 41 0.025
709
CRV045 Cervical Intraepithelial Neoplasia 41 0.025
710
DRG002 Drug-Induced Hepatitis 41 0.025
711
SNL007 Senile Cataract 41 0.025
712
CNT060 Central Serous Chorioretinopathy 41 0.025
713
PRM329 Premature Aging 41 0.025
714
EXC002 Exocrine Pancreatic Insufficiency 41 0.025
715
PRT019 Protein-Losing Enteropathy 41 0.025
716
PLY100 Polyploidy 41 0.025
717
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 40 0.025
718
MYF001 Myofibroma 40 0.025
719
LKP003 Leukoplakia 40 0.025
720
MST004 Mast Cell Neoplasm 40 0.025
721
SLF014 Sulfite Oxidase Deficiency, Isolated 40 0.025
722
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.025
723
c MLG157 Malignant Pheochromocytoma 40 0.025
724
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 40 0.025
725
c DNR003 Duane Retraction Syndrome 1 40 0.025
726
MYF002 Myofascial Pain Syndrome 39 0.025
727
LWG005 Low-Grade Astrocytoma 39 0.025
728
OVR094 Ovarian Epithelial Cancer 39 0.025
729
PRD003 Periodontosis 39 0.025
730
MRS001 Marasmus 39 0.025
731
HYP264 Hypertonia 39 0.025
732
WCK001 Wieacker-Wolff Syndrome 39 0.025
733
CHL147 Chlamydia Pneumonia 39 0.025
734
ATX010 Ataxia Neuropathy Spectrum 39 0.025
735
RDT001 Radiation Cystitis 39 0.025
736
EXT007 Extracutaneous Mastocytoma 39 0.025
737
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 38 0.025
738
EPT021 Epithelial Recurrent Erosion Dystrophy 38 0.025
739
c PLY105 Polycystic Ovary Syndrome 1 38 0.025
740
HYP001 Hypochromic Microcytic Anemia 38 0.025
741
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 38 0.025
742
MYS001 Myositis Ossificans 38 0.025
743
URT014 Ureterolithiasis 38 0.025
744
c HNT011 Huntington Disease-Like 3 37 0.025
745
STR103 Streptococcus Pneumonia 37 0.025
746
SMT020 Smith-Kingsmore Syndrome 37 0.025
747
NTL004 Nut Allergy 37 0.025
748
NRN002 Neuronitis 37 0.025
749
TNS014 Tenosynovitis 37 0.025
750
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.025
751
END072 Endotheliitis 36 0.025
752
RNL012 Renal Tuberculosis 36 0.025
753
KLB003 Klebsiella Pneumonia 36 0.025
754
MXD026 Mixed Glioma 36 0.025
755
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.025
756
WBR001 Weber Syndrome 35 0.025
757
HNS001 Hansen's Disease 35 0.025
758
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 35 0.025
759
BLR028 Biliary Atresia, Extrahepatic 35 0.025
761
LYM043 Lymphocytic Hypophysitis 34 0.025
762
ANS025 Anus Benign Neoplasm 34 0.025
763
TLS001 Tolosa-Hunt Syndrome 34 0.025
764
ALL007 Allergic Urticaria 34 0.025
765
c MJR003 Major Affective Disorder 6 34 0.025
766
c MJR006 Major Affective Disorder 5 34 0.025
767
c SPS097 Spastic Paraplegia 13, Autosomal Dominant 34 0.025
768
c PLY136 Polydactyly, Preaxial I 34 0.025
769
NNS011 Nonseminomatous Germ Cell Tumor 33 0.025
770
CND006 Candida Glabrata 33 0.025
771
DYT006 Dyt-Tor1a 32 0.025
772
ALR002 Al-Raqad Syndrome 32 0.025
773
RCH002 Richards-Rundle Syndrome 32 0.025
774
c FBR070 Febrile Seizures, Familial, 8 31 0.025
775
CRB009 Cerebritis 31 0.025
776
MCH006 Mechanical Strabismus 31 0.025
777
ANP008 Anaplastic Oligoastrocytoma 31 0.025
778
c PRG019 Paragangliomas 2 30 0.025
779
OCC001 Occupational Dermatitis 30 0.025
780
MYC088 Mycobacterium Avium Complex Infections 30 0.025
781
CHR028 Chronic Wasting Disease 30 0.025
782
IMM162 Immunoglobulin E Concentration, Serum 29 0.025
783
c BLD140 Blood Group, I System 29 0.025
784
INF009 Inflammatory Spondylopathy 29 0.025
785
BLC012 Bile Acid Malabsorption, Primary 29 0.025
786
VST003 Vestibular Nystagmus 29 0.025
787
c ERL012 Early-Onset Glaucoma 29 0.025
788
c EPL200 Epilepsy, Childhood Absence 1 29 0.025
789
ARG004 Argyria 28 0.025
790
P ACT232 Acute Necrotizing Encephalopathy 28 0.025
791
MYP120 Myopathy, Distal, with Rimmed Vacuoles 28 0.025
792
MNG003 Mungan Syndrome 28 0.025
793
CHL079 Children's Interstitial Lung Disease 27 0.025
794
ACT162 Acute Sensory Ataxic Neuropathy 27 0.025
795
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 27 0.025
796
TXC004 Toxic Diffuse Goiter 27 0.025
797
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 27 0.025
798
c TTH010 Tooth Agenesis, Selective, 1 26 0.025
799
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.025
800
PTN004 Patent Ductus Venosus 26 0.025
801
MTH071 Methane Production 26 0.025
802
DFN341 Deafness, Unilateral 25 0.025
803
ADG002 Audiogenic Seizures 25 0.025
804
BLD163 Blood Group, Dombrock System 24 0.025
805
CYN003 Cyanide Poisoning 24 0.025
806
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 24 0.025
807
SDD004 Sudden Arrhythmia Death Syndrome 23 0.025
808
MSL005 Mseleni Joint Disease 21 0.025
809
c SPS023 Spastic Paraplegia 13 21 0.025
810
DSS012 Disseminated Infection with Mycobacterium Avium Complex 21 0.025
811
CRN311 Coronary Ostial Stenosis or Atresia 20 0.025
812
PYT001 Pythiosis 20 0.025
813
MLS013 Miles-Carpenter Syndrome 20 0.025
814
AND005 Androgen Insensitivity Syndrome, Mild 20 0.025
815
c AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 19 0.025
816
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.025
817
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 18 0.025
818
CNG491 Congenital Portosystemic Shunt 17 0.025
819
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 17 0.025
820
BLD137 Blood Group--Ahonen 17 0.025
821
LTH004 Lathyrism 16 0.025
822
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 14 0.025
823
HND010 Handigodu Disease 13 0.025
824
c SPN403 Spinocerebellar Ataxia, X-Linked 2 13 0.025
825
RFR006 Refractory Cytopenia with Unilineage Dysplasia 12 0.025
826
P CRB180 Cerebelloparenchymal Disorder Ii 12 0.025
Content
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