Search results for Sulfide

572 hits were found for Sulfide

# Family MCID Name MIFTS Score
1
ISC004 Ischemia 58 0.271
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.245
3
HMC014 Homocysteinemia 53 0.196
4
P CLR023 Colorectal Cancer 99 0.192
5
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.182
6
MTH071 Methane Production 26 0.166
7
HYP266 Hypoxia 57 0.159
8
P PLM037 Pulmonary Hypertension 67 0.156
9
ANX004 Anoxia 40 0.156
10
ATH013 Atherosclerosis Susceptibility 65 0.148
11
PLM010 Pulmonary Edema 54 0.148
12
ULC004 Ulcerative Colitis 73 0.137
13
P KDN018 Kidney Disease 72 0.132
14
c ACT027 Acute Pancreatitis 60 0.132
15
P CRD119 Cardiac Arrest 67 0.129
16
HYP066 Hyperglycemia 61 0.129
17
IMP005 Impotence 52 0.129
18
P PRD008 Periodontitis 64 0.125
19
c CHR684 Chronic Kidney Disease 70 0.122
20
ACT119 Acute Promyelocytic Leukemia 63 0.122
21
CLT003 Colitis 62 0.122
22
P HRT032 Heart Disease 75 0.119
23
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.119
24
48X005 48,xyyy 39 0.119
25
P VSC007 Vascular Disease 63 0.116
26
CRB004 Cerebral Artery Occlusion 45 0.116
27
FTT001 Fatty Liver Disease 61 0.112
28
CNG034 Congestive Heart Failure 69 0.109
29
P MYC008 Myocarditis 59 0.109
30
BRN004 Brain Edema 56 0.109
31
c MCR113 Microvascular Complications of Diabetes 3 52 0.109
32
c MCR120 Microvascular Complications of Diabetes 7 47 0.109
33
c MCR130 Microvascular Complications of Diabetes 6 41 0.109
34
c MCR133 Microvascular Complications of Diabetes 4 41 0.109
35
HRW001 Hair Whorl 36 0.109
36
P NRB001 Neuroblastoma 72 0.105
37
P MYC007 Myocardial Infarction 70 0.105
38
PTY002 Pityriasis Versicolor 38 0.105
39
c ATR087 Atrial Standstill 1 75 0.101
40
P PLM036 Pulmonary Fibrosis 65 0.101
41
LVR012 Liver Cirrhosis 62 0.101
42
LNG099 Lung Disease 60 0.101
43
LMB062 Limb Ischemia 55 0.101
44
P INF037 Inflammatory Bowel Disease 54 0.101
45
DRM011 Dermatophytosis 52 0.101
46
OCL069 Ocular Motor Apraxia 51 0.101
47
P HPT023 Hepatocellular Carcinoma 100 0.097
48
P ALZ034 Alzheimer Disease 88 0.097
49
c PRC016 Pre-Eclampsia 63 0.097
50
TXC005 Toxic Shock Syndrome 62 0.097
51
P FML011 Familial Adenomatous Polyposis 72 0.093
52
ENC055 Encephalopathy, Ethylmalonic 53 0.093
53
BRN071 Brain Injury 49 0.093
54
c HYP595 Hypertension, Essential 84 0.089
55
DWN001 Down Syndrome 70 0.089
56
P LVR013 Liver Disease 68 0.089
57
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.089
58
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.089
59
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.084
60
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.084
61
DRM006 Dermatitis 61 0.084
62
P ENC018 Encephalopathy 61 0.084
63
P PNC044 Pancreatitis 61 0.084
64
PRT013 Portal Hypertension 59 0.084
65
TRM010 Traumatic Brain Injury 51 0.084
66
END086 End Stage Renal Disease 51 0.084
67
P MTH007 Methemoglobinemia 46 0.084
68
P GST053 Gastric Cancer 83 0.079
69
P PSR002 Psoriasis 62 0.079
70
P RHN004 Rhinitis 57 0.079
71
AGN016 Aging 56 0.079
72
PST011 Pustulosis of Palm and Sole 52 0.079
73
RNL077 Renal Fibrosis 47 0.079
74
ARG004 Argyria 27 0.079
75
ESP021 Esophageal Cancer 90 0.074
76
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.074
77
OST012 Osteoarthritis 78 0.074
78
IRR002 Irritable Bowel Syndrome 65 0.074
79
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.074
80
SKN016 Skin Disease 63 0.074
81
VSC002 Vascular Dementia 57 0.074
82
P LTR001 Lateral Sclerosis 54 0.074
83
URT010 Ureteral Obstruction 45 0.074
84
STR067 Stroke, Ischemic 81 0.069
85
AST005 Asthma 76 0.069
86
P RSP003 Respiratory Failure 74 0.069
87
P MLN008 Melanoma 69 0.069
88
CRB039 Cerebrovascular Disease 67 0.069
89
ALL003 Allergic Rhinitis 67 0.069
90
LSH001 Leishmaniasis 63 0.069
91
P GLM045 Glioma 63 0.069
92
LPP008 Lipoprotein Quantitative Trait Locus 62 0.069
93
P BND020 Bone Disease 59 0.069
94
VSL002 Visual Epilepsy 59 0.069
95
P BCL017 B-Cell Lymphoma 58 0.069
96
c ACT075 Acute Myocardial Infarction 57 0.069
97
P SZR006 Seizure Disorder 56 0.069
98
PPL022 Papilloma 54 0.069
99
P FBR031 Febrile Seizures 53 0.069
100
MTB004 Metabolic Acidosis 50 0.069
101
47X002 47,xyy 49 0.069
102
P RNV001 Renovascular Hypertension 48 0.069
103
GLL048 Glial Tumor 45 0.069
104
P SBR004 Seborrheic Dermatitis 45 0.069
105
P KLZ004 Kala-Azar 1 41 0.069
106
PST092 Posttransplant Acute Limbic Encephalitis 29 0.069
107
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.069
108
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.063
109
P LNG064 Lung Cancer Susceptibility 3 78 0.063
110
P PRK057 Parkinson Disease, Late-Onset 78 0.063
111
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.063
112
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.063
113
WLS001 Wilson Disease 71 0.063
114
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.063
115
P MCR115 Microvascular Complications of Diabetes 5 66 0.063
116
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.063
117
LPD008 Lipid Metabolism Disorder 62 0.063
118
ALL026 Allergic Hypersensitivity Disease 62 0.063
119
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.063
120
CHL014 Cholera 59 0.063
121
P PRP019 Peripheral Nervous System Disease 58 0.063
122
THR024 Thrombosis 57 0.063
123
P NRP001 Neuropathy 56 0.063
124
HYP005 Hypokalemia 55 0.063
125
SYN007 Synovitis 54 0.063
126
NNL006 Non-Alcoholic Steatohepatitis 54 0.063
127
c PRD040 Periodontitis, Chronic 53 0.063
128
PRP080 Peripheral Artery Disease 53 0.063
129
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.063
130
KRT009 Keratosis 51 0.063
131
ENT011 Enterocolitis 51 0.063
132
CYT002 Cytokine Deficiency 42 0.063
133
TNC002 Tinea Capitis 38 0.063
134
PLC002 Plica Syndrome 36 0.063
135
P BRS047 Breast Cancer 97 0.056
136
c LKM061 Leukemia, Acute Myeloid 84 0.056
137
CYS001 Cystic Fibrosis 81 0.056
138
c NRF023 Neurofibromatosis, Type Ii 80 0.056
139
GLB015 Glioblastoma Multiforme 75 0.056
140
P OST002 Osteoporosis 74 0.056
141
P HNT016 Huntington Disease 72 0.056
142
PRP027 Peripheral Vascular Disease 71 0.056
143
P ART022 Arthritis 69 0.056
144
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.056
145
KWS002 Kawasaki Disease 65 0.056
146
PRT036 Peritonitis 64 0.056
147
P ADN016 Adenocarcinoma 64 0.056
148
ATM095 Autoimmune Disease 62 0.056
149
P LPS004 Lupus Erythematosus 61 0.056
150
PRN019 Perinatal Necrotizing Enterocolitis 59 0.056
151
ADN018 Adenoma 59 0.056
152
ANT024 Anthrax Disease 58 0.056
153
BCT022 Bacterial Infectious Disease 56 0.056
154
VSC003 Visceral Leishmaniasis 55 0.056
155
P ART021 Arteriosclerosis 54 0.056
156
GST023 Gastric Ulcer 53 0.056
157
ART140 Arteries, Anomalies of 52 0.056
158
P LCT001 Lactic Acidosis 51 0.056
159
ACH005 Achalasia 51 0.056
160
P OVR082 Overgrowth Syndrome 50 0.056
161
NTR046 Neutrophil Migration 50 0.056
162
ENT004 Enthesopathy 49 0.056
163
HLX001 Helix Syndrome 47 0.056
164
ANP008 Anaplastic Oligoastrocytoma 30 0.056
165
CHL079 Children's Interstitial Lung Disease 26 0.056
166
CYN003 Cyanide Poisoning 24 0.056
167
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.056
168
P PRS040 Prostate Cancer 97 0.049
169
P BLD134 Bladder Cancer 79 0.049
170
c DLT002 Dilated Cardiomyopathy 79 0.049
171
CRV035 Cervical Cancer 76 0.049
172
ANX010 Anxiety 73 0.049
173
P PHC003 Pheochromocytoma 71 0.049
174
P MYP004 Myopathy 70 0.049
175
P SLP006 Sleep Apnea 69 0.049
176
SKN019 Skin Melanoma 68 0.049
177
OST159 Osteogenic Sarcoma 66 0.049
178
P SKN015 Skin Carcinoma 66 0.049
179
KRT019 Keratitis, Hereditary 65 0.049
180
CLN015 Colon Adenocarcinoma 65 0.049
181
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.049
182
c ACT068 Acute Cystitis 63 0.049
183
c OPT053 Optic Atrophy 1 63 0.049
184
P ART023 Arthropathy 62 0.049
185
NTR005 Nutritional Deficiency Disease 62 0.049
186
c SCL052 Scleroderma, Familial Progressive 61 0.049
187
CHR066 Chronic Fatigue Syndrome 61 0.049
188
SPN186 Spinal Cord Injury 60 0.049
189
THY029 Thyroid Carcinoma 59 0.049
190
P CYS018 Cystitis 59 0.049
191
GNG013 Gingivitis 59 0.049
192
P ANP001 Anaplastic Large Cell Lymphoma 58 0.049
193
CNT047 Contact Dermatitis 58 0.049
194
IRN002 Iron Metabolism Disease 57 0.049
195
P HDC001 Headache 57 0.049
196
DSS009 Disseminated Intravascular Coagulation 57 0.049
197
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.049
198
P CRD246 Cardiovascular System Disease 57 0.049
199
c ACT134 Acute Liver Failure 56 0.049
200
P GST044 Gastritis 56 0.049
201
HMS001 Hemosiderosis 54 0.049
202
PRS045 Prostatic Hypertrophy 53 0.049
203
OCL006 Ocular Hypertension 53 0.049
204
PRS021 Prostatic Adenoma 51 0.049
205
RTN003 Retinal Ischemia 50 0.049
206
HYP006 Hypertensive Heart Disease 49 0.049
207
PRS129 Prostatic Hyperplasia, Benign 49 0.049
208
URM002 Uremia 49 0.049
209
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.049
210
CLN019 Colonic Disease 47 0.049
211
RTN020 Retinal Vascular Disease 46 0.049
212
P BRB001 Beriberi 46 0.049
213
ADR040 Adrenal Gland Pheochromocytoma 46 0.049
214
SQM002 Squamous Cell Papilloma 46 0.049
215
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.049
216
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.049
217
OBS082 Obstructive Nephropathy 42 0.049
218
P RRH023 Rare Hereditary Hemochromatosis 41 0.049
219
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.049
220
CND006 Candida Glabrata 32 0.049
221
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.049
222
P OVR042 Ovarian Cancer 88 0.040
223
MYL069 Myeloma, Multiple 85 0.040
224
MLR004 Malaria 81 0.040
225
P SCH015 Schizophrenia 74 0.040
226
P RTN024 Retinoblastoma 73 0.040
227
c LKM063 Leukemia, Chronic Myeloid 72 0.040
228
ADN011 Adenoid Cystic Carcinoma 70 0.040
229
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.040
230
P LKM062 Leukemia, Acute Lymphoblastic 69 0.040
231
P PNM007 Pneumonia 68 0.040
232
c BSL007 Basal Cell Carcinoma 68 0.040
233
P LKM002 Leukemia 68 0.040
234
P HPT021 Hepatitis 67 0.040
235
P TRN020 Turner Syndrome 67 0.040
236
P HYP098 Hypereosinophilic Syndrome 67 0.040
237
P MLG056 Malignant Hyperthermia 67 0.040
238
c MGR028 Migraine with or Without Aura 1 67 0.040
239
ANG054 Angina Pectoris 66 0.040
240
P DMN002 Dementia 66 0.040
241
P MSC005 Muscular Dystrophy 66 0.040
242
c MCR129 Microvascular Complications of Diabetes 1 66 0.040
243
P ADL010 Adult Respiratory Distress Syndrome 65 0.040
244
GT001 Gout 64 0.040
245
P RHB003 Rhabdomyosarcoma 63 0.040
246
P HML002 Hemolytic Anemia 63 0.040
247
P CRN300 Coronary Heart Disease 1 63 0.040
248
c FNC043 Fanconi Anemia, Complementation Group E 62 0.040
249
c HPT003 Hepatitis a 62 0.040
250
P ESP024 Esophagitis 62 0.040
251
BLL006 Bullous Pemphigoid 62 0.040
252
ALC006 Alcoholic Hepatitis 61 0.040
253
P MYL006 Myeloid Leukemia 60 0.040
254
SQM006 Squamous Cell Carcinoma 60 0.040
255
ORL011 Oral Cancer 60 0.040
256
c ACT071 Acute Kidney Failure 60 0.040
257
BRN002 Bronchiolitis 59 0.040
258
GST045 Gastroenteritis 59 0.040
259
PPT005 Peptic Ulcer Disease 59 0.040
260
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.040
261
EYD002 Eye Disease 58 0.040
262
CNS004 Constipation 58 0.040
263
P CND004 Candidiasis 58 0.040
264
GLS018 Glass Syndrome 57 0.040
265
BRN056 Bronchopulmonary Dysplasia 57 0.040
266
P EXN002 Exanthem 57 0.040
267
SCH014 Schistosomiasis 57 0.040
268
PRS047 Prostatitis 56 0.040
269
GST050 Gastrointestinal System Disease 56 0.040
270
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.040
271
URN010 Urinary Tract Obstruction 55 0.040
272
P SLM003 Salmonellosis 55 0.040
273
HYP060 Hyperinsulinism 54 0.040
274
GLC003 Glucose Intolerance 54 0.040
275
DBT010 Diabetic Neuropathy 54 0.040
276
P EPD016 Epidermolysis Bullosa 53 0.040
277
OST016 Osteochondrosis 53 0.040
278
KRT006 Keratoconjunctivitis 53 0.040
279
P HMC002 Homocystinuria 53 0.040
280
P HMR003 Hemorrhagic Disease 53 0.040
281
P ACT008 Actinic Keratosis 53 0.040
282
DNT012 Dental Caries 53 0.040
283
c FML008 Familial Retinoblastoma 53 0.040
284
P RTN018 Retinal Disease 53 0.040
285
CLR109 Colorectal Adenocarcinoma 51 0.040
286
BLP005 Blepharitis 50 0.040
287
CRT013 Carotid Stenosis 50 0.040
288
EPD006 Epidermolysis Bullosa Acquisita 49 0.040
289
BNR002 Bone Resorption Disease 48 0.040
290
SPL018 Splenomegaly 48 0.040
291
DGN001 Degenerative Disc Disease 48 0.040
292
P MRC003 Mercury Poisoning 48 0.040
293
SXL003 Sexual Disorder 47 0.040
294
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.040
295
CRD137 Cardiogenic Shock 47 0.040
296
SYN036 Syncope 45 0.040
297
RTR008 Root Resorption 45 0.040
298
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.040
299
CYN002 Cyanosis, Transient Neonatal 45 0.040
300
HPT004 Hepatic Coma 45 0.040
301
ACT003 Acute Kidney Tubular Necrosis 45 0.040
302
GNG011 Gingival Disease 45 0.040
303
CYS019 Cystathioninuria 45 0.040
304
PTT037 Pituitary Tumors 44 0.040
305
c PCH010 Pachyonychia Congenita 3 44 0.040
306
CRN045 Corneal Dystrophy and Perceptive Deafness 44 0.040
307
ORL015 Oral Squamous Cell Carcinoma 43 0.040
308
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.040
309
P RRT020 Rare Tumor 41 0.040
310
c MCR112 Microvascular Complications of Diabetes 2 41 0.040
311
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.040
312
SKN020 Skin Papilloma 39 0.040
313
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.040
314
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.040
315
NRD001 Neurodermatitis 35 0.040
316
PYR009 Pyridoxine Deficiency Anemia 34 0.040
318
CNT018 Central Nervous System Leukemia 34 0.040
319
PLY150 Polykaryocytosis Inducer 31 0.040
320
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 0.040
321
CYT018 Cytochrome P450 2d6 Variant 27 0.040
322
FTL064 Fetal Methylmercury Syndrome 26 0.040
323
PRQ002 Paraquat Poisoning 26 0.040
324
HVY002 Heavy Metal Poisoning 22 0.040
325
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 17 0.040
326
P LNG032 Lung Cancer 98 0.028
327
c SYS001 Systemic Lupus Erythematosus 86 0.028
329
P PNC035 Pancreatic Cancer 84 0.028
330
P ATX030 Ataxia-Telangiectasia 82 0.028
331
P RHM011 Rheumatoid Arthritis 80 0.028
332
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.028
333
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.028
334
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.028
335
PHN003 Phenylketonuria 75 0.028
336
BRN028 Brain Cancer 74 0.028
337
CRH001 Crohn's Disease 74 0.028
338
c HYP836 Hypercholesterolemia, Familial, 1 73 0.028
339
c THR092 Thrombophilia Due to Thrombin Defect 73 0.028
340
MSC157 Muscular Dystrophy, Duchenne Type 72 0.028
341
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.028
342
P MLT020 Multiple Sclerosis 72 0.028
343
P AMY004 Amyloidosis 70 0.028
344
LGH007 Leigh Syndrome 70 0.028
345
P FRG001 Fragile X Syndrome 70 0.028
346
WRN001 Werner Syndrome 69 0.028
347
LYM133 Lymphoma, Hodgkin, Classic 69 0.028
348
P LPR021 Leprosy 3 69 0.028
349
BRN024 Bronchitis 68 0.028
350
RCK004 Rickets 68 0.028
351
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.028
352
GST092 Gastroesophageal Reflux 67 0.028
353
c INF071 Inflammatory Bowel Disease 1 67 0.028
354
c HMP029 Hemophilia a 67 0.028
355
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.028
356
MYC006 Mycosis Fungoides 66 0.028
357
c FML021 Familial Hypercholesterolemia 66 0.028
358
c FML346 Familial Adenomatous Polyposis 1 66 0.028
359
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.028
360
HYP056 Hypoglycemia 66 0.028
361
CHG001 Chagas Disease 66 0.028
362
P HYD006 Hydrocephalus 66 0.028
363
P MNN013 Meningitis 66 0.028
364
P DRM053 Dermatitis, Atopic 66 0.028
365
MYL031 Myeloproliferative Neoplasm 66 0.028
366
c SML038 Small Cell Cancer of the Lung 65 0.028
367
P HRS035 Hirschsprung Disease 1 65 0.028
368
P CNJ013 Conjunctivitis 65 0.028
369
P MTR014 Motor Neuron Disease 65 0.028
370
BRR014 Barrett Esophagus 65 0.028
371
P THY023 Thymoma 65 0.028
372
P DBT009 Diabetes Mellitus 64 0.028
373
c JVN010 Juvenile Rheumatoid Arthritis 64 0.028
374
CLR108 Colorectal Adenoma 64 0.028
375
DSM004 Desmoid Tumor 64 0.028
376
OST017 Osteomyelitis 64 0.028
377
P NTR004 Neutropenia 63 0.028
378
PLG002 Plague 63 0.028
379
c MLG084 Malignant Fibrous Histiocytoma 63 0.028
380
P LMY004 Leiomyosarcoma 63 0.028
381
c GLC092 Glaucoma, Primary Open Angle 62 0.028
382
c SVR001 Severe Acute Respiratory Syndrome 62 0.028
383
P HYP750 Hypertriglyceridemia, Familial 62 0.028
384
P VSC011 Vasculitis 62 0.028
385
CTN007 Cutaneous Leishmaniasis 62 0.028
386
CHL068 Cholestasis 61 0.028
387
PSR001 Psoriatic Arthritis 61 0.028
388
OST003 Osteonecrosis 61 0.028
389
c PNS012 Paine Syndrome 61 0.028
390
RTN017 Retinal Detachment 61 0.028
391
DCB001 Decubitus Ulcer 61 0.028
392
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.028
393
HPT019 Hepatic Encephalopathy 60 0.028
394
CRD223 Cardiac Arrhythmia 60 0.028
395
P CTR002 Cataract 60 0.028
396
STT001 Status Epilepticus 60 0.028
397
P EPS003 Episodic Ataxia 59 0.028
398
P SLP005 Sleep Disorder 59 0.028
399
HLC007 Helicobacter Pylori Infection 59 0.028
400
P INT070 Intestinal Obstruction 58 0.028
401
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.028
402
NWB001 Newborn Respiratory Distress Syndrome 58 0.028
403
P BNC003 Bone Cancer 58 0.028
404
c DWL002 Dowling-Degos Disease 1 58 0.028
405
LYM027 Lymphopenia 58 0.028
406
P GLM007 Glomerulonephritis 57 0.028
407
MCR013 Microphthalmia 57 0.028
408
CHL067 Cholecystitis 57 0.028
409
P FTL001 Fetal Alcohol Syndrome 57 0.028
410
P PLY018 Polycythemia 56 0.028
411
P FBR017 Fibrosarcoma 56 0.028
412
TRN018 Transitional Cell Carcinoma 56 0.028
413
ALL006 Allergic Asthma 56 0.028
414
P MTC069 Mitochondrial Disorders 56 0.028
415
ALL010 Allergic Contact Dermatitis 56 0.028
416
FLR001 Filarial Elephantiasis 55 0.028
417
ATR057 Atrioventricular Block 55 0.028
418
P DRR001 Diarrhea 55 0.028
419
ACT058 Active Peptic Ulcer Disease 55 0.028
420
P HYP076 Hyperthyroidism 55 0.028
421
FLR002 Filariasis 55 0.028
422
P DBT005 Diabetes Insipidus 55 0.028
423
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.028
424
AMN003 Amnestic Disorder 54 0.028
425
AMN001 Amenorrhea 54 0.028
426
SLP001 Sleeping Sickness 54 0.028
427
CLR030 Clear Cell Renal Cell Carcinoma 53 0.028
428
TRC023 Trichinosis 53 0.028
429
P RTN016 Retinal Degeneration 53 0.028
430
MST005 Mastitis 53 0.028
431
TXC002 Toxic Encephalopathy 53 0.028
432
P INT068 Intestinal Disease 53 0.028
433
c CNT035 Central Nervous System Disease 52 0.028
434
PRP016 Paraplegia 52 0.028
435
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.028
436
P RCT021 Rectum Cancer 52 0.028
437
DYS015 Dysentery 52 0.028
438
c THY107 Thymoma, Familial 52 0.028
439
LGN006 Legionnaire Disease 52 0.028
440
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.028
441
TLN003 Telangiectasis 52 0.028
442
c VRL005 Viral Pneumonia 52 0.028
443
STV003 Stuve-Wiedemann Syndrome 52 0.028
444
PNG002 Pain Agnosia 51 0.028
445
P HMP007 Hemophilia 51 0.028
446
CLC001 Calciphylaxis 51 0.028
447
P PRC012 Pericardial Effusion 51 0.028
448
TNG007 Tongue Carcinoma 51 0.028
449
P AST007 Astrocytoma 51 0.028
450
BHR001 Behr Syndrome 51 0.028
451
CRV040 Cervix Carcinoma 51 0.028
452
P ECL001 Eclampsia 50 0.028
453
c SVR005 Severe Pre-Eclampsia 50 0.028
454
AZS001 Azoospermia 50 0.028
455
c HRD202 Hereditary Lymphedema I 50 0.028
456
MCP006 Mucoepidermoid Carcinoma 50 0.028
457
P AGG001 Aggressive Periodontitis 50 0.028
458
PLC008 Placenta Disease 50 0.028
459
NPH010 Nephrosclerosis 50 0.028
460
OPT003 Opiate Dependence 50 0.028
461
c INF023 Inflammatory Breast Carcinoma 50 0.028
462
PLP001 Pulpitis 49 0.028
463
P OPN001 Open-Angle Glaucoma 49 0.028
464
SCT005 Scott Syndrome 49 0.028
465
ACR002 Acrocapitofemoral Dysplasia 48 0.028
466
WTH001 Withdrawal Disorder 48 0.028
467
ADT003 Auditory System Disease 48 0.028
468
ASP007 Aspiration Pneumonia 48 0.028
469
c LYM144 Lymphatic Malformation 1 48 0.028
470
BLD044 Bladder Disease 48 0.028
471
HMP001 Hemopericardium 48 0.028
472
VTM002 Vitamin B12 Deficiency 48 0.028
473
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.028
474
MCC002 Mucocutaneous Leishmaniasis 47 0.028
475
THY128 Thyroid Tumor 47 0.028
476
P RNL015 Renal Hypertension 47 0.028
477
P ENC008 Encephalocele 47 0.028
478
c INH020 Inherited Metabolic Disorder 47 0.028
479
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.028
480
STM006 Stomach Disease 47 0.028
481
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.028
482
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.028
483
P CRC039 Coarctation of Aorta 47 0.028
484
TST044 Testicular Torsion 47 0.028
485
STR103 Streptococcus Pneumonia 47 0.028
486
CHR074 Choriocarcinoma 47 0.028
487
CMP002 Campylobacteriosis 46 0.028
488
LYM019 Lymphosarcoma 46 0.028
489
ATN005 Autonomic Dysfunction 46 0.028
490
BCK003 Background Diabetic Retinopathy 46 0.028
491
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.028
492
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.028
493
CMP034 Complete Androgen Insensitivity Syndrome 46 0.028
494
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.028
495
FLL008 Folliculitis 46 0.028
496
HDN002 Head Injury 46 0.028
497
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.028
498
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.028
499
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.028
500
NWC001 Newcastle Disease 45 0.028
501
c CRN278 Craniosynostosis 1 45 0.028
502
URL001 Urolithiasis 45 0.028
503
SPS057 Spasticity 45 0.028
504
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.028
505
LRY022 Laryngoonychocutaneous Syndrome 44 0.028
506
DBT008 Diabetic Angiopathy 44 0.028
507
DWR001 Dwarfism 44 0.028
508
PTY001 Pityriasis Rosea 44 0.028
509
P FBR003 Fibrous Histiocytoma 44 0.028
510
CRB027 Cerebellar Disease 44 0.028
511
ART006 Arthus Reaction 44 0.028
512
DMP001 Dumping Syndrome 44 0.028
513
CVD001 Covid-19 44 0.028
514
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.028
515
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.028
516
CRB090 Cerebral Hypoxia 44 0.028
517
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.028
518
TST015 Testicular Disease 43 0.028
519
MCR011 Microinvasive Gastric Cancer 43 0.028
520
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.028
521
P HYP265 Hypotonia 43 0.028
522
ALC010 Alcoholic Cardiomyopathy 42 0.028
523
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.028
524
ATX019 Ataxia with Vitamin E Deficiency 42 0.028
525
P NSL008 Nasal Cavity Cancer 41 0.028
526
MSN004 Mesenchymal Cell Neoplasm 41 0.028
527
DYS011 Dyskinesia of Esophagus 41 0.028
528
PRS063 Paresthesia 41 0.028
529
ALC005 Alcoholic Pancreatitis 40 0.028
530
PLY100 Polyploidy 40 0.028
531
ART008 Arteriosclerosis Obliterans 40 0.028
532
WLL004 Wallerian Degeneration 39 0.028
533
PCH007 Pouchitis 39 0.028
534
P PRP021 Peripheral Nervous System Neoplasm 39 0.028
535
CVT001 Cavitary Optic Disc Anomalies 38 0.028
536
CDQ001 Cauda Equina Syndrome 38 0.028
537
SCL001 Scalp Dermatosis 38 0.028
538
P CRB088 Cerebral Atrophy 37 0.028
539
c HRD007 Hereditary Lymphedema 37 0.028
540
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 37 0.028
541
HRN029 Hearing Loss, Noise-Induced 37 0.028
542
SYS071 Systemic Autoimmune Disease 37 0.028
543
HYP114 Hypertensive Nephropathy 36 0.028
544
BRK012 Broken Heart Syndrome 35 0.028
545
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.028
546
CHR178 Chromosomal Triplication 35 0.028
547
PRM329 Premature Aging 35 0.028
548
c PST106 Post-Cardiac Arrest Syndrome 35 0.028
549
HNS001 Hansen's Disease 34 0.028
550
c LKM005 Leukemia, T-Cell, Chronic 34 0.028
551
PPL052 Papillomatosis, Confluent and Reticulated 33 0.028
552
HND015 Hand Skill, Relative 33 0.028
553
CYT014 Cytochrome P450 Oxidoreductase Deficiency 32 0.028
554
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.028
555
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.028
556
c CNG439 Congenital Lymphedema 32 0.028
557
PLR005 Pleuropneumonia 31 0.028
558
c SBR001 Seborrheic Infantile Dermatitis 30 0.028
559
VRT001 Vertebral Artery Occlusion 30 0.028
560
GRV012 Grover's Disease 30 0.028
562
MXL017 Maxillary Cancer 29 0.028
563
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.028
564
HYP160 Hyperkeratosis Lenticularis Perstans 27 0.028
565
c TRC073 Treacher Collins Syndrome 2 27 0.028
566
ACT162 Acute Sensory Ataxic Neuropathy 26 0.028
567
c CRN256 Craniosynostosis 6 23 0.028
568
P SLF001 Sulfhemoglobinemia 23 0.028
569
c MGL029 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3 23 0.028
570
ACQ008 Acquired Hyperkeratosis 22 0.028
571
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.028
572
LTH043 Lithium Transport 18 0.028
Content
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