Search results for Manganese

842 hits were found for Manganese

# Family MCID Name MIFTS Score
1
MNG007 Manganese Poisoning 29 5.383
2
P HYP821 Hypermanganesemia with Dystonia 26 2.665
3
DSR032 Disorder of Manganese Transport 6 2.627
4
P TRM003 Tremor 54 0.202
5
IRN002 Iron Metabolism Disease 57 0.195
6
P ENC018 Encephalopathy 61 0.184
7
P PRK057 Parkinson Disease, Late-Onset 78 0.182
8
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.180
9
CHL068 Cholestasis 61 0.175
10
P DYS154 Dystonia 65 0.165
11
P BRS047 Breast Cancer 97 0.153
12
P NRB001 Neuroblastoma 72 0.147
13
HPT019 Hepatic Encephalopathy 60 0.147
14
HPT004 Hepatic Coma 45 0.145
15
P LTR001 Lateral Sclerosis 54 0.139
16
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.137
17
P LVR013 Liver Disease 68 0.130
18
P HNT016 Huntington Disease 72 0.125
19
P PRS040 Prostate Cancer 97 0.120
20
P MVM001 Movement Disease 63 0.118
21
P PHC003 Pheochromocytoma 71 0.115
22
LVR012 Liver Cirrhosis 62 0.115
23
HMS001 Hemosiderosis 54 0.115
24
ADR040 Adrenal Gland Pheochromocytoma 46 0.115
25
P RRH023 Rare Hereditary Hemochromatosis 41 0.115
26
P PRN023 Prion Disease 57 0.113
27
48X005 48,xyyy 39 0.113
28
NTR005 Nutritional Deficiency Disease 62 0.107
29
CHL123 Chlamydia 59 0.107
30
HYP266 Hypoxia 57 0.107
31
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.107
32
P HPT023 Hepatocellular Carcinoma 100 0.101
33
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.101
34
P OVR042 Ovarian Cancer 88 0.098
35
HRW001 Hair Whorl 36 0.098
36
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.095
37
c HMC039 Hemochromatosis, Type 1 74 0.095
38
ISC004 Ischemia 58 0.095
39
DRM006 Dermatitis 61 0.092
40
P ALZ034 Alzheimer Disease 88 0.089
41
c DLT002 Dilated Cardiomyopathy 79 0.089
42
GLB015 Glioblastoma Multiforme 75 0.089
43
P MLN008 Melanoma 69 0.089
44
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.089
45
P ADN016 Adenocarcinoma 64 0.089
46
HLX001 Helix Syndrome 47 0.089
47
P BNG032 Benign Mesothelioma 46 0.089
48
P LNG032 Lung Cancer 98 0.085
49
ESP021 Esophageal Cancer 90 0.085
50
P GST053 Gastric Cancer 83 0.085
51
SQM006 Squamous Cell Carcinoma 60 0.085
52
P FBR017 Fibrosarcoma 56 0.085
53
P GLM045 Glioma 63 0.081
54
P ESP024 Esophagitis 62 0.081
55
SPN186 Spinal Cord Injury 60 0.081
56
P PLY018 Polycythemia 56 0.081
57
GTR002 Goiter 53 0.081
58
P AST007 Astrocytoma 51 0.081
59
GLL048 Glial Tumor 45 0.081
60
CRB004 Cerebral Artery Occlusion 45 0.081
61
SCR011 Scrapie 39 0.081
62
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.081
63
PPL052 Papillomatosis, Confluent and Reticulated 33 0.081
64
DYS031 Dystonia/parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease 9 0.081
65
SLC035 Slc39a14 Deficiency 9 0.081
66
P PNC035 Pancreatic Cancer 84 0.078
67
P MYC007 Myocardial Infarction 70 0.078
68
DFC004 Deficiency Anemia 70 0.078
69
ALC007 Alcohol Dependence 66 0.078
70
HYP066 Hyperglycemia 61 0.078
71
TRD006 Tardive Dyskinesia 54 0.078
72
c ATR087 Atrial Standstill 1 75 0.074
73
BRN024 Bronchitis 68 0.074
74
DPH001 Diphtheria 60 0.074
75
KFR001 Kufor-Rakeb Syndrome 60 0.074
76
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.074
77
P EPL164 Epilepsy 71 0.069
78
P HYP086 Hypothyroidism 69 0.069
79
c MST023 Mesothelioma, Malignant 57 0.069
80
AGN016 Aging 56 0.069
81
TLN003 Telangiectasis 52 0.069
82
47X002 47,xyy 49 0.069
83
BRN071 Brain Injury 49 0.069
84
BNR002 Bone Resorption Disease 48 0.069
85
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.069
86
c HYP716 Hypermanganesemia with Dystonia 1 35 0.069
87
P ATX030 Ataxia-Telangiectasia 82 0.065
88
SVR004 Severe Combined Immunodeficiency 73 0.065
89
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.065
90
CLT003 Colitis 62 0.065
91
P PSR002 Psoriasis 62 0.065
92
LNG099 Lung Disease 60 0.065
93
P ALC033 Alcohol Use Disorder 58 0.065
94
EXT034 Extrinsic Allergic Alveolitis 58 0.065
95
P SZR006 Seizure Disorder 56 0.065
96
P PNM006 Pneumoconiosis 56 0.065
97
PST011 Pustulosis of Palm and Sole 52 0.065
98
ANT018 Anthracosis 48 0.065
99
CYT002 Cytokine Deficiency 42 0.065
100
P CLR023 Colorectal Cancer 99 0.060
101
P LNG064 Lung Cancer Susceptibility 3 78 0.060
102
HMN044 Human Immunodeficiency Virus Type 1 71 0.060
103
P ATS364 Autism 70 0.060
104
CNG034 Congestive Heart Failure 69 0.060
105
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.060
106
RCK004 Rickets 68 0.060
107
PRT037 Pertussis 65 0.060
108
ATH013 Atherosclerosis Susceptibility 65 0.060
109
LYM017 Lyme Disease 64 0.060
110
DPR016 Depression 63 0.060
111
STT001 Status Epilepticus 60 0.060
112
VSL002 Visual Epilepsy 59 0.060
113
P BCL017 B-Cell Lymphoma 58 0.060
114
CNT047 Contact Dermatitis 58 0.060
115
DNT012 Dental Caries 53 0.060
116
OCL069 Ocular Motor Apraxia 51 0.060
117
NPH018 Nephrogenic Systemic Fibrosis 50 0.060
118
P PRC019 Precocious Puberty 46 0.060
119
P CHR345 Chronic Pain 44 0.060
120
c PCH010 Pachyonychia Congenita 3 44 0.060
121
c CNG498 Congenital Disorder of Glycosylation, Type Iin 40 0.060
122
PSD088 Pseudobulbar Affect 36 0.060
124
P GLM040 Glioma Susceptibility 1 81 0.055
125
P HRT032 Heart Disease 75 0.055
126
c HYP836 Hypercholesterolemia, Familial, 1 73 0.055
127
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.055
128
P PNM007 Pneumonia 68 0.055
129
P HPT021 Hepatitis 67 0.055
130
c ATS007 Autism Spectrum Disorder 67 0.055
131
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.055
132
P SKN015 Skin Carcinoma 66 0.055
133
P MCR115 Microvascular Complications of Diabetes 5 66 0.055
134
P DRM053 Dermatitis, Atopic 66 0.055
135
P MTR014 Motor Neuron Disease 65 0.055
136
P VSC007 Vascular Disease 63 0.055
137
P CRN300 Coronary Heart Disease 1 63 0.055
138
c HPT001 Hepatitis C 62 0.055
139
LPP008 Lipoprotein Quantitative Trait Locus 62 0.055
140
P PRM006 Primary Biliary Cirrhosis 62 0.055
141
FTT001 Fatty Liver Disease 61 0.055
142
P PNC044 Pancreatitis 61 0.055
143
INS001 Insulinoma 60 0.055
144
P OPT006 Optic Nerve Disease 60 0.055
145
IRN001 Iron Deficiency Anemia 59 0.055
146
MNT002 Mental Depression 58 0.055
147
P END033 Endocarditis 57 0.055
148
P CRD246 Cardiovascular System Disease 57 0.055
149
P NRP001 Neuropathy 56 0.055
150
P INF037 Inflammatory Bowel Disease 54 0.055
151
TXC002 Toxic Encephalopathy 53 0.055
152
c MCR113 Microvascular Complications of Diabetes 3 52 0.055
153
TRM010 Traumatic Brain Injury 51 0.055
154
BLR001 Biliary Atresia 50 0.055
155
LRN003 Learning Disability 49 0.055
156
c MCR120 Microvascular Complications of Diabetes 7 47 0.055
157
HDN002 Head Injury 46 0.055
158
DWR001 Dwarfism 44 0.055
159
c PRM038 Primary Agammaglobulinemia 44 0.055
160
c MLG079 Malignant Pleural Mesothelioma 42 0.055
161
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.055
162
c MCR130 Microvascular Complications of Diabetes 6 41 0.055
163
c MCR133 Microvascular Complications of Diabetes 4 41 0.055
164
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.055
165
HVY002 Heavy Metal Poisoning 22 0.055
166
c LKM061 Leukemia, Acute Myeloid 84 0.049
167
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.049
168
AST005 Asthma 76 0.049
169
P KDN018 Kidney Disease 72 0.049
170
P LYM118 Lymphoma 68 0.049
171
P LKM002 Leukemia 68 0.049
172
P MJR001 Major Depressive Disorder 68 0.049
173
PSY004 Psychotic Disorder 67 0.049
174
P NSP012 Nasopharyngeal Carcinoma 66 0.049
175
HYP056 Hypoglycemia 66 0.049
176
P NRV007 Nervous System Disease 66 0.049
177
BRR014 Barrett Esophagus 65 0.049
178
c DBT099 Diabetes Mellitus, Type I 65 0.049
179
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.049
180
P FRD001 Friedreich Ataxia 64 0.049
181
SKN016 Skin Disease 63 0.049
182
LPD008 Lipid Metabolism Disorder 62 0.049
183
MDD011 Mood Disorder 62 0.049
184
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.049
185
P LPS004 Lupus Erythematosus 61 0.049
186
CRD223 Cardiac Arrhythmia 60 0.049
187
ADN018 Adenoma 59 0.049
188
c BNG091 Benign Chronic Pemphigus 58 0.049
189
c ACT075 Acute Myocardial Infarction 57 0.049
190
c ACT134 Acute Liver Failure 56 0.049
191
P MTC069 Mitochondrial Disorders 56 0.049
192
MCS002 Mucositis 56 0.049
193
P PLY019 Polyneuropathy 56 0.049
194
HYP005 Hypokalemia 55 0.049
195
P DRR001 Diarrhea 55 0.049
196
NNL006 Non-Alcoholic Steatohepatitis 54 0.049
197
INF034 Infective Endocarditis 53 0.049
198
CHR073 Choreatic Disease 52 0.049
199
PRL019 Prolidase Deficiency 52 0.049
200
P SPP010 Suppressor of Tumorigenicity 3 51 0.049
201
ENT011 Enterocolitis 51 0.049
202
STM007 Stomatitis 50 0.049
203
P TMP001 Temporal Lobe Epilepsy 50 0.049
204
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.049
205
ANX004 Anoxia 40 0.049
206
c HYP713 Hypermanganesemia with Dystonia 2 35 0.049
207
PLY150 Polykaryocytosis Inducer 31 0.049
208
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 30 0.049
209
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.049
210
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.049
211
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.043
212
c HYP595 Hypertension, Essential 84 0.043
213
PFF001 Pfeiffer Syndrome 79 0.043
214
OST012 Osteoarthritis 78 0.043
215
CRV035 Cervical Cancer 76 0.043
216
P SCH015 Schizophrenia 74 0.043
217
MSC157 Muscular Dystrophy, Duchenne Type 72 0.043
218
P MLT020 Multiple Sclerosis 72 0.043
219
c HPT073 Hepatitis C Virus 72 0.043
220
WLS001 Wilson Disease 71 0.043
221
DWN001 Down Syndrome 70 0.043
222
CRT072 Creutzfeldt-Jakob Disease 70 0.043
223
P ASP006 Aspergillosis 69 0.043
224
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.043
225
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.043
226
P PLM037 Pulmonary Hypertension 67 0.043
227
OST159 Osteogenic Sarcoma 66 0.043
228
P DMN002 Dementia 66 0.043
229
P MSC005 Muscular Dystrophy 66 0.043
230
P MNN013 Meningitis 66 0.043
231
P PLM036 Pulmonary Fibrosis 65 0.043
232
SRC014 Sarcoma 65 0.043
233
P PRS038 Personality Disorder 65 0.043
234
P DBT009 Diabetes Mellitus 64 0.043
235
P PRD008 Periodontitis 64 0.043
236
PLG002 Plague 63 0.043
237
TRN015 Transient Cerebral Ischemia 63 0.043
238
c SVR001 Severe Acute Respiratory Syndrome 62 0.043
239
P ENC004 Encephalitis 61 0.043
240
P MYL006 Myeloid Leukemia 60 0.043
241
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.043
242
P CTR002 Cataract 60 0.043
243
GST045 Gastroenteritis 59 0.043
244
EYD002 Eye Disease 58 0.043
245
P PRP019 Peripheral Nervous System Disease 58 0.043
246
P INF032 Infertility 57 0.043
247
BRN056 Bronchopulmonary Dysplasia 57 0.043
248
BLR008 Bilirubin Metabolic Disorder 57 0.043
249
PHR003 Pharyngitis 57 0.043
250
ALL010 Allergic Contact Dermatitis 56 0.043
251
BRN004 Brain Edema 56 0.043
252
CHR100 Chronic Ulcer of Skin 55 0.043
253
P SBS003 Substance Abuse 55 0.043
254
P HYP076 Hyperthyroidism 55 0.043
255
P ART021 Arteriosclerosis 54 0.043
256
PPL022 Papilloma 54 0.043
257
OCL006 Ocular Hypertension 53 0.043
258
MST005 Mastitis 53 0.043
259
P SHR001 Short Bowel Syndrome 53 0.043
260
c CNT035 Central Nervous System Disease 52 0.043
261
THY030 Thyroid Gland Disease 52 0.043
262
P THY032 Thyroiditis 52 0.043
263
PPT001 Peptic Esophagitis 52 0.043
264
CCC002 Coccidiosis 51 0.043
265
P OVR082 Overgrowth Syndrome 50 0.043
266
URM002 Uremia 49 0.043
267
P MRC003 Mercury Poisoning 48 0.043
268
LYM019 Lymphosarcoma 46 0.043
269
SQM002 Squamous Cell Papilloma 46 0.043
270
c MLG068 Malignant Glioma 46 0.043
271
CHP002 Chops Syndrome 44 0.043
272
KWS001 Kwashiorkor 44 0.043
273
TNG009 Tongue Squamous Cell Carcinoma 44 0.043
274
SPC005 Speech Disorder 43 0.043
275
ORL015 Oral Squamous Cell Carcinoma 43 0.043
276
BBN001 Bubonic Plague 41 0.043
277
HRN029 Hearing Loss, Noise-Induced 37 0.043
278
PST092 Posttransplant Acute Limbic Encephalitis 29 0.043
279
THY006 Thymus Lymphoma 26 0.043
280
c SYS001 Systemic Lupus Erythematosus 86 0.035
281
MYL069 Myeloma, Multiple 85 0.035
282
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.035
283
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.035
284
P RSP003 Respiratory Failure 74 0.035
285
BRN028 Brain Cancer 74 0.035
286
P OST002 Osteoporosis 74 0.035
287
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.035
288
CRH001 Crohn's Disease 74 0.035
289
c SPN225 Spondyloarthropathy 1 73 0.035
290
P CNR004 Cone-Rod Dystrophy 2 73 0.035
291
ANX010 Anxiety 73 0.035
292
ACR007 Acromegaly 71 0.035
293
P SRC025 Sarcoidosis 1 70 0.035
294
P AMY004 Amyloidosis 70 0.035
295
MLT157 Multiple System Atrophy 1 70 0.035
296
P HYP061 Hypertrophic Cardiomyopathy 70 0.035
297
c CHR684 Chronic Kidney Disease 70 0.035
298
P MYP004 Myopathy 70 0.035
299
P SYS005 Systemic Scleroderma 68 0.035
300
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.035
301
CNN005 Connective Tissue Disease 68 0.035
302
P FLL037 Follicular Lymphoma 67 0.035
303
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.035
304
c SML038 Small Cell Cancer of the Lung 65 0.035
305
TTN003 Tetanus 65 0.035
306
P HRP006 Herpes Simplex 65 0.035
307
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.035
308
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.035
309
BRC012 Brucellosis 64 0.035
310
c PRC016 Pre-Eclampsia 63 0.035
311
P NTR004 Neutropenia 63 0.035
312
ACT119 Acute Promyelocytic Leukemia 63 0.035
313
c HPT003 Hepatitis a 62 0.035
314
ATM095 Autoimmune Disease 62 0.035
315
TXC005 Toxic Shock Syndrome 62 0.035
316
ALC006 Alcoholic Hepatitis 61 0.035
317
CHR066 Chronic Fatigue Syndrome 61 0.035
318
VRL011 Viral Infectious Disease 61 0.035
319
P NPH012 Nephrotic Syndrome 60 0.035
320
ACQ007 Acquired Immunodeficiency Syndrome 60 0.035
321
LGG001 Legg-Calve-Perthes Disease 60 0.035
322
c ACT071 Acute Kidney Failure 60 0.035
323
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.035
324
SPP011 Suppression of Tumorigenicity 12 59 0.035
325
PRT013 Portal Hypertension 59 0.035
326
c HPT016 Hepatitis B 59 0.035
327
P SLP005 Sleep Disorder 59 0.035
328
PRN019 Perinatal Necrotizing Enterocolitis 59 0.035
329
HLC007 Helicobacter Pylori Infection 59 0.035
330
FBR047 Fibromyalgia 58 0.035
331
CRD132 Cardiac Conduction Defect 58 0.035
332
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.035
333
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.035
334
P URT039 Urticaria 58 0.035
335
NWB001 Newborn Respiratory Distress Syndrome 58 0.035
336
c DWL002 Dowling-Degos Disease 1 58 0.035
337
P UVT001 Uveitis 57 0.035
338
CHL067 Cholecystitis 57 0.035
339
P PLY041 Polymyositis 57 0.035
340
P RHN004 Rhinitis 57 0.035
341
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.035
342
P MYS005 Myositis 56 0.035
343
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.035
344
P PLY011 Polycystic Ovary Syndrome 56 0.035
345
c ESS001 Essential Tremor 56 0.035
346
BCT022 Bacterial Infectious Disease 56 0.035
347
P GST044 Gastritis 56 0.035
348
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.035
349
P MLN007 Male Infertility 55 0.035
350
P GRV001 Graves' Disease 55 0.035
351
P MYP006 Myopia 55 0.035
352
HYP060 Hyperinsulinism 54 0.035
353
AMN003 Amnestic Disorder 54 0.035
354
PLM010 Pulmonary Edema 54 0.035
355
MYM001 Myoma 54 0.035
356
PLM012 Pulmonary Sarcoidosis 53 0.035
357
c HNT010 Huntington Disease-Like 1 53 0.035
358
P RTN016 Retinal Degeneration 53 0.035
359
SPN035 Spindle Cell Sarcoma 53 0.035
360
NRT001 Neurotic Disorder 53 0.035
361
P LRY019 Laryngitis 52 0.035
362
c VRL010 Viral Hepatitis 52 0.035
363
NRT004 Neuritis 52 0.035
364
IMP005 Impotence 52 0.035
365
CLR109 Colorectal Adenocarcinoma 51 0.035
366
LNG031 Lung Benign Neoplasm 51 0.035
367
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.035
368
PNM005 Pneumonic Plague 51 0.035
369
c HNT004 Huntington Disease-Like 2 50 0.035
370
PST021 Postpartum Depression 50 0.035
371
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.035
372
PRN009 Paranoid Schizophrenia 50 0.035
373
HYP017 Hypophosphatemia 50 0.035
374
ISL003 Isolated Growth Hormone Deficiency 49 0.035
375
MTC005 Mitochondrial Metabolism Disease 49 0.035
376
c BPL002 Bipolar I Disorder 49 0.035
377
ATS010 Autosomal Recessive Disease 48 0.035
378
GLC106 Glucocorticoid Resistance, Generalized 48 0.035
379
MCR018 Microcytic Anemia 47 0.035
380
ASB001 Asbestosis 47 0.035
381
KRT002 Keratomalacia 47 0.035
382
SYN036 Syncope 45 0.035
383
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.035
384
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.035
385
URL001 Urolithiasis 45 0.035
386
ACT003 Acute Kidney Tubular Necrosis 45 0.035
387
BRN032 Brain Glioma 45 0.035
388
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.035
389
DMP001 Dumping Syndrome 44 0.035
390
c CNG383 Congenital Disorder of Glycosylation, Type Iik 44 0.035
391
P HYP265 Hypotonia 43 0.035
392
BLR013 Biliary Tract Cancer 42 0.035
394
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.035
395
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.035
396
PCD001 Pica Disease 41 0.035
397
ALC005 Alcoholic Pancreatitis 40 0.035
398
c CHR682 Chronic Bilirubin Encephalopathy 39 0.035
399
ALL014 Allergic Encephalomyelitis 38 0.035
400
c OVR114 Ovarian Cancer 1 38 0.035
401
END028 Endemic Goiter 37 0.035
402
CRR017 Curry-Jones Syndrome 37 0.035
403
MLR009 Miliaria 34 0.035
404
MLR001 Miliaria Rubra 34 0.035
405
GNT167 Genetic Obesity 33 0.035
406
ASB003 Asbestos Intoxication 26 0.035
407
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.035
408
DRM046 Dermal Ridges-off-the-End 24 0.035
409
MLR026 Miliaria Crystallina 21 0.035
410
PRR015 Preauricular Fistulae, Congenital 20 0.035
411
MRV001 Morvan's Fibrillary Chorea 12 0.035
412
NRL016 Neural Tube Defects 82 0.025
413
c NRF023 Neurofibromatosis, Type Ii 80 0.025
414
P BLD134 Bladder Cancer 79 0.025
415
IMM167 Immune Deficiency Disease 78 0.025
416
GST019 Gastrointestinal Stromal Tumor 78 0.025
417
P MDL005 Medulloblastoma 77 0.025
418
c TBR025 Tuberous Sclerosis 1 77 0.025
419
SCK003 Sickle Cell Anemia 74 0.025
420
c BTT014 Beta-Thalassemia 74 0.025
421
ULC004 Ulcerative Colitis 73 0.025
422
P RTN024 Retinoblastoma 73 0.025
423
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.025
424
OTT002 Otitis Media 72 0.025
425
c EXD008 Exudative Vitreoretinopathy 1 71 0.025
426
GST040 Gastric Adenocarcinoma 70 0.025
427
LGH007 Leigh Syndrome 70 0.025
428
P TTR001 Tetralogy of Fallot 70 0.025
429
ADL002 Adult Syndrome 70 0.025
430
P TBR001 Tuberous Sclerosis 70 0.025
431
PLM001 Pulmonary Tuberculosis 69 0.025
432
P ART022 Arthritis 69 0.025
433
P SLP006 Sleep Apnea 69 0.025
434
LYM133 Lymphoma, Hodgkin, Classic 69 0.025
435
P LPR021 Leprosy 3 69 0.025
436
P ANG001 Angelman Syndrome 69 0.025
437
CHL065 Cholangiocarcinoma 68 0.025
438
CMM004 Common Variable Immunodeficiency 68 0.025
439
c BSL007 Basal Cell Carcinoma 68 0.025
440
OBS002 Obsessive-Compulsive Disorder 68 0.025
441
PCK003 Pick Disease of Brain 68 0.025
442
P INF038 Influenza 68 0.025
443
P FRN006 Frontotemporal Dementia 68 0.025
444
PNC129 Pancreatic Adenocarcinoma 68 0.025
445
GST092 Gastroesophageal Reflux 67 0.025
446
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.025
447
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.025
448
BRK010 Burkitt Lymphoma 67 0.025
449
P CHR012 Chronic Granulomatous Disease 67 0.025
450
P TRN020 Turner Syndrome 67 0.025
451
P HYP098 Hypereosinophilic Syndrome 67 0.025
452
c RHB024 Rhabdomyosarcoma 2 67 0.025
453
LPT001 Leptospirosis 66 0.025
454
ANG054 Angina Pectoris 66 0.025
455
ART001 Arterial Tortuosity Syndrome 66 0.025
456
c HRD010 Hereditary Spastic Paraplegia 66 0.025
457
AND002 Androgen Insensitivity Syndrome 66 0.025
458
CHG001 Chagas Disease 66 0.025
459
KHL003 Kohlschutter-Tonz Syndrome 65 0.025
460
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.025
461
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.025
462
P CNJ013 Conjunctivitis 65 0.025
463
KRT019 Keratitis, Hereditary 65 0.025
464
P LPS002 Liposarcoma 65 0.025
465
IRR002 Irritable Bowel Syndrome 65 0.025
466
P ADL010 Adult Respiratory Distress Syndrome 65 0.025
467
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.025
468
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.025
469
P CHR071 Charcot-Marie-Tooth Disease 65 0.025
470
NRM005 Neuromuscular Disease 64 0.025
471
TBC004 Tobacco Addiction 64 0.025
472
CTR172 Citrullinemia, Classic 64 0.025
473
P GLC113 Galactosemia I 64 0.025
474
CLR108 Colorectal Adenoma 64 0.025
475
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.025
476
MSC007 Muscle Hypertrophy 64 0.025
477
KRN002 Kearns-Sayre Syndrome 63 0.025
478
P HML002 Hemolytic Anemia 63 0.025
479
P ANR048 Aniridia 1 63 0.025
480
P HYP069 Hyperparathyroidism 63 0.025
481
c MLG084 Malignant Fibrous Histiocytoma 63 0.025
482
P SHR029 Short Syndrome 63 0.025
483
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.025
484
c ACT068 Acute Cystitis 63 0.025
485
ANR007 Anorexia Nervosa 63 0.025
486
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.025
487
c LCL006 Localized Scleroderma 62 0.025
488
c FNC043 Fanconi Anemia, Complementation Group E 62 0.025
489
P MCH002 Machado-Joseph Disease 62 0.025
490
c BRN108 Branchiootic Syndrome 1 62 0.025
491
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.025
492
P HYP750 Hypertriglyceridemia, Familial 62 0.025
493
P TRC086 Trichohepatoenteric Syndrome 1 62 0.025
494
P ACR001 Aicardi-Goutieres Syndrome 62 0.025
495
MSL001 Measles 62 0.025
496
P PRP029 Porphyria 62 0.025
497
P DRM010 Dermatomyositis 61 0.025
498
PSR001 Psoriatic Arthritis 61 0.025
499
MCK005 Mckusick-Kaufman Syndrome 61 0.025
500
c PNS012 Paine Syndrome 61 0.025
501
WST001 West Syndrome 61 0.025
502
RCT015 Reactive Arthritis 61 0.025
503
P KDN017 Kidney Cancer 60 0.025
504
RGH009 Right Atrial Isomerism 60 0.025
505
c ACT027 Acute Pancreatitis 60 0.025
506
ACN002 Acanthosis Nigricans 60 0.025
507
P ALP009 Alopecia Areata 60 0.025
508
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.025
509
ETN001 Eating Disorder 60 0.025
510
P THL005 Thalassemia 60 0.025
511
P RBL001 Rubella 59 0.025
512
P AXN002 Axenfeld-Rieger Syndrome 59 0.025
513
CHL014 Cholera 59 0.025
514
IGR001 Ige Responsiveness, Atopic 59 0.025
515
PRT058 Pure Autonomic Failure 59 0.025
516
DCT002 Ductal Carcinoma in Situ 59 0.025
517
P BRS044 Breast Adenocarcinoma 59 0.025
518
GRD007 Grade Iii Astrocytoma 59 0.025
519
P CYS018 Cystitis 59 0.025
520
BRN002 Bronchiolitis 59 0.025
521
P DNG005 Dengue Virus 59 0.025
522
FRB001 Farber Lipogranulomatosis 59 0.025
523
VLV032 Vulva Cancer 59 0.025
524
PPT005 Peptic Ulcer Disease 59 0.025
525
INC002 Inclusion Body Myositis 58 0.025
526
P SYP003 Syphilis 58 0.025
527
CRY005 Cryptococcosis 58 0.025
528
DSS008 Disease of Mental Health 58 0.025
529
CNS004 Constipation 58 0.025
530
P EPD003 Epidermolysis Bullosa Simplex 58 0.025
531
MXD005 Mixed Connective Tissue Disease 58 0.025
532
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.025
533
P OPT009 Optic Neuritis 57 0.025
534
c CHL119 Cholangitis, Primary Sclerosing 57 0.025
535
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.025
536
TNS005 Tonsillitis 57 0.025
537
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.025
538
VSC002 Vascular Dementia 57 0.025
539
P PYL005 Pyelonephritis 56 0.025
540
ALL006 Allergic Asthma 56 0.025
541
GNR004 Generalized Anxiety Disorder 56 0.025
542
ANS011 Anus Cancer 56 0.025
543
ANN002 Anencephaly 56 0.025
544
P NRF002 Neurofibromatosis 56 0.025
545
IMM140 Immunodeficiency 47 56 0.025
546
SLC006 Silicosis 56 0.025
547
ATR057 Atrioventricular Block 55 0.025
548
MCL006 Macular Retinal Edema 55 0.025
549
LMB062 Limb Ischemia 55 0.025
550
c BCT007 Bacterial Meningitis 55 0.025
551
NPH009 Nephrolithiasis 55 0.025
552
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.025
553
P PTT006 Pituitary Adenoma 55 0.025
554
P STR020 Strabismus 55 0.025
555
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
556
BRN045 Brunner Syndrome 55 0.025
557
P FNG006 Feingold Syndrome 1 55 0.025
558
END040 Endogenous Depression 55 0.025
559
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 55 0.025
560
SYN007 Synovitis 54 0.025
561
GLC003 Glucose Intolerance 54 0.025
562
P ALP008 Alopecia 54 0.025
563
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.025
564
BRN014 Bronchopneumonia 54 0.025
565
TND005 Tendinitis 54 0.025
566
THR013 Thoracic Outlet Syndrome 54 0.025
567
c AML044 Amelogenesis Imperfecta, Type Ig 54 0.025
568
DBT010 Diabetic Neuropathy 54 0.025
569
c RBN022 Robinow Syndrome, Autosomal Recessive 1 54 0.025
570
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.025
571
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 54 0.025
572
CLR030 Clear Cell Renal Cell Carcinoma 53 0.025
573
P LCH002 Lichen Planus 53 0.025
574
P EPD016 Epidermolysis Bullosa 53 0.025
575
P INS002 in Situ Carcinoma 53 0.025
576
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.025
577
c PRD040 Periodontitis, Chronic 53 0.025
578
P HML001 Hemolytic-Uremic Syndrome 53 0.025
579
IRD001 Iridocyclitis 53 0.025
580
MLN014 Melnick-Needles Syndrome 53 0.025
581
P PNC025 Panic Disorder 53 0.025
582
c FML008 Familial Retinoblastoma 53 0.025
583
ALC009 Alcoholic Liver Cirrhosis 53 0.025
584
P RTN018 Retinal Disease 53 0.025
585
EXP004 Exophthalmos 52 0.025
586
STT041 Stuttering 52 0.025
587
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.025
588
OST011 Osteomalacia 52 0.025
589
PRP016 Paraplegia 52 0.025
590
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.025
591
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.025
592
ART140 Arteries, Anomalies of 52 0.025
593
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 52 0.025
594
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.025
595
c LBR004 Leber Congenital Amaurosis 1 52 0.025
596
BWN001 Bowen-Conradi Syndrome 52 0.025
597
PTH003 Pathologic Nystagmus 52 0.025
598
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.025
599
P TRT010 Teratoma 52 0.025
600
PRV004 Periventricular Leukomalacia 52 0.025
601
LMY002 Leiomyoma 52 0.025
602
SPN051 Spondylitis 51 0.025
603
KRT009 Keratosis 51 0.025
604
MYL020 Myelomeningocele 51 0.025
605
INT079 Intrahepatic Cholangiocarcinoma 51 0.025
606
c HMC035 Hemochromatosis, Type 4 51 0.025
607
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.025
608
ASP003 Aseptic Meningitis 51 0.025
609
c SCN007 Secondary Hyperparathyroidism 51 0.025
610
END086 End Stage Renal Disease 51 0.025
611
HYP781 Hypoascorbemia 51 0.025
612
P CHL066 Cholangitis 51 0.025
613
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.025
614
c ACT078 Acute Porphyria 51 0.025
615
CHR005 Chorioamnionitis 51 0.025
616
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 51 0.025
617
PLR007 Pleural Empyema 50 0.025
618
PLR008 Pleurisy 50 0.025
619
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.025
620
ALL009 Allergic Conjunctivitis 50 0.025
621
RTN003 Retinal Ischemia 50 0.025
622
P MYS079 Miyoshi Muscular Dystrophy 50 0.025
623
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 50 0.025
624
FSC004 Fasciitis 50 0.025
625
c INF145 Infantile Liver Failure Syndrome 1 50 0.025
626
P AGG001 Aggressive Periodontitis 50 0.025
627
PLC008 Placenta Disease 50 0.025
628
NTR046 Neutrophil Migration 50 0.025
629
P OBS001 Obstructive Jaundice 50 0.025
630
MTB004 Metabolic Acidosis 50 0.025
631
DYS073 Dysphagia 50 0.025
632
VLV047 Volvulus of Midgut 49 0.025
633
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.025
634
P END046 Endometritis 49 0.025
635
CCN002 Cocaine Abuse 49 0.025
636
SLF014 Sulfite Oxidase Deficiency, Isolated 49 0.025
637
WTH001 Withdrawal Disorder 48 0.025
638
P NGH001 Night Blindness 48 0.025
639
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.025
640
P SCL009 Sclerosing Cholangitis 48 0.025
641
VTM033 Vitamin K Deficiency Bleeding 48 0.025
642
CLS016 Clostridium Difficile Colitis 48 0.025
643
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.025
644
DBT006 Diabetic Macular Edema 48 0.025
645
SPL018 Splenomegaly 48 0.025
646
DGN001 Degenerative Disc Disease 48 0.025
647
CHL147 Chlamydia Pneumonia 48 0.025
648
c VRL012 Viral Meningitis 48 0.025
649
ESN015 Eosinophilic Fasciitis 48 0.025
650
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.025
651
ART004 Aortic Atherosclerosis 47 0.025
652
SXL003 Sexual Disorder 47 0.025
653
PPL002 Papillary Carcinoma 47 0.025
654
PRC003 Proctitis 47 0.025
655
P BLR006 Biliary Tract Disease 47 0.025
656
NRN001 Neuroendocrine Carcinoma 47 0.025
657
RNL077 Renal Fibrosis 47 0.025
658
SPC010 Speech and Communication Disorders 47 0.025
659
VNZ002 Venezuelan Equine Encephalitis 47 0.025
660
ANT011 Antisocial Personality Disorder 47 0.025
661
P DNR001 Duane Retraction Syndrome 47 0.025
662
c INH020 Inherited Metabolic Disorder 47 0.025
663
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.025
664
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.025
665
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.025
666
STR103 Streptococcus Pneumonia 47 0.025
667
CRD137 Cardiogenic Shock 47 0.025
668
RYN005 Raynaud Phenomenon 47 0.025
669
LPD009 Lipid Storage Disease 46 0.025
670
ATN005 Autonomic Dysfunction 46 0.025
671
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.025
672
TTH006 Tooth Disease 46 0.025
673
MDS022 Mediastinitis 46 0.025
674
MTS001 Mutism 46 0.025
675
MYL013 Myeloperoxidase Deficiency 46 0.025
676
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.025
677
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.025
678
FCL012 Facial Paralysis 46 0.025
679
CHD004 Chudley-Mccullough Syndrome 46 0.025
680
P MTH007 Methemoglobinemia 46 0.025
681
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.025
682
GRW007 Growth Hormone Deficiency 46 0.025
683
c DRR009 Diarrhea 6 46 0.025
684
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.025
685
MXD026 Mixed Glioma 45 0.025
686
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.025
687
CNV002 Conversion Disorder 45 0.025
688
ORL013 Oral Lichen Planus 45 0.025
689
PLR022 Pleural Disease 45 0.025
690
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.025
691
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.025
692
MLK003 Melkersson-Rosenthal Syndrome 45 0.025
693
PRT019 Protein-Losing Enteropathy 45 0.025
694
BLC012 Bile Acid Malabsorption, Primary 45 0.025
695
MYF001 Myofibroma 45 0.025
696
CLD007 Cold Agglutinin Disease 45 0.025
697
GRN017 Granulocytopenia 44 0.025
698
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.025
699
CTY001 Cat Eye Syndrome 44 0.025
700
P SDR002 Siderosis 44 0.025
701
P PLM149 Palmoplantar Keratoderma and Congenital Alopecia 2 44 0.025
702
c FBR070 Febrile Seizures, Familial, 8 44 0.025
703
TNS014 Tenosynovitis 44 0.025
704
ANL017 Anal Squamous Cell Carcinoma 44 0.025
705
CHL109 Childhood Apraxia of Speech 44 0.025
706
CVD001 Covid-19 44 0.025
707
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.025
708
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.025
709
URT014 Ureterolithiasis 44 0.025
710
TND004 Tendinopathy 43 0.025
711
SMN007 Seminoma 43 0.025
712
PRS042 Prostate Disease 43 0.025
713
DRG002 Drug-Induced Hepatitis 43 0.025
714
DSC009 Discoid Lupus Erythematosus 42 0.025
715
MST004 Mast Cell Neoplasm 42 0.025
716
P AVS003 Avascular Necrosis 42 0.025
717
MRS001 Marasmus 42 0.025
718
CRV043 Cervical Dystonia 42 0.025
719
ALC010 Alcoholic Cardiomyopathy 42 0.025
720
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.025
721
SNL007 Senile Cataract 42 0.025
722
EPT021 Epithelial Recurrent Erosion Dystrophy 42 0.025
723
CRB033 Cerebral Degeneration 42 0.025
724
EXC002 Exocrine Pancreatic Insufficiency 42 0.025
725
IDP091 Idiopathic Nephrotic Syndrome 42 0.025
726
MYF002 Myofascial Pain Syndrome 42 0.025
727
MCH006 Mechanical Strabismus 42 0.025
728
CRB025 Carbohydrate Metabolic Disorder 41 0.025
729
GST020 Gastric Antral Vascular Ectasia 41 0.025
730
LMB024 Limbic Encephalitis 41 0.025
731
LTX001 Latex Allergy 41 0.025
732
WCK001 Wieacker-Wolff Syndrome 41 0.025
733
MYS001 Myositis Ossificans 41 0.025
734
PRS063 Paresthesia 41 0.025
735
VST004 Vestibular Disease 41 0.025
736
ACT088 Acute Insulin Response 41 0.025
737
KLB003 Klebsiella Pneumonia 41 0.025
738
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.025
739
FNG016 Fungal Keratitis 40 0.025
740
PLY100 Polyploidy 40 0.025
741
c SPS097 Spastic Paraplegia 13, Autosomal Dominant 39 0.025
742
LKP003 Leukoplakia 39 0.025
743
FLL031 Follicular Adenoma 39 0.025
744
CRV045 Cervical Intraepithelial Neoplasia 39 0.025
745
ESN002 Eosinophilia-Myalgia Syndrome 38 0.025
746
EXT007 Extracutaneous Mastocytoma 38 0.025
747
SMT020 Smith-Kingsmore Syndrome 38 0.025
748
LWG005 Low-Grade Astrocytoma 38 0.025
749
c PLY105 Polycystic Ovary Syndrome 1 38 0.025
750
HYP264 Hypertonia 38 0.025
751
c DNR003 Duane Retraction Syndrome 1 38 0.025
752
c MLG157 Malignant Pheochromocytoma 38 0.025
753
HYP001 Hypochromic Microcytic Anemia 38 0.025
754
OVR094 Ovarian Epithelial Cancer 38 0.025
755
c HNT011 Huntington Disease-Like 3 38 0.025
756
CNT060 Central Serous Chorioretinopathy 38 0.025
757
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.025
758
CRB009 Cerebritis 37 0.025
759
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 37 0.025
760
BLR028 Biliary Atresia, Extrahepatic 37 0.025
761
P CRB088 Cerebral Atrophy 37 0.025
762
NTL004 Nut Allergy 36 0.025
763
PLC002 Plica Syndrome 36 0.025
764
CHR028 Chronic Wasting Disease 35 0.025
765
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.025
766
PRM329 Premature Aging 35 0.025
767
END072 Endotheliitis 35 0.025
768
TLS001 Tolosa-Hunt Syndrome 35 0.025
769
WBR001 Weber Syndrome 35 0.025
770
ATX010 Ataxia Neuropathy Spectrum 34 0.025
771
CTS011 Cutis Marmorata Telangiectatica Congenita 34 0.025
772
HNS001 Hansen's Disease 34 0.025
773
NNT024 Neonatal Stroke 34 0.025
774
RHM034 Rahman Syndrome 34 0.025
776
SPT002 Septicemic Plague 33 0.025
777
c PLY136 Polydactyly, Preaxial I 33 0.025
778
ALR002 Al-Raqad Syndrome 33 0.025
779
NNS011 Nonseminomatous Germ Cell Tumor 33 0.025
780
RNL012 Renal Tuberculosis 33 0.025
781
ACT064 Acute Necrotizing Encephalitis 33 0.025
782
RCH002 Richards-Rundle Syndrome 33 0.025
783
P VSC018 Visceral Steatosis 33 0.025
784
c MJR003 Major Affective Disorder 6 33 0.025
785
c MJR006 Major Affective Disorder 5 33 0.025
786
CND006 Candida Glabrata 32 0.025
787
c BLD140 Blood Group, I System 32 0.025
788
RDT001 Radiation Cystitis 32 0.025
789
LYM043 Lymphocytic Hypophysitis 32 0.025
790
NRN002 Neuronitis 32 0.025
791
ALL007 Allergic Urticaria 31 0.025
792
INF009 Inflammatory Spondylopathy 31 0.025
793
c PRG019 Paragangliomas 2 31 0.025
794
VSC050 Vascular Malformation, Primary Intraosseous 30 0.025
795
ANS025 Anus Benign Neoplasm 30 0.025
796
ANP008 Anaplastic Oligoastrocytoma 30 0.025
797
MNG003 Mungan Syndrome 29 0.025
798
MYC088 Mycobacterium Avium Complex Infections 29 0.025
799
c EPL200 Epilepsy, Childhood Absence 1 29 0.025
800
OCC001 Occupational Dermatitis 29 0.025
801
IMM162 Immunoglobulin E Concentration, Serum 28 0.025
802
MYP120 Myopathy, Distal, with Rimmed Vacuoles 28 0.025
803
PTN004 Patent Ductus Venosus 28 0.025
804
ARG004 Argyria 27 0.025
805
c TTH010 Tooth Agenesis, Selective, 1 27 0.025
806
c ERL012 Early-Onset Glaucoma 27 0.025
807
CHL079 Children's Interstitial Lung Disease 26 0.025
808
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.025
809
ACT162 Acute Sensory Ataxic Neuropathy 26 0.025
810
MTH071 Methane Production 26 0.025
811
PRD003 Periodontosis 26 0.025
812
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.025
813
VST003 Vestibular Nystagmus 25 0.025
814
ADG002 Audiogenic Seizures 25 0.025
815
DFN341 Deafness, Unilateral 25 0.025
816
c NNN034 Noonan Syndrome 12 24 0.025
817
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.025
818
CYN003 Cyanide Poisoning 24 0.025
819
BLD163 Blood Group, Dombrock System 24 0.025
820
MLS013 Miles-Carpenter Syndrome 24 0.025
821
TXC004 Toxic Diffuse Goiter 24 0.025
822
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 23 0.025
823
SDD004 Sudden Arrhythmia Death Syndrome 22 0.025
824
MSL005 Mseleni Joint Disease 21 0.025
825
BLD165 Blood Group, Colton System 20 0.025
826
CRN311 Coronary Ostial Stenosis or Atresia 20 0.025
827
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.025
828
PYT001 Pythiosis 20 0.025
829
AND005 Androgen Insensitivity Syndrome, Mild 19 0.025
830
c AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 18 0.025
831
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.025
832
CNG491 Congenital Portosystemic Shunt 17 0.025
833
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.025
834
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 17 0.025
835
BLD137 Blood Group--Ahonen 16 0.025
836
LTH004 Lathyrism 16 0.025
837
c SPN403 Spinocerebellar Ataxia, X-Linked 2 16 0.025
838
c SPS023 Spastic Paraplegia 13 16 0.025
839
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 14 0.025
840
P CRB180 Cerebelloparenchymal Disorder Ii 13 0.025
841
DSR072 Disorder of Energy Metabolism 12 0.025
Content
Loading form....