Search results for Methionine

939 hits were found for Methionine

# Family MCID Name MIFTS Score
1
MTH074 Methionine Adenosyltransferase I/iii Deficiency 42 6.344
2
HYP003 Hypermethioninemia 40 6.097
3
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 36 4.279
4
MTH011 Methionine Adenosyltransferase Deficiency 18 3.071
5
MTH075 Methionine Malabsorption Syndrome 15 2.983
6
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 32 2.200
7
GLY015 Glycine N-Methyltransferase Deficiency 39 2.168
8
MTH046 Methylmalonic Acidemia Without Homocystinuria 26 2.146
9
ALP077 Alpha-Methylacetoacetic Aciduria 55 2.119
10
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 38 2.119
11
DSR079 Disorder of Methionine Cycle and Sulfur Amino Acid Metabolism 4 2.098
12
MTH021 Methylmalonic Acidemia with Homocystinuria 46 2.069
13
HMC014 Homocysteinemia 53 0.343
14
P LVR013 Liver Disease 68 0.262
15
FTT001 Fatty Liver Disease 61 0.262
16
NNL006 Non-Alcoholic Steatohepatitis 54 0.257
17
P HMC002 Homocystinuria 53 0.248
18
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.225
19
GLL048 Glial Tumor 45 0.194
20
P GLM045 Glioma 63 0.193
21
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.188
22
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.187
23
P HPT023 Hepatocellular Carcinoma 100 0.183
24
P VSC007 Vascular Disease 63 0.182
25
NRL016 Neural Tube Defects 82 0.180
26
LVR012 Liver Cirrhosis 62 0.175
27
CHL068 Cholestasis 61 0.165
28
GLB015 Glioblastoma Multiforme 75 0.154
29
P CLR023 Colorectal Cancer 99 0.152
30
DPR016 Depression 63 0.143
31
CHL045 Choline Deficiency Disease 39 0.140
32
ADN018 Adenoma 59 0.138
33
P NRB001 Neuroblastoma 72 0.136
34
MNT002 Mental Depression 58 0.136
35
HLX001 Helix Syndrome 47 0.132
36
VSL002 Visual Epilepsy 59 0.125
37
P SZR006 Seizure Disorder 56 0.125
38
VTM002 Vitamin B12 Deficiency 48 0.125
39
P MJR001 Major Depressive Disorder 68 0.123
40
P ALZ034 Alzheimer Disease 88 0.113
41
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.113
42
MGL001 Megaloblastic Anemia 51 0.113
43
P AST007 Astrocytoma 51 0.113
44
P HPT021 Hepatitis 67 0.110
45
P BRS047 Breast Cancer 97 0.108
46
INS024 Insulin-Like Growth Factor I 79 0.108
47
P ENC018 Encephalopathy 61 0.108
48
DSR002 Disorders of Intracellular Cobalamin Metabolism 31 0.105
49
ATH013 Atherosclerosis Susceptibility 65 0.102
50
P HYP069 Hyperparathyroidism 63 0.102
51
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.099
52
DWN001 Down Syndrome 70 0.096
53
c INH020 Inherited Metabolic Disorder 47 0.096
54
c MNN043 Meningioma, Familial 74 0.093
55
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.093
56
P PHC003 Pheochromocytoma 71 0.093
57
LPP008 Lipoprotein Quantitative Trait Locus 62 0.093
58
MNN042 Meningioma, Radiation-Induced 62 0.093
59
SPN021 Spinal Meningioma 50 0.093
60
ADR040 Adrenal Gland Pheochromocytoma 46 0.093
61
SCR001 Secretory Meningioma 41 0.093
62
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.093
63
MYL069 Myeloma, Multiple 85 0.090
64
c MLG068 Malignant Glioma 46 0.090
65
c PCH010 Pachyonychia Congenita 3 44 0.090
66
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.090
67
P PRS040 Prostate Cancer 97 0.087
68
P SCH015 Schizophrenia 74 0.087
69
P AMY004 Amyloidosis 70 0.087
70
c PRM005 Primary Hyperparathyroidism 58 0.087
71
ART140 Arteries, Anomalies of 52 0.087
72
48X005 48,xyyy 39 0.087
73
PPL052 Papillomatosis, Confluent and Reticulated 33 0.087
74
P PNC035 Pancreatic Cancer 84 0.083
75
P GST053 Gastric Cancer 83 0.083
76
P CRN300 Coronary Heart Disease 1 63 0.083
77
P PRN023 Prion Disease 57 0.083
78
P MTH008 Methylmalonic Acidemia 50 0.083
79
HPT004 Hepatic Coma 45 0.083
80
P MDL005 Medulloblastoma 77 0.080
81
c HYP836 Hypercholesterolemia, Familial, 1 73 0.080
82
DFC004 Deficiency Anemia 70 0.080
83
P OLG002 Oligodendroglioma 67 0.080
84
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.080
85
P HML002 Hemolytic Anemia 63 0.080
86
c PRC016 Pre-Eclampsia 63 0.080
87
HPT019 Hepatic Encephalopathy 60 0.080
88
P CTR002 Cataract 60 0.080
89
GRD007 Grade Iii Astrocytoma 59 0.080
90
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.080
91
AGN016 Aging 56 0.080
92
PYR009 Pyridoxine Deficiency Anemia 34 0.080
93
CYS001 Cystic Fibrosis 81 0.076
94
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.076
95
BRN028 Brain Cancer 74 0.076
96
P LKM062 Leukemia, Acute Lymphoblastic 69 0.076
97
P LYM118 Lymphoma 68 0.076
98
SRC014 Sarcoma 65 0.076
99
P ADN016 Adenocarcinoma 64 0.076
100
c HPT001 Hepatitis C 62 0.076
101
NTR005 Nutritional Deficiency Disease 62 0.076
102
P BCL017 B-Cell Lymphoma 58 0.076
103
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.076
104
P CRD246 Cardiovascular System Disease 57 0.076
105
END040 Endogenous Depression 55 0.076
106
SPN035 Spindle Cell Sarcoma 53 0.076
107
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.076
108
HRN029 Hearing Loss, Noise-Induced 37 0.076
109
PRC051 Paracetamol Poisoning 30 0.076
110
P OVR042 Ovarian Cancer 88 0.072
111
c THR092 Thrombophilia Due to Thrombin Defect 73 0.072
112
c HPT073 Hepatitis C Virus 72 0.072
113
CRT072 Creutzfeldt-Jakob Disease 70 0.072
114
ALC007 Alcohol Dependence 66 0.072
115
LPD008 Lipid Metabolism Disorder 62 0.072
116
P PRM006 Primary Biliary Cirrhosis 62 0.072
117
VSC002 Vascular Dementia 57 0.072
118
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.072
119
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.072
120
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.072
121
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.072
122
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.072
123
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.072
124
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.072
125
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.072
126
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.072
127
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.072
128
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.072
129
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.068
130
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.068
131
P HRT032 Heart Disease 75 0.068
132
P ATS364 Autism 70 0.068
133
P DMN002 Dementia 66 0.068
134
c ACT068 Acute Cystitis 63 0.068
135
ATM095 Autoimmune Disease 62 0.068
136
CRC021 Carcinosarcoma 62 0.068
137
ACQ007 Acquired Immunodeficiency Syndrome 60 0.068
138
ISC004 Ischemia 58 0.068
139
P HDC001 Headache 57 0.068
140
HYP266 Hypoxia 57 0.068
141
NRT001 Neurotic Disorder 53 0.068
142
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.068
143
PRT029 Parathyroid Adenoma 50 0.068
144
MTB004 Metabolic Acidosis 50 0.068
145
NWC001 Newcastle Disease 45 0.068
146
CHL065 Cholangiocarcinoma 68 0.064
147
P LKM002 Leukemia 68 0.064
148
HYP056 Hypoglycemia 66 0.064
149
CLR108 Colorectal Adenoma 64 0.064
150
P RHB003 Rhabdomyosarcoma 63 0.064
151
LSH001 Leishmaniasis 63 0.064
152
CYS013 Cystinuria 63 0.064
153
HYP066 Hyperglycemia 61 0.064
154
P PNC044 Pancreatitis 61 0.064
155
LNG099 Lung Disease 60 0.064
156
P ALC033 Alcohol Use Disorder 58 0.064
157
P MYS005 Myositis 56 0.064
158
P LTR001 Lateral Sclerosis 54 0.064
159
P RCT021 Rectum Cancer 52 0.064
160
INT079 Intrahepatic Cholangiocarcinoma 51 0.064
161
P HYP265 Hypotonia 43 0.064
162
CYT002 Cytokine Deficiency 42 0.064
163
P KLZ004 Kala-Azar 1 41 0.064
164
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 13 0.064
165
P LNG032 Lung Cancer 98 0.059
166
c HYP595 Hypertension, Essential 84 0.059
167
STR067 Stroke, Ischemic 81 0.059
168
P BLD134 Bladder Cancer 79 0.059
169
OST012 Osteoarthritis 78 0.059
170
P PRK057 Parkinson Disease, Late-Onset 78 0.059
171
P KDN018 Kidney Disease 72 0.059
172
P EPL164 Epilepsy 71 0.059
173
P MYP004 Myopathy 70 0.059
174
P MLN008 Melanoma 69 0.059
175
c MGR028 Migraine with or Without Aura 1 67 0.059
176
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.059
177
P MSC005 Muscular Dystrophy 66 0.059
178
CRN036 Craniopharyngioma 65 0.059
179
P PLM036 Pulmonary Fibrosis 65 0.059
180
c HPT003 Hepatitis a 62 0.059
181
c BRN108 Branchiootic Syndrome 1 62 0.059
182
ALC006 Alcoholic Hepatitis 61 0.059
183
P BNG030 Benign Ependymoma 60 0.059
184
c HPT016 Hepatitis B 59 0.059
185
THR024 Thrombosis 57 0.059
186
P BPL003 Bipolar Disorder 56 0.059
187
BRN004 Brain Edema 56 0.059
188
P MLN007 Male Infertility 55 0.059
189
HYP060 Hyperinsulinism 54 0.059
190
CLL010 Cellular Ependymoma 54 0.059
191
P ART021 Arteriosclerosis 54 0.059
192
P CNT005 Central Nervous System Lymphoma 53 0.059
193
PNG002 Pain Agnosia 51 0.059
194
OCL069 Ocular Motor Apraxia 51 0.059
195
CCC002 Coccidiosis 51 0.059
196
END086 End Stage Renal Disease 51 0.059
197
P TMP001 Temporal Lobe Epilepsy 50 0.059
198
P OBS001 Obstructive Jaundice 50 0.059
199
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.059
200
c PRM226 Primary Central Nervous System Lymphoma 48 0.059
201
P BNG032 Benign Mesothelioma 46 0.059
202
URL001 Urolithiasis 45 0.059
203
c MJR024 Major Affective Disorder 9 41 0.059
204
ALL014 Allergic Encephalomyelitis 38 0.059
205
c MJR022 Major Affective Disorder 8 38 0.059
206
HRW001 Hair Whorl 36 0.059
207
PYR016 Pyridoxine Deficiency 30 0.059
208
P GLM040 Glioma Susceptibility 1 81 0.054
209
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.054
210
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.054
211
P RTN024 Retinoblastoma 73 0.054
212
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.054
213
HMN044 Human Immunodeficiency Virus Type 1 71 0.054
214
P SRC025 Sarcoidosis 1 70 0.054
215
P MYC007 Myocardial Infarction 70 0.054
216
EWN003 Ewing Sarcoma 69 0.054
217
CRB039 Cerebrovascular Disease 67 0.054
218
OST159 Osteogenic Sarcoma 66 0.054
219
CLF027 Cleft Palate, Isolated 64 0.054
220
ANR007 Anorexia Nervosa 63 0.054
221
DRM006 Dermatitis 61 0.054
222
GST033 Gestational Diabetes 61 0.054
223
P INF032 Infertility 57 0.054
224
IRN002 Iron Metabolism Disease 57 0.054
225
SFT003 Soft Tissue Sarcoma 56 0.054
226
MCS002 Mucositis 56 0.054
227
P PLY019 Polyneuropathy 56 0.054
228
P DRR001 Diarrhea 55 0.054
229
P PTT006 Pituitary Adenoma 55 0.054
230
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 54 0.054
231
P TRM003 Tremor 54 0.054
232
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 0.054
233
PRN011 Pernicious Anemia 53 0.054
234
c FML008 Familial Retinoblastoma 53 0.054
235
STM007 Stomatitis 50 0.054
236
47X002 47,xyy 49 0.054
237
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.054
238
CYS019 Cystathioninuria 45 0.054
239
HMP009 Haemophilus Influenzae 43 0.054
240
ANX004 Anoxia 40 0.054
241
SCR011 Scrapie 39 0.054
242
c LKM005 Leukemia, T-Cell, Chronic 34 0.054
243
MLR004 Malaria 81 0.048
244
CRV035 Cervical Cancer 76 0.048
245
ULC004 Ulcerative Colitis 73 0.048
246
P MLT020 Multiple Sclerosis 72 0.048
247
P HNT016 Huntington Disease 72 0.048
248
WLS001 Wilson Disease 71 0.048
249
LYM133 Lymphoma, Hodgkin, Classic 69 0.048
250
BRN024 Bronchitis 68 0.048
251
P TRN020 Turner Syndrome 67 0.048
252
c RHB024 Rhabdomyosarcoma 2 67 0.048
253
PRT037 Pertussis 65 0.048
254
P HRP006 Herpes Simplex 65 0.048
255
TBC004 Tobacco Addiction 64 0.048
256
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.048
257
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.048
258
TRN015 Transient Cerebral Ischemia 63 0.048
259
c SVR001 Severe Acute Respiratory Syndrome 62 0.048
260
P TRC086 Trichohepatoenteric Syndrome 1 62 0.048
261
P PRP029 Porphyria 62 0.048
262
THY029 Thyroid Carcinoma 59 0.048
263
CYS010 Cystinosis 59 0.048
264
P TYR004 Tyrosinemia 58 0.048
265
FBR047 Fibromyalgia 58 0.048
266
P GLM007 Glomerulonephritis 57 0.048
267
c ACT134 Acute Liver Failure 56 0.048
268
DFF005 Diffuse Large B-Cell Lymphoma 55 0.048
269
HMS001 Hemosiderosis 54 0.048
270
PPL022 Papilloma 54 0.048
271
MST005 Mastitis 53 0.048
272
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.048
273
PTH003 Pathologic Nystagmus 52 0.048
274
c INF145 Infantile Liver Failure Syndrome 1 50 0.048
275
VCC001 Vaccinia 49 0.048
276
ATS010 Autosomal Recessive Disease 48 0.048
277
MCR020 Microsporidiosis 48 0.048
278
LYM019 Lymphosarcoma 46 0.048
279
MXD026 Mixed Glioma 45 0.048
280
CYS009 Cystadenoma 44 0.048
281
KWS001 Kwashiorkor 44 0.048
282
c MLG079 Malignant Pleural Mesothelioma 42 0.048
283
49X006 49, Xxxxy Syndrome 41 0.048
284
P MLG074 Malignant Mesenchymoma 40 0.048
285
AMN002 Amino Acid Metabolic Disorder 39 0.048
286
P VSC018 Visceral Steatosis 33 0.048
287
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.048
288
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 29 0.048
289
ARG004 Argyria 27 0.048
290
ESP021 Esophageal Cancer 90 0.042
291
c SYS001 Systemic Lupus Erythematosus 86 0.042
293
CNN003 Conn's Syndrome 79 0.042
294
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.042
295
KPS004 Kaposi Sarcoma 75 0.042
296
PHN003 Phenylketonuria 75 0.042
297
ADR007 Adrenoleukodystrophy 75 0.042
298
P RSP003 Respiratory Failure 74 0.042
299
LPT014 Leptin Deficiency or Dysfunction 74 0.042
300
P OST002 Osteoporosis 74 0.042
301
P CNR004 Cone-Rod Dystrophy 2 73 0.042
302
ANX010 Anxiety 73 0.042
303
ACR007 Acromegaly 71 0.042
304
PRP027 Peripheral Vascular Disease 71 0.042
305
c CHR684 Chronic Kidney Disease 70 0.042
306
ADL002 Adult Syndrome 70 0.042
307
P HYP086 Hypothyroidism 69 0.042
308
ART016 Aortic Aneurysm 69 0.042
309
P INF038 Influenza 68 0.042
310
PNC129 Pancreatic Adenocarcinoma 68 0.042
311
P PLM037 Pulmonary Hypertension 67 0.042
312
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.042
313
TTN003 Tetanus 65 0.042
314
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.042
315
PRP001 Propionic Acidemia 65 0.042
316
BRR014 Barrett Esophagus 65 0.042
317
P DBT009 Diabetes Mellitus 64 0.042
318
P ANR048 Aniridia 1 63 0.042
319
SKN016 Skin Disease 63 0.042
320
CLT003 Colitis 62 0.042
321
P HYP750 Hypertriglyceridemia, Familial 62 0.042
322
c PNS012 Paine Syndrome 61 0.042
323
DPH001 Diphtheria 60 0.042
324
c ACT027 Acute Pancreatitis 60 0.042
325
ACN002 Acanthosis Nigricans 60 0.042
326
SQM006 Squamous Cell Carcinoma 60 0.042
327
STT001 Status Epilepticus 60 0.042
328
P THL005 Thalassemia 60 0.042
329
P MCR010 Microcephaly 59 0.042
330
CHL014 Cholera 59 0.042
331
P CYS018 Cystitis 59 0.042
332
ANR040 Aneurysm 59 0.042
333
PPT005 Peptic Ulcer Disease 59 0.042
334
INC002 Inclusion Body Myositis 58 0.042
335
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.042
336
P PLV020 Pelvic Organ Prolapse 57 0.042
337
P FBR017 Fibrosarcoma 56 0.042
338
P NRP001 Neuropathy 56 0.042
339
BCT022 Bacterial Infectious Disease 56 0.042
340
SPN041 Spinal Cord Disease 56 0.042
341
HYP005 Hypokalemia 55 0.042
342
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.042
343
VSC003 Visceral Leishmaniasis 55 0.042
344
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.042
345
FCL014 Focal Epilepsy 54 0.042
346
P INF037 Inflammatory Bowel Disease 54 0.042
347
PLM012 Pulmonary Sarcoidosis 53 0.042
348
P PLM006 Pulmonary Alveolar Proteinosis 53 0.042
349
GST023 Gastric Ulcer 53 0.042
350
c GLL024 Gallbladder Disease 1 53 0.042
351
c VRL010 Viral Hepatitis 52 0.042
352
GLM004 Gliomatosis Cerebri 52 0.042
353
PLS009 Plasma Cell Neoplasm 51 0.042
354
P THR015 Thrombophilia 51 0.042
355
P CHL066 Cholangitis 51 0.042
356
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.042
357
P OVR082 Overgrowth Syndrome 50 0.042
358
P ECL001 Eclampsia 50 0.042
359
PLC008 Placenta Disease 50 0.042
360
FTL002 Fatal Familial Insomnia 49 0.042
361
ENT004 Enthesopathy 49 0.042
362
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.042
363
ANT018 Anthracosis 48 0.042
364
CNT033 Central Nervous System Cancer 47 0.042
365
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.042
366
GRW007 Growth Hormone Deficiency 46 0.042
367
SQM002 Squamous Cell Papilloma 46 0.042
368
KR002 Kuru 45 0.042
369
PTT037 Pituitary Tumors 44 0.042
370
MCR017 Macrocytic Anemia 44 0.042
371
MRG013 Mirage Syndrome 43 0.042
372
c SRC023 Sarcoidosis 2 43 0.042
373
P MJR007 Major Affective Disorder 1 43 0.042
374
P CLS010 Cluster Headache 42 0.042
375
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.042
376
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.042
377
GRM004 Germinoma 40 0.042
378
CRV045 Cervical Intraepithelial Neoplasia 39 0.042
379
LWG005 Low-Grade Astrocytoma 38 0.042
380
ADR022 Adrenomyeloneuropathy 38 0.042
381
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 38 0.042
382
DYS006 Dysembryoplastic Neuroepithelial Tumor 38 0.042
383
CRY036 Cryptogenic Cirrhosis 36 0.042
384
OLG006 Oligoastrocytoma 35 0.042
385
ATX010 Ataxia Neuropathy Spectrum 34 0.042
386
BRN034 Brain Meningioma 33 0.042
387
ACT064 Acute Necrotizing Encephalitis 33 0.042
388
c PRS136 Prostate Cancer, Hereditary, 6 33 0.042
389
c PRS130 Prostate Cancer, Hereditary, 8 32 0.042
390
PLY150 Polykaryocytosis Inducer 31 0.042
391
ISL099 Isolated Methylmalonic Acidemia 29 0.042
392
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 28 0.042
393
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.042
394
PRS131 Prostate Cancer/brain Cancer Susceptibility 25 0.042
395
AMN012 Aminoacidopathies 21 0.042
396
BLD137 Blood Group--Ahonen 16 0.042
397
IMM167 Immune Deficiency Disease 78 0.034
398
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.034
399
P LNG064 Lung Cancer Susceptibility 3 78 0.034
400
SVR004 Severe Combined Immunodeficiency 73 0.034
401
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.034
402
CNG034 Congestive Heart Failure 69 0.034
403
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.034
404
P ART022 Arthritis 69 0.034
405
SKN019 Skin Melanoma 68 0.034
406
P THR014 Thrombocytopenia 67 0.034
407
P CRD119 Cardiac Arrest 67 0.034
408
FCT007 Factor Vii Deficiency 67 0.034
409
BRK010 Burkitt Lymphoma 67 0.034
410
P FLL037 Follicular Lymphoma 67 0.034
411
THY111 Thyroid Carcinoma, Familial Medullary 67 0.034
412
P CHR012 Chronic Granulomatous Disease 67 0.034
413
PSY004 Psychotic Disorder 67 0.034
414
P PRP003 Porphyria Cutanea Tarda 67 0.034
415
c ATS007 Autism Spectrum Disorder 67 0.034
416
c TYR012 Tyrosinemia, Type I 66 0.034
417
ANG054 Angina Pectoris 66 0.034
418
c FML021 Familial Hypercholesterolemia 66 0.034
419
P ATR011 Atrial Fibrillation 66 0.034
420
P DRM053 Dermatitis, Atopic 66 0.034
421
c MCL013 Mucolipidosis Iv 66 0.034
422
c FML001 Familial Atrial Fibrillation 65 0.034
423
P VNW001 Von Willebrand's Disease 65 0.034
424
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.034
425
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.034
426
c DBT099 Diabetes Mellitus, Type I 65 0.034
427
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.034
428
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.034
429
P PRD008 Periodontitis 64 0.034
430
PLM031 Poliomyelitis 64 0.034
431
HYP020 Hyperprolactinemia 64 0.034
432
OST017 Osteomyelitis 64 0.034
433
PLG002 Plague 63 0.034
434
c MLG084 Malignant Fibrous Histiocytoma 63 0.034
435
P PSR002 Psoriasis 62 0.034
436
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.034
437
P ART023 Arthropathy 62 0.034
438
P VSC011 Vasculitis 62 0.034
439
ALL026 Allergic Hypersensitivity Disease 62 0.034
440
GLY010 Glycine Encephalopathy 62 0.034
441
c SCL052 Scleroderma, Familial Progressive 61 0.034
442
P ENC004 Encephalitis 61 0.034
443
CHR066 Chronic Fatigue Syndrome 61 0.034
444
c WLM018 Wilms Tumor 5 61 0.034
445
VRL011 Viral Infectious Disease 61 0.034
446
P KDN017 Kidney Cancer 60 0.034
447
P SNS001 Sensorineural Hearing Loss 60 0.034
448
c ACT071 Acute Kidney Failure 60 0.034
449
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.034
450
PRT013 Portal Hypertension 59 0.034
451
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.034
452
CHL123 Chlamydia 59 0.034
453
P PRD006 Prader-Willi Syndrome 59 0.034
454
P BRS044 Breast Adenocarcinoma 59 0.034
455
P DNG005 Dengue Virus 59 0.034
456
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.034
457
P SYP003 Syphilis 58 0.034
458
CNS004 Constipation 58 0.034
459
GLS018 Glass Syndrome 57 0.034
460
c ACT075 Acute Myocardial Infarction 57 0.034
461
c MST023 Mesothelioma, Malignant 57 0.034
462
SCH014 Schistosomiasis 57 0.034
463
P PLY011 Polycystic Ovary Syndrome 56 0.034
464
TRN018 Transitional Cell Carcinoma 56 0.034
465
PLS011 Plasmacytoma 56 0.034
466
ANN002 Anencephaly 56 0.034
467
HMG005 Hemoglobinopathy 56 0.034
468
SLC006 Silicosis 56 0.034
469
P HYP076 Hyperthyroidism 55 0.034
470
P DBT005 Diabetes Insipidus 55 0.034
471
PRP030 Purpura 54 0.034
472
HMN009 Hemangioblastoma 54 0.034
473
AMN003 Amnestic Disorder 54 0.034
474
GLC003 Glucose Intolerance 54 0.034
475
GNG004 Ganglioglioma 54 0.034
476
P ALP008 Alopecia 54 0.034
477
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.034
478
THR013 Thoracic Outlet Syndrome 54 0.034
479
SLP001 Sleeping Sickness 54 0.034
480
c HNT010 Huntington Disease-Like 1 53 0.034
481
CRH005 Crohn's Colitis 53 0.034
482
P RTN016 Retinal Degeneration 53 0.034
483
FNG017 Fungal Infectious Disease 53 0.034
484
CLF001 Cleft Lip 53 0.034
485
P RTN022 Retinal Vein Occlusion 53 0.034
486
ALC009 Alcoholic Liver Cirrhosis 53 0.034
487
P SML001 Small Cell Carcinoma 52 0.034
488
PST011 Pustulosis of Palm and Sole 52 0.034
489
P MSC003 Muscular Atrophy 52 0.034
490
MTH078 Methylmalonic Aciduria, Cblb Type 51 0.034
491
CLR109 Colorectal Adenocarcinoma 51 0.034
492
TRM010 Traumatic Brain Injury 51 0.034
493
FBR008 Fibrillary Astrocytoma 51 0.034
494
c SCN007 Secondary Hyperparathyroidism 51 0.034
495
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.034
496
HYP781 Hypoascorbemia 51 0.034
497
c HNT004 Huntington Disease-Like 2 50 0.034
498
FLT009 Folate Malabsorption, Hereditary 50 0.034
499
THY125 Thyroid Gland Medullary Carcinoma 50 0.034
500
TRY001 Trypanosomiasis 50 0.034
501
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.034
502
P END046 Endometritis 49 0.034
503
CHL004 Cholelithiasis 49 0.034
504
c BPL002 Bipolar I Disorder 49 0.034
505
URM002 Uremia 49 0.034
506
BCT004 Bacteriuria 49 0.034
507
BNR002 Bone Resorption Disease 48 0.034
508
BBS001 Babesiosis 48 0.034
509
PLC007 Placental Abruption 48 0.034
510
CLF056 Cleft Lip with or Without Cleft Palate 47 0.034
511
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.034
512
LPD004 Lipoid Nephrosis 46 0.034
513
CNT019 Central Neurocytoma 46 0.034
514
P BRB001 Beriberi 46 0.034
515
P MTH007 Methemoglobinemia 46 0.034
516
EPD015 Epidemic Typhus 45 0.034
517
CRB004 Cerebral Artery Occlusion 45 0.034
518
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 45 0.034
519
P CHR345 Chronic Pain 44 0.034
520
PPL001 Papillary Adenoma 44 0.034
521
ANP009 Anaplastic Oligodendroglioma 43 0.034
522
FNC007 Functioning Pituitary Adenoma 43 0.034
523
MDD018 Middle East Respiratory Syndrome 43 0.034
524
ATX019 Ataxia with Vitamin E Deficiency 42 0.034
525
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.034
526
MYF002 Myofascial Pain Syndrome 42 0.034
527
PLM020 Pleomorphic Xanthoastrocytoma 41 0.034
528
HPR006 Heparin Cofactor Ii Deficiency 40 0.034
529
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.034
530
CRB086 Cerebral Aneurysms 40 0.034
531
SCR015 Scarlet Fever 39 0.034
532
PTT003 Pituitary-Dependent Cushing's Disease 39 0.034
533
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.034
534
c CHR682 Chronic Bilirubin Encephalopathy 39 0.034
535
ANT019 Anterograde Amnesia 38 0.034
536
AMN006 Aminoaciduria 38 0.034
537
ATM052 Autoimmune Disease 1 37 0.034
538
P CRB088 Cerebral Atrophy 37 0.034
539
c PLZ002 Pelizaeus-Merzbacher-Like Disease 36 0.034
540
c MJR008 Major Affective Disorder 2 35 0.034
542
c MJR023 Major Affective Disorder 7 33 0.034
543
MCR025 Microhydranencephaly 33 0.034
544
c MJR003 Major Affective Disorder 6 33 0.034
545
c MJR006 Major Affective Disorder 5 33 0.034
546
HLT002 Halothane Hepatitis 32 0.034
547
WLD005 Wild Type Attr Amyloidosis 32 0.034
548
HGH041 High-Grade Astrocytoma 32 0.034
549
FNT004 Fainting 30 0.034
550
ANP008 Anaplastic Oligoastrocytoma 30 0.034
551
ACT228 Acute Radiation Syndrome 29 0.034
552
c DFN116 Deafness, Autosomal Recessive 74 29 0.034
553
MYC088 Mycobacterium Avium Complex Infections 29 0.034
554
c MJR004 Major Affective Disorder 4 28 0.034
555
MST020 Mast Cell Activation Syndrome 26 0.034
556
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.034
557
HRP008 Herpes Simiae 25 0.034
558
ADG002 Audiogenic Seizures 25 0.034
559
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.034
560
AND005 Androgen Insensitivity Syndrome, Mild 19 0.034
561
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.034
562
c LKM061 Leukemia, Acute Myeloid 84 0.024
563
P RHM011 Rheumatoid Arthritis 80 0.024
564
c NRF023 Neurofibromatosis, Type Ii 80 0.024
565
c DLT002 Dilated Cardiomyopathy 79 0.024
566
P RTN008 Retinitis Pigmentosa 79 0.024
567
P LYN001 Lynch Syndrome 77 0.024
568
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.024
569
END057 Endometrial Cancer 74 0.024
570
SCK003 Sickle Cell Anemia 74 0.024
571
c BTT014 Beta-Thalassemia 74 0.024
572
CRH001 Crohn's Disease 74 0.024
573
MSC157 Muscular Dystrophy, Duchenne Type 72 0.024
574
P FML011 Familial Adenomatous Polyposis 72 0.024
575
OTT002 Otitis Media 72 0.024
576
GST040 Gastric Adenocarcinoma 70 0.024
577
MYL009 Myelodysplastic Syndrome 70 0.024
578
LGH007 Leigh Syndrome 70 0.024
579
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.024
580
ADN011 Adenoid Cystic Carcinoma 70 0.024
581
P TTR001 Tetralogy of Fallot 70 0.024
582
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.024
583
c PNC108 Pancreatitis, Hereditary 70 0.024
584
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.024
585
P MPL001 Maple Syrup Urine Disease 69 0.024
586
P ANG001 Angelman Syndrome 69 0.024
587
P SYS005 Systemic Scleroderma 68 0.024
588
P MYC084 Mycobacterium Tuberculosis 1 68 0.024
589
P MYS003 Myasthenia Gravis 68 0.024
590
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.024
591
CNN005 Connective Tissue Disease 68 0.024
592
RCK004 Rickets 68 0.024
593
GST092 Gastroesophageal Reflux 67 0.024
594
OMN001 Omenn Syndrome 67 0.024
595
CRP001 Carpal Tunnel Syndrome 67 0.024
596
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 66 0.024
597
P NSP012 Nasopharyngeal Carcinoma 66 0.024
598
P MCR115 Microvascular Complications of Diabetes 5 66 0.024
600
AND002 Androgen Insensitivity Syndrome 66 0.024
601
P MNN013 Meningitis 66 0.024
602
KHL003 Kohlschutter-Tonz Syndrome 65 0.024
603
P AGM001 Agammaglobulinemia 65 0.024
604
P DYS154 Dystonia 65 0.024
605
KRT019 Keratitis, Hereditary 65 0.024
606
P MTR014 Motor Neuron Disease 65 0.024
607
IRR002 Irritable Bowel Syndrome 65 0.024
608
CHY002 Chylomicron Retention Disease 65 0.024
609
c WLM013 Wilms Tumor 1 65 0.024
610
P ADL010 Adult Respiratory Distress Syndrome 65 0.024
611
P THY023 Thymoma 65 0.024
612
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.024
613
P CHR071 Charcot-Marie-Tooth Disease 65 0.024
614
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.024
615
P GLC113 Galactosemia I 64 0.024
616
DGR001 Digeorge Syndrome 64 0.024
617
P NTR004 Neutropenia 63 0.024
618
TYP007 Typhoid Fever 63 0.024
619
ACT119 Acute Promyelocytic Leukemia 63 0.024
620
c OPT053 Optic Atrophy 1 63 0.024
621
c ALP101 Alpha-Thalassemia 62 0.024
622
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.024
623
c FNC043 Fanconi Anemia, Complementation Group E 62 0.024
624
P PLY014 Polycystic Kidney Disease 62 0.024
625
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.024
626
P BCK002 Beckwith-Wiedemann Syndrome 62 0.024
627
LSC001 Lesch-Nyhan Syndrome 62 0.024
628
c ANM038 Anemia, Autoimmune Hemolytic 62 0.024
629
HSH003 Hashimoto Thyroiditis 62 0.024
630
CTN007 Cutaneous Leishmaniasis 62 0.024
631
MDD011 Mood Disorder 62 0.024
632
TXC005 Toxic Shock Syndrome 62 0.024
633
MSL001 Measles 62 0.024
634
P INT143 Interstitial Cystitis 61 0.024
635
P SJG008 Sjogren Syndrome 61 0.024
636
ARG002 Argininosuccinic Aciduria 61 0.024
637
P LPS004 Lupus Erythematosus 61 0.024
638
SPN186 Spinal Cord Injury 60 0.024
639
HRP004 Herpes Zoster 60 0.024
640
P TST021 Testicular Germ Cell Tumor 60 0.024
641
P VNT002 Ventricular Septal Defect 60 0.024
642
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.024
643
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.024
644
VRC005 Varicose Veins 60 0.024
645
CHC001 Chickenpox 60 0.024
646
INS001 Insulinoma 60 0.024
647
ETN001 Eating Disorder 60 0.024
648
ANT009 Antithrombin Iii Deficiency 59 0.024
649
SPP011 Suppression of Tumorigenicity 12 59 0.024
650
P MYC008 Myocarditis 59 0.024
651
P AXN002 Axenfeld-Rieger Syndrome 59 0.024
652
P LKD001 Leukodystrophy 59 0.024
653
P BRN022 Bronchiectasis 59 0.024
654
P SLP005 Sleep Disorder 59 0.024
655
PLM033 Pulmonary Embolism 59 0.024
656
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.024
657
AVN001 Avian Influenza 59 0.024
658
GST045 Gastroenteritis 59 0.024
659
GLB001 Gilbert Syndrome 58 0.024
660
ANT024 Anthrax Disease 58 0.024
661
PST028 Post-Traumatic Stress Disorder 58 0.024
662
P INT070 Intestinal Obstruction 58 0.024
663
RBS001 Rabies 58 0.024
664
CMP010 Complex Regional Pain Syndrome 58 0.024
665
P MMP001 Mumps 58 0.024
666
CHL028 Childhood Type Dermatomyositis 58 0.024
667
LYM027 Lymphopenia 58 0.024
668
P CND004 Candidiasis 58 0.024
669
P PRP019 Peripheral Nervous System Disease 58 0.024
670
LNG108 Langerhans Cell Histiocytosis 58 0.024
671
P GLL018 Gallbladder Cancer 57 0.024
672
c CHL119 Cholangitis, Primary Sclerosing 57 0.024
673
ARG007 Argininemia 57 0.024
674
P FTL001 Fetal Alcohol Syndrome 57 0.024
675
BLR008 Bilirubin Metabolic Disorder 57 0.024
676
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.024
677
CYT008 Cytomegalovirus Infection 57 0.024
678
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.024
679
PPL058 Papilloma of Choroid Plexus 56 0.024
680
P PLY018 Polycythemia 56 0.024
681
P ADL017 Adult T-Cell Leukemia 56 0.024
682
P MLT074 Multiple Endocrine Neoplasia 56 0.024
683
ERY051 Erythroleukemia, Familial 56 0.024
684
P MTC069 Mitochondrial Disorders 56 0.024
685
P TMR010 Tumor Predisposition Syndrome 56 0.024
686
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.024
687
P NRF002 Neurofibromatosis 56 0.024
688
GRS011 Gerstmann-Straussler Disease 56 0.024
689
P PNM006 Pneumoconiosis 56 0.024
690
P RST002 Restrictive Cardiomyopathy 56 0.024
691
AND020 Androgen Insensitivity, Partial 56 0.024
692
P GST044 Gastritis 56 0.024
693
HPT022 Hepatoblastoma 56 0.024
694
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.024
695
P AGN002 Agnosia 55 0.024
696
ICH001 Ichthyosis Vulgaris 55 0.024
697
AMB001 Amebiasis 55 0.024
698
c BCT007 Bacterial Meningitis 55 0.024
699
P PLM034 Pulmonary Emphysema 55 0.024
700
P GRV001 Graves' Disease 55 0.024
701
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.024
702
GNG005 Gangliocytoma 55 0.024
703
PRN001 Purine Nucleoside Phosphorylase Deficiency 55 0.024
704
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.024
705
P LRY044 Larynx Cancer 55 0.024
706
SYN007 Synovitis 54 0.024
707
TRD006 Tardive Dyskinesia 54 0.024
708
GLS001 Gliosarcoma 54 0.024
709
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.024
710
LYM040 Lymphoblastic Lymphoma 54 0.024
711
WST005 West Nile Virus 54 0.024
712
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.024
713
CLL003 Cellulitis 54 0.024
714
P TCD001 Tic Disorder 53 0.024
715
c CNT016 Central Retinal Vein Occlusion 53 0.024
716
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.024
717
ENC055 Encephalopathy, Ethylmalonic 53 0.024
718
P HML001 Hemolytic-Uremic Syndrome 53 0.024
719
P SHR001 Short Bowel Syndrome 53 0.024
720
GTR002 Goiter 53 0.024
721
GSG001 Gas Gangrene 53 0.024
722
P INT068 Intestinal Disease 53 0.024
723
TRC008 Trachoma 53 0.024
724
OVR059 Ovary Adenocarcinoma 53 0.024
725
c MCR113 Microvascular Complications of Diabetes 3 52 0.024
726
DMY004 Demyelinating Disease 52 0.024
727
PLM014 Pleomorphic Adenoma 52 0.024
728
CRB151 Cerebral Creatine Deficiency Syndrome 1 52 0.024
729
DYS015 Dysentery 52 0.024
730
THY030 Thyroid Gland Disease 52 0.024
731
P CNG436 Congenital Disorder of Deglycosylation 52 0.024
732
c THY107 Thymoma, Familial 52 0.024
733
P THY032 Thyroiditis 52 0.024
734
FML037 Female Breast Cancer 52 0.024
735
P TRT010 Teratoma 52 0.024
736
RYS001 Reye Syndrome 51 0.024
737
c PNC106 Pancreatic Agenesis 1 51 0.024
738
P LCT001 Lactic Acidosis 51 0.024
739
MYL020 Myelomeningocele 51 0.024
740
NRM004 Neuroma 51 0.024
741
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.024
742
TLR001 Tularemia 51 0.024
743
P HYP040 Hypospadias 51 0.024
744
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 0.024
745
HYP081 Hypolipoproteinemia 51 0.024
746
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.024
747
P MMB011 Membranous Nephropathy 50 0.024
748
P HYP077 Hypertrichosis 50 0.024
749
PLR008 Pleurisy 50 0.024
750
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 0.024
751
RTN003 Retinal Ischemia 50 0.024
752
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.024
753
HPT014 Hepatorenal Syndrome 50 0.024
754
AZS001 Azoospermia 50 0.024
755
CRT013 Carotid Stenosis 50 0.024
756
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 50 0.024
757
NTR046 Neutrophil Migration 50 0.024
758
c LRG001 Large Cell Carcinoma 50 0.024
759
c VNW010 Von Willebrand Disease, Type 2 50 0.024
760
NPH010 Nephrosclerosis 50 0.024
761
HYP017 Hypophosphatemia 50 0.024
762
RBF001 Riboflavin Deficiency 49 0.024
763
LFT001 Left Bundle Branch Hemiblock 49 0.024
764
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.024
765
SPT005 Spotted Fever 49 0.024
766
P CRV031 Cervical Adenocarcinoma 49 0.024
767
DYS009 Dysthymic Disorder 49 0.024
768
BRN071 Brain Injury 49 0.024
769
MTC005 Mitochondrial Metabolism Disease 49 0.024
770
P CNG003 Congenital Dyserythropoietic Anemia 49 0.024
771
P MGR001 Migraine Without Aura 49 0.024
772
HST010 Histiocytosis 48 0.024
773
HYP043 Hyperandrogenism 48 0.024
774
OLF005 Olfactory Neuroblastoma 48 0.024
775
P SCL009 Sclerosing Cholangitis 48 0.024
776
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.024
777
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.024
778
P RNV001 Renovascular Hypertension 48 0.024
779
PNC034 Pancreas Disease 48 0.024
780
SPL018 Splenomegaly 48 0.024
781
CHL147 Chlamydia Pneumonia 48 0.024
782
FBR009 Fibrous Dysplasia 48 0.024
783
P TRT019 Torticollis 48 0.024
784
MLT006 Multidrug-Resistant Tuberculosis 48 0.024
785
ART004 Aortic Atherosclerosis 47 0.024
786
SXL003 Sexual Disorder 47 0.024
787
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 47 0.024
788
PRC003 Proctitis 47 0.024
789
NDL007 Nodular Goiter 47 0.024
790
RNL077 Renal Fibrosis 47 0.024
791
ACT084 Acute Stress Disorder 47 0.024
792
c MCR120 Microvascular Complications of Diabetes 7 47 0.024
793
KRT002 Keratomalacia 47 0.024
794
HYP082 Hypopharynx Cancer 47 0.024
795
RTN023 Retinitis 46 0.024
796
ATN005 Autonomic Dysfunction 46 0.024
797
TTH006 Tooth Disease 46 0.024
798
MYL013 Myeloperoxidase Deficiency 46 0.024
799
c ALP104 Alport Syndrome 3, Autosomal Dominant 46 0.024
800
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.024
801
P PLL002 Pellagra 46 0.024
802
TRP008 Tropical Calcific Pancreatitis 46 0.024
803
MYX001 Myxopapillary Ependymoma 46 0.024
804
VGN019 Vaginal Discharge 46 0.024
805
CWP001 Cowpox 46 0.024
806
c DRR009 Diarrhea 6 46 0.024
807
TRN022 Transcobalamin Ii Deficiency 45 0.024
808
c HRD039 Hereditary Amyloidosis 45 0.024
809
URT010 Ureteral Obstruction 45 0.024
810
HMR023 Hemorrhagic Cystitis 45 0.024
811
LYD001 Leydig Cell Tumor 45 0.024
812
STS002 Situs Inversus 45 0.024
813
SWN001 Swine Influenza 45 0.024
814
BRN032 Brain Glioma 45 0.024
815
CRT015 Carotid Artery Occlusion 45 0.024
816
MLN073 Melanosis, Neurocutaneous 45 0.024
817
SPS057 Spasticity 45 0.024
818
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.024
819
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 44 0.024
820
DWR001 Dwarfism 44 0.024
821
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.024
822
P FBR003 Fibrous Histiocytoma 44 0.024
823
c RNG023 Ring Chromosome 7 44 0.024
824
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.024
825
CLN003 Clonorchiasis 44 0.024
826
c PRM038 Primary Agammaglobulinemia 44 0.024
827
CVD001 Covid-19 44 0.024
828
ADN022 Adenylosuccinase Deficiency 44 0.024
829
BNM001 Bone Marrow Cancer 43 0.024
830
GLL017 Gallbladder Adenocarcinoma 43 0.024
831
ENC005 Encephalomalacia 43 0.024
832
SDD008 Sudden Sensorineural Hearing Loss 43 0.024
833
LWC001 Low Compliance Bladder 43 0.024
834
RTC009 Reticulum Cell Sarcoma 43 0.024
835
PNM013 Pneumococcal Meningitis 42 0.024
836
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 42 0.024
838
MRS001 Marasmus 42 0.024
839
SNL007 Senile Cataract 42 0.024
840
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.024
841
NRR001 Neuroretinitis 42 0.024
842
ANC002 Anca-Associated Vasculitis 41 0.024
843
c MCR130 Microvascular Complications of Diabetes 6 41 0.024
844
c MCR133 Microvascular Complications of Diabetes 4 41 0.024
845
TTT001 Tatton-Brown-Rahman Syndrome 41 0.024
846
P RRH023 Rare Hereditary Hemochromatosis 41 0.024
847
MRP001 Morphine Dependence 41 0.024
848
RDN001 Reading Disorder 40 0.024
849
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.024
850
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.024
851
JWD001 Jawad Syndrome 40 0.024
852
CHN004 Chondroblastoma 40 0.024
853
PYR004 Pyuria 40 0.024
854
ALC005 Alcoholic Pancreatitis 40 0.024
855
P PRG092 Pregnancy Loss, Recurrent 1 40 0.024
856
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.024
857
PLY100 Polyploidy 40 0.024
858
SPN221 Spina Bifida Occulta 39 0.024
859
HNZ004 Heinz Body Anemias 39 0.024
860
c ATR062 Atrial Septal Defect 1 39 0.024
861
c PRG020 Paragangliomas 3 39 0.024
862
HYP141 Hyperphenylalaninemia 39 0.024
863
CRB001 Cerebral Lymphoma 39 0.024
864
c RTN066 Retinitis Pigmentosa 4 39 0.024
865
P PRC031 Preeclampsia/eclampsia 1 38 0.024
866
HYP264 Hypertonia 38 0.024
867
PRP005 Parapsoriasis 38 0.024
868
OVR094 Ovarian Epithelial Cancer 38 0.024
869
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 38 0.024
870
c HNT011 Huntington Disease-Like 3 38 0.024
871
c SYS043 Systemic Lupus Erythematosus 1 38 0.024
872
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.024
873
CTN011 Cutaneous Porphyria 38 0.024
874
P FML187 Familial Hypertension 37 0.024
875
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.024
876
NRS005 Neurosarcoidosis 36 0.024
877
THR123 Thrombotic Microangiopathy 36 0.024
878
BRN018 Borna Disease 36 0.024
879
AMN007 Aminoacylase 1 Deficiency 36 0.024
880
PRS011 Persian Gulf Syndrome 36 0.024
881
PLC002 Plica Syndrome 36 0.024
883
c ATM045 Autoimmune Glomerulonephritis 36 0.024
884
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.024
885
CHR028 Chronic Wasting Disease 35 0.024
886
c MCR312 Microphthalmia, Syndromic 10 35 0.024
887
CHR178 Chromosomal Triplication 35 0.024
888
PRM329 Premature Aging 35 0.024
889
ACT149 Acetaminophen Metabolism 35 0.024
890
c NNS007 Nonsyndromic Deafness 35 0.024
891
KSH001 Keshan Disease 34 0.024
892
MYT011 Myotonia 34 0.024
893
MTH047 Methanol Poisoning 34 0.024
894
NND010 Nondisjunction 34 0.024
895
SPR006 Sparganosis 34 0.024
896
VSL003 Visual Agnosia 34 0.024
897
EXT054 Extra-Adrenal Pheochromocytoma 34 0.024
898
ALR002 Al-Raqad Syndrome 33 0.024
899
HND015 Hand Skill, Relative 33 0.024
900
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 32 0.024
901
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 0.024
902
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 32 0.024
903
P SPN042 Spinal Cord Ependymoma 31 0.024
904
P ALB003 Albinism-Deafness Syndrome 31 0.024
905
c FML324 Familial Porphyria Cutanea Tarda 31 0.024
906
NNS045 Non-Specific Syndromic Intellectual Disability 31 0.024
907
EXN003 Exencephaly 31 0.024
908
PLR005 Pleuropneumonia 31 0.024
909
GST029 Gastric Cardia Adenocarcinoma 31 0.024
910
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 0.024
911
BRN049 Brain Tumor, Childhood 29 0.024
912
DSR074 Disorder of Purine Metabolism 29 0.024
913
PST092 Posttransplant Acute Limbic Encephalitis 29 0.024
914
RHM013 Rheumatoid Nodulosis 28 0.024
915
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.024
916
c ATS006 Autosomal Recessive Nonsyndromic Deafness 27 0.024
917
CYT018 Cytochrome P450 2d6 Variant 27 0.024
918
CLR011 Clear Cell Ependymoma 27 0.024
919
c RNG015 Ring Chromosome 2 26 0.024
920
ACT094 Acute Articular Rheumatism 26 0.024
921
THY006 Thymus Lymphoma 26 0.024
922
MTH040 Methylmalonyl-Coa Epimerase Deficiency 26 0.024
923
SHR097 Short Tarsus with Absence of Lower Eyelashes 26 0.024
924
NRM022 Neurometabolic Disease 25 0.024
925
BLD163 Blood Group, Dombrock System 24 0.024
926
c ERY064 Erythrocytosis, Familial, 6 23 0.024
927
LRY027 Laryngeal Papillomatosis 23 0.024
928
CHR158 Charles Bonnet Syndrome 23 0.024
929
c MTC129 Mitochondrial Dna Depletion Syndrome 15 22 0.024
930
DRG025 Drug-Induced Hearing Loss 22 0.024
931
LYM053 Lymphomatous Thyroiditis 22 0.024
932
P SPN237 Spina Bifida Aperta 20 0.024
933
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.024
934
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.024
935
LTH004 Lathyrism 16 0.024
936
P PLT029 Platelet Groups--Ko System 16 0.024
937
c ART151 Aortic Aneurysm, Familial Abdominal, 2 14 0.024
938
MTH081 Mthfr Gene Variant 14 0.024
939
SLN002 Selenium Poisoning 11 0.024
Content
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