Search results for pyrophosphate

472 hits were found for pyrophosphate

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 41 9.112
2
FML307 Familial Calcium Pyrophosphate Deposition 40 7.871
3
P CHN059 Chondrocalcinosis 52 4.547
4
P ART023 Arthropathy 62 0.402
5
GT001 Gout 64 0.284
6
c ACT075 Acute Myocardial Infarction 57 0.263
7
IRN002 Iron Metabolism Disease 57 0.220
8
OST012 Osteoarthritis 78 0.215
9
P AMY004 Amyloidosis 70 0.206
10
P HYP069 Hyperparathyroidism 63 0.196
11
c CHR684 Chronic Kidney Disease 70 0.182
12
P KDN018 Kidney Disease 72 0.179
13
SYN007 Synovitis 54 0.177
14
BNR002 Bone Resorption Disease 48 0.177
15
PLC002 Plica Syndrome 36 0.177
16
P HYP035 Hypophosphatasia 61 0.165
17
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.155
18
ANK001 Ankylosis 51 0.152
19
INT007 Intermediate Coronary Syndrome 55 0.149
20
END086 End Stage Renal Disease 51 0.149
21
DFC004 Deficiency Anemia 70 0.142
22
P ART022 Arthritis 69 0.142
23
c HMC039 Hemochromatosis, Type 1 74 0.138
24
CRY024 Crystal Arthropathies 20 0.135
25
ANG054 Angina Pectoris 66 0.127
26
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.119
27
P BRB001 Beriberi 46 0.114
28
P HYP086 Hypothyroidism 69 0.110
29
URL001 Urolithiasis 45 0.110
30
SPT004 Septic Arthritis 58 0.105
31
P PSD087 Pseudoxanthoma Elasticum 65 0.100
32
IRN001 Iron Deficiency Anemia 59 0.100
33
c KNN009 Kenny-Caffey Syndrome, Type 1 34 0.100
34
CNG034 Congestive Heart Failure 69 0.095
35
CHG001 Chagas Disease 66 0.095
36
P BND020 Bone Disease 59 0.095
37
P CHN012 Chondrosarcoma 56 0.095
38
FRZ001 Frozen Shoulder 53 0.095
39
BRS064 Bursitis 48 0.095
40
CLC006 Calcinosis 48 0.095
41
c PRM005 Primary Hyperparathyroidism 58 0.090
42
HYP005 Hypokalemia 55 0.090
43
c HYP836 Hypercholesterolemia, Familial, 1 73 0.084
44
TND005 Tendinitis 54 0.084
45
SBN001 Subendocardial Myocardial Infarction 22 0.084
46
P RHM011 Rheumatoid Arthritis 80 0.078
47
BRT054 Brittle Bone Disorder 72 0.078
48
P MYC007 Myocardial Infarction 70 0.078
49
OST017 Osteomyelitis 64 0.078
50
PSR001 Psoriatic Arthritis 61 0.078
51
SPN027 Spinal Stenosis 59 0.078
52
P MYS005 Myositis 56 0.078
53
PRC013 Pericarditis 54 0.078
54
MMM001 Mammary Paget's Disease 53 0.078
55
HYP025 Hyperphosphatemia 48 0.078
56
ART035 Arterial Calcification of Infancy 45 0.078
57
TNS014 Tenosynovitis 44 0.078
58
BCK006 Back Pain 42 0.078
59
SYN031 Synovial Chondromatosis 42 0.078
60
48X005 48,xyyy 39 0.078
61
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.078
62
P OST002 Osteoporosis 74 0.071
63
GTL001 Gitelman Syndrome 65 0.071
64
ALL026 Allergic Hypersensitivity Disease 62 0.071
65
P PLY019 Polyneuropathy 56 0.071
66
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.071
67
c HYP293 Hypophosphatasia, Adult 52 0.071
68
HYP014 Hyperuricemia 52 0.071
69
ENT004 Enthesopathy 49 0.071
70
URM002 Uremia 49 0.071
71
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.071
72
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.071
73
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.071
74
DSC004 Discitis 29 0.071
75
OLC001 Olecranon Bursitis 27 0.071
76
MYL069 Myeloma, Multiple 85 0.063
77
c SPN225 Spondyloarthropathy 1 73 0.063
78
P NRB001 Neuroblastoma 72 0.063
79
ACR007 Acromegaly 71 0.063
80
P SRC025 Sarcoidosis 1 70 0.063
81
P TMP003 Temporal Arteritis 68 0.063
82
P MYS003 Myasthenia Gravis 68 0.063
83
RCK004 Rickets 68 0.063
84
CRP001 Carpal Tunnel Syndrome 67 0.063
85
P HRP006 Herpes Simplex 65 0.063
86
LSH001 Leishmaniasis 63 0.063
87
HYP066 Hyperglycemia 61 0.063
88
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.063
89
c HYP292 Hypophosphatasia, Infantile 57 0.063
90
P NRP001 Neuropathy 56 0.063
91
NPH009 Nephrolithiasis 55 0.063
92
CRT017 Cartilage Disease 54 0.063
93
PLR008 Pleurisy 50 0.063
94
CRN030 Coronary Stenosis 50 0.063
95
TRY001 Trypanosomiasis 50 0.063
96
HLX001 Helix Syndrome 47 0.063
97
CRD137 Cardiogenic Shock 47 0.063
98
P KLZ004 Kala-Azar 1 41 0.063
99
CHL079 Children's Interstitial Lung Disease 26 0.063
100
c SYS001 Systemic Lupus Erythematosus 86 0.055
101
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.055
102
c ATR087 Atrial Standstill 1 75 0.055
103
HMN044 Human Immunodeficiency Virus Type 1 71 0.055
104
ADL002 Adult Syndrome 70 0.055
105
P MYP004 Myopathy 70 0.055
106
P MPL001 Maple Syrup Urine Disease 69 0.055
107
P SYS005 Systemic Scleroderma 68 0.055
108
CNN005 Connective Tissue Disease 68 0.055
109
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.055
110
OST159 Osteogenic Sarcoma 66 0.055
111
P MSC005 Muscular Dystrophy 66 0.055
113
OST003 Osteonecrosis 61 0.055
114
c SCL052 Scleroderma, Familial Progressive 61 0.055
115
CFF002 Coffin-Lowry Syndrome 60 0.055
116
P GLY013 Glycogen Storage Disease 60 0.055
117
P OPT006 Optic Nerve Disease 60 0.055
118
P MCR010 Microcephaly 59 0.055
119
P PRP019 Peripheral Nervous System Disease 58 0.055
120
P PLY041 Polymyositis 57 0.055
121
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.055
122
HYP266 Hypoxia 57 0.055
123
P HYP076 Hyperthyroidism 55 0.055
124
HRT012 Heart Valve Disease 53 0.055
125
P MNC007 Monocytic Leukemia 53 0.055
126
OST011 Osteomalacia 52 0.055
127
SPN051 Spondylitis 51 0.055
128
RDC002 Radiculopathy 50 0.055
129
WRN002 Wernicke-Korsakoff Syndrome 50 0.055
130
RNL011 Renal Osteodystrophy 50 0.055
131
47X002 47,xyy 49 0.055
132
HYP068 Hyperostosis 48 0.055
133
HYP596 Hypophosphatasia, Childhood 48 0.055
134
EXS001 Exostosis 46 0.055
135
MYS001 Myositis Ossificans 41 0.055
136
ANX004 Anoxia 40 0.055
137
HRW001 Hair Whorl 36 0.055
138
INF013 Inferior Myocardial Infarction 33 0.055
139
INF009 Inflammatory Spondylopathy 31 0.055
140
HYD003 Hydrarthrosis 31 0.055
141
c THM013 Thiamine Metabolism Dysfunction Syndrome 5 31 0.055
142
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 30 0.055
143
CLC004 Calcific Tendinitis 30 0.055
144
CRN264 Craniosynostosis with Fibular Aplasia 29 0.055
145
INT182 Intermittent Hydrarthrosis 18 0.055
146
c CHN021 Chondrocalcinosis 1 16 0.055
147
CYS001 Cystic Fibrosis 81 0.045
148
GLB015 Glioblastoma Multiforme 75 0.045
149
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.045
150
P OCL013 Oculodentodigital Dysplasia 69 0.045
151
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.045
152
P CRN037 Craniosynostosis 68 0.045
153
P LVR013 Liver Disease 68 0.045
154
P CRD119 Cardiac Arrest 67 0.045
155
ALC007 Alcohol Dependence 66 0.045
156
GLL008 Gilles De La Tourette Syndrome 66 0.045
157
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.045
158
TTN003 Tetanus 65 0.045
159
P GLM045 Glioma 63 0.045
160
P CRN300 Coronary Heart Disease 1 63 0.045
161
c GLY060 Glycogen Storage Disease Ia 63 0.045
162
LPP008 Lipoprotein Quantitative Trait Locus 62 0.045
163
LSC001 Lesch-Nyhan Syndrome 62 0.045
164
NTR005 Nutritional Deficiency Disease 62 0.045
165
P DRM010 Dermatomyositis 61 0.045
166
FTT001 Fatty Liver Disease 61 0.045
167
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 0.045
168
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 60 0.045
169
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.045
170
P SNS001 Sensorineural Hearing Loss 60 0.045
171
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.045
172
P MYC008 Myocarditis 59 0.045
173
PLM033 Pulmonary Embolism 59 0.045
174
HLC007 Helicobacter Pylori Infection 59 0.045
175
ANR040 Aneurysm 59 0.045
176
ISC004 Ischemia 58 0.045
177
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.045
178
P INF032 Infertility 57 0.045
179
P END033 Endocarditis 57 0.045
180
BCT022 Bacterial Infectious Disease 56 0.045
181
SFT003 Soft Tissue Sarcoma 56 0.045
182
P PRK001 Porokeratosis 55 0.045
183
P SPN052 Spondyloarthropathy 54 0.045
184
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.045
185
SLP001 Sleeping Sickness 54 0.045
186
GTR002 Goiter 53 0.045
187
DNT012 Dental Caries 53 0.045
188
ART140 Arteries, Anomalies of 52 0.045
189
NPH003 Nephrocalcinosis 51 0.045
190
OCL069 Ocular Motor Apraxia 51 0.045
191
c SCN007 Secondary Hyperparathyroidism 51 0.045
192
c INF145 Infantile Liver Failure Syndrome 1 50 0.045
193
DYS073 Dysphagia 50 0.045
194
HYP017 Hypophosphatemia 50 0.045
195
LFT001 Left Bundle Branch Hemiblock 49 0.045
196
VCC001 Vaccinia 49 0.045
197
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 47 0.045
198
MCR018 Microcytic Anemia 47 0.045
199
IRN004 Iron-Refractory Iron Deficiency Anemia 47 0.045
200
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.045
201
SPN020 Spondylosis 46 0.045
202
GLL048 Glial Tumor 45 0.045
203
c HRD039 Hereditary Amyloidosis 45 0.045
204
HMR002 Hemarthrosis 45 0.045
205
SPS057 Spasticity 45 0.045
206
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.045
207
GNG003 Gingival Recession 44 0.045
208
CHN010 Chondroma 43 0.045
209
TND004 Tendinopathy 43 0.045
210
ANC001 Ancylostomiasis 43 0.045
211
P HYP265 Hypotonia 43 0.045
212
CNS002 Constrictive Pericarditis 40 0.045
213
P TRC031 Trichorhinophalangeal Syndrome 40 0.045
214
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.045
215
PRM329 Premature Aging 35 0.045
216
MCR257 Microcephaly, Amish Type 34 0.045
217
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.045
218
c PRG106 Progressive Muscular Dystrophy 33 0.045
219
PRR001 Periarthritis 32 0.045
221
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.045
222
c GLY017 Glycogen Storage Disease Ic 30 0.045
223
ARG004 Argyria 27 0.045
224
P HPT023 Hepatocellular Carcinoma 100 0.032
225
P PRS040 Prostate Cancer 97 0.032
226
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.032
227
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.032
228
c HYP595 Hypertension, Essential 84 0.032
229
P PNC035 Pancreatic Cancer 84 0.032
230
P GST053 Gastric Cancer 83 0.032
231
P ATX030 Ataxia-Telangiectasia 82 0.032
232
P LKM071 Leukemia, Chronic Lymphocytic 79 0.032
233
INS024 Insulin-Like Growth Factor I 79 0.032
234
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.032
235
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.032
236
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.032
237
c HPT073 Hepatitis C Virus 72 0.032
238
WLS001 Wilson Disease 71 0.032
239
MYL009 Myelodysplastic Syndrome 70 0.032
240
DWN001 Down Syndrome 70 0.032
241
LGH007 Leigh Syndrome 70 0.032
242
P OST001 Osteopetrosis 70 0.032
243
P ASP006 Aspergillosis 69 0.032
244
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.032
245
PLM001 Pulmonary Tuberculosis 69 0.032
246
ART016 Aortic Aneurysm 69 0.032
247
P ANG001 Angelman Syndrome 69 0.032
248
P MYC084 Mycobacterium Tuberculosis 1 68 0.032
249
CHL065 Cholangiocarcinoma 68 0.032
250
CRZ001 Crouzon Syndrome 68 0.032
251
P INF038 Influenza 68 0.032
252
BRK010 Burkitt Lymphoma 67 0.032
253
CRB039 Cerebrovascular Disease 67 0.032
254
P TRN020 Turner Syndrome 67 0.032
255
P HYP098 Hypereosinophilic Syndrome 67 0.032
256
P PLM037 Pulmonary Hypertension 67 0.032
257
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.032
258
P MLG056 Malignant Hyperthermia 67 0.032
259
c RHB024 Rhabdomyosarcoma 2 67 0.032
260
P MCR115 Microvascular Complications of Diabetes 5 66 0.032
261
c MCR129 Microvascular Complications of Diabetes 1 66 0.032
262
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.032
263
ART001 Arterial Tortuosity Syndrome 66 0.032
264
AND002 Androgen Insensitivity Syndrome 66 0.032
265
P DYS154 Dystonia 65 0.032
266
SRC014 Sarcoma 65 0.032
267
PPL049 Papillon-Lefevre Syndrome 65 0.032
268
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.032
269
TNG002 Tangier Disease 65 0.032
270
BRR014 Barrett Esophagus 65 0.032
271
PRT037 Pertussis 65 0.032
272
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.032
273
P DBT009 Diabetes Mellitus 64 0.032
274
NRM005 Neuromuscular Disease 64 0.032
275
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.032
276
c JVN010 Juvenile Rheumatoid Arthritis 64 0.032
277
ART002 Arts Syndrome 64 0.032
278
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.032
279
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.032
280
MSC007 Muscle Hypertrophy 64 0.032
281
P ADN016 Adenocarcinoma 64 0.032
282
LYM017 Lyme Disease 64 0.032
283
P NTR004 Neutropenia 63 0.032
284
P ANR048 Aniridia 1 63 0.032
285
P VSC007 Vascular Disease 63 0.032
286
c HYP794 Hyperoxaluria, Primary, Type I 63 0.032
287
c MLG084 Malignant Fibrous Histiocytoma 63 0.032
288
c ACT068 Acute Cystitis 63 0.032
289
ANR007 Anorexia Nervosa 63 0.032
290
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.032
291
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.032
292
c FNC043 Fanconi Anemia, Complementation Group E 62 0.032
293
c HPT001 Hepatitis C 62 0.032
294
c GLY004 Glycogen Storage Disease V 62 0.032
295
P TRC086 Trichohepatoenteric Syndrome 1 62 0.032
296
P ACR001 Aicardi-Goutieres Syndrome 62 0.032
297
CTN007 Cutaneous Leishmaniasis 62 0.032
298
P OST009 Osteochondritis Dissecans 62 0.032
299
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.032
300
c PNS012 Paine Syndrome 61 0.032
301
P ENC018 Encephalopathy 61 0.032
302
RCT015 Reactive Arthritis 61 0.032
303
P PNC044 Pancreatitis 61 0.032
304
P LPS004 Lupus Erythematosus 61 0.032
305
P HMN010 Hemangioma 61 0.032
306
P KDN017 Kidney Cancer 60 0.032
307
c JVN061 Juvenile Arthritis 60 0.032
308
P SCL018 Scoliosis 60 0.032
309
P TXP001 Toxoplasmosis 60 0.032
310
c ACT027 Acute Pancreatitis 60 0.032
311
ACN002 Acanthosis Nigricans 60 0.032
312
SQM006 Squamous Cell Carcinoma 60 0.032
313
RHM001 Rheumatic Fever 60 0.032
314
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.032
315
P CTR002 Cataract 60 0.032
316
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.032
317
c ACT071 Acute Kidney Failure 60 0.032
318
SPP011 Suppression of Tumorigenicity 12 59 0.032
319
P AXN002 Axenfeld-Rieger Syndrome 59 0.032
320
c HPT016 Hepatitis B 59 0.032
321
P BRS044 Breast Adenocarcinoma 59 0.032
322
GNG013 Gingivitis 59 0.032
323
P NMN002 Niemann-Pick Disease 59 0.032
324
ADN018 Adenoma 59 0.032
325
SRC027 Sarcoma, Synovial 58 0.032
326
INC002 Inclusion Body Myositis 58 0.032
327
ALK013 Alkaptonuria 58 0.032
328
ANT024 Anthrax Disease 58 0.032
329
P HYP726 Hypercalcemia, Infantile, 1 58 0.032
330
P PGT001 Paget's Disease of Bone 58 0.032
331
FBR047 Fibromyalgia 58 0.032
332
P BNC003 Bone Cancer 58 0.032
333
P UVT001 Uveitis 57 0.032
334
P GLM007 Glomerulonephritis 57 0.032
335
P ZLL001 Zellweger Syndrome 57 0.032
336
c ANM036 Anemia, Sideroblastic, 1 57 0.032
337
P EXN002 Exanthem 57 0.032
338
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.032
339
CYT008 Cytomegalovirus Infection 57 0.032
340
ENC044 Enchondromatosis, Multiple, Ollier Type 57 0.032
341
P PYL005 Pyelonephritis 56 0.032
342
c ACT134 Acute Liver Failure 56 0.032
343
SPN041 Spinal Cord Disease 56 0.032
344
ISL001 Islet Cell Tumor 56 0.032
345
P PSD015 Pseudohypoparathyroidism 56 0.032
346
GST050 Gastrointestinal System Disease 56 0.032
347
P HYP024 Hypoparathyroidism 56 0.032
348
P RST002 Restrictive Cardiomyopathy 56 0.032
349
AGN016 Aging 56 0.032
350
P GST044 Gastritis 56 0.032
351
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.032
352
LMB062 Limb Ischemia 55 0.032
353
c OST135 Osteogenesis Imperfecta, Type I 55 0.032
354
P MLN007 Male Infertility 55 0.032
355
P DRR001 Diarrhea 55 0.032
356
ACT058 Active Peptic Ulcer Disease 55 0.032
357
P ALP106 Alport Syndrome 1, X-Linked 55 0.032
358
HMP005 Hemiplegia 55 0.032
359
GNT003 Genital Herpes 54 0.032
360
HYP060 Hyperinsulinism 54 0.032
361
ADN024 Adenine Phosphoribosyltransferase Deficiency 54 0.032
362
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.032
363
THR013 Thoracic Outlet Syndrome 54 0.032
364
PLM010 Pulmonary Edema 54 0.032
365
P LTR001 Lateral Sclerosis 54 0.032
366
HMS001 Hemosiderosis 54 0.032
367
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.032
368
OST016 Osteochondrosis 53 0.032
369
INF034 Infective Endocarditis 53 0.032
370
P SHR001 Short Bowel Syndrome 53 0.032
371
INT075 Intracranial Hypertension 53 0.032
372
SPN035 Spindle Cell Sarcoma 53 0.032
373
PRP016 Paraplegia 52 0.032
374
P BRT004 Bartter Disease 52 0.032
375
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.032
376
c VRL005 Viral Pneumonia 52 0.032
377
MGL001 Megaloblastic Anemia 51 0.032
378
CLC001 Calciphylaxis 51 0.032
379
SPN019 Spondylolisthesis 51 0.032
380
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 51 0.032
381
HYP781 Hypoascorbemia 51 0.032
382
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.032
383
c ALM001 Al Amyloidosis 50 0.032
384
PRT029 Parathyroid Adenoma 50 0.032
385
BRX001 Bruxism 50 0.032
386
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.032
387
FSC004 Fasciitis 50 0.032
388
DBT004 Diabetic Polyneuropathy 49 0.032
389
RBF001 Riboflavin Deficiency 49 0.032
390
P CRV039 Cervicitis 49 0.032
391
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.032
392
MNN009 Meningoencephalitis 49 0.032
393
QDR001 Quadriplegia 48 0.032
394
WTH001 Withdrawal Disorder 48 0.032
395
RCT020 Rectum Adenocarcinoma 48 0.032
396
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.032
397
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.032
398
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.032
399
CHR074 Choriocarcinoma 47 0.032
400
c ACT076 Acute Myocarditis 46 0.032
401
MYC005 Myocardial Stunning 46 0.032
402
EXT033 Extrapulmonary Tuberculosis 46 0.032
403
MLK003 Melkersson-Rosenthal Syndrome 45 0.032
404
SBC016 Subacute Delirium 44 0.032
405
c PCH010 Pachyonychia Congenita 3 44 0.032
406
DWR001 Dwarfism 44 0.032
407
AGG012 Aggressive Nk-Cell Leukemia 44 0.032
408
SPN119 Spondylarthropathy 44 0.032
409
FBR054 Fibroma 44 0.032
410
FNG004 Fungal Meningitis 44 0.032
411
MND023 Mend Syndrome 43 0.032
412
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.032
413
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 0.032
414
MDD018 Middle East Respiratory Syndrome 43 0.032
415
HMP009 Haemophilus Influenzae 43 0.032
416
P AVS003 Avascular Necrosis 42 0.032
417
ALC010 Alcoholic Cardiomyopathy 42 0.032
418
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.032
419
ATX019 Ataxia with Vitamin E Deficiency 42 0.032
420
OBS082 Obstructive Nephropathy 42 0.032
421
PYM001 Pyomyositis 41 0.032
422
PRS063 Paresthesia 41 0.032
423
RDN001 Reading Disorder 40 0.032
424
CLD014 Cole Disease 40 0.032
425
CHN004 Chondroblastoma 40 0.032
426
NRV004 Nerve Compression Syndrome 40 0.032
427
TNS001 Tenosynovial Giant Cell Tumor 40 0.032
428
DSS010 Dissociative Disorder 39 0.032
429
OCH001 Ochronosis 38 0.032
430
HYP001 Hypochromic Microcytic Anemia 38 0.032
431
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.032
432
CRD016 Cardiac Rupture 37 0.032
433
HMN004 Hemangioma of Liver 36 0.032
434
EPD005 Epidural Abscess 35 0.032
435
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 35 0.032
436
ATX010 Ataxia Neuropathy Spectrum 34 0.032
437
c LKM005 Leukemia, T-Cell, Chronic 34 0.032
438
HMP018 Hemophilic Arthropathy 34 0.032
439
PPL052 Papillomatosis, Confluent and Reticulated 33 0.032
440
SPN029 Spondylolysis 33 0.032
441
FTD001 Foot Drop 33 0.032
442
BNN005 Bunion 33 0.032
443
ALR002 Al-Raqad Syndrome 33 0.032
444
ULN001 Ulnar Neuropathy 33 0.032
445
ACT064 Acute Necrotizing Encephalitis 33 0.032
446
KDN013 Kidney Hypertrophy 32 0.032
447
PLN007 Plantar Fasciitis 32 0.032
448
CYT004 Cytomegalic Inclusion Disease 31 0.032
449
TTH007 Tooth Erosion 31 0.032
450
SPN392 Spondylosis, Cervical 30 0.032
451
PYR016 Pyridoxine Deficiency 30 0.032
452
MYC088 Mycobacterium Avium Complex Infections 29 0.032
453
P SKL032 Skeletal Muscle Disease 29 0.032
454
PST092 Posttransplant Acute Limbic Encephalitis 29 0.032
455
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.032
456
VLK001 Volkmann Contracture 25 0.032
457
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.032
458
CLC064 Calcifying Aponeurotic Fibroma 23 0.032
459
c GLC079 Glaucoma 1, Open Angle, P 23 0.032
460
MSC148 Musical Perfect Pitch 22 0.032
461
PRD026 Pre-Descemet Corneal Dystrophy 21 0.032
462
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.032
463
AND005 Androgen Insensitivity Syndrome, Mild 19 0.032
464
EXT012 Extraskeletal Chondroma 19 0.032
465
LTR004 Lateral Myocardial Infarction 19 0.032
466
WLF014 Wolfram Syndrome, Mitochondrial Form 17 0.032
467
c SYS048 Systemic Lupus Erythematosus 8 17 0.032
468
BLD137 Blood Group--Ahonen 16 0.032
469
c CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 15 0.032
470
c OPT071 Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive 14 0.032
471
NRL025 Neural Tube Closure Defect 12 0.032
472
DFN002 Dfnx1 Nonsyndromic Hearing Loss and Deafness 8 0.032
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