Search results for pyrophosphate

474 hits were found for pyrophosphate

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 35 9.141
2
FML307 Familial Calcium Pyrophosphate Deposition 38 6.951
3
P CHN059 Chondrocalcinosis 51 4.564
4
P ART023 Arthropathy 61 0.403
5
GT001 Gout 63 0.286
6
c ACT075 Acute Myocardial Infarction 59 0.271
7
OST012 Osteoarthritis 80 0.236
8
IRN002 Iron Metabolism Disease 58 0.223
9
P HYP069 Hyperparathyroidism 64 0.198
10
P AMY004 Amyloidosis 71 0.195
11
P KDN018 Kidney Disease 73 0.182
12
c CHR684 Chronic Kidney Disease 68 0.179
13
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.179
14
BNR002 Bone Resorption Disease 51 0.176
15
SYN007 Synovitis 55 0.170
16
END030 End Stage Renal Failure 60 0.167
17
P HYP035 Hypophosphatasia 58 0.167
18
P MYC007 Myocardial Infarction 74 0.154
19
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.154
20
INT007 Intermediate Coronary Syndrome 58 0.151
21
ANK001 Ankylosis 51 0.151
22
DFC004 Deficiency Anemia 77 0.140
23
c HMC039 Hemochromatosis, Type 1 73 0.140
24
P ART022 Arthritis 71 0.140
25
CRY024 Crystal Arthropathies 21 0.132
26
ANG054 Angina Pectoris 66 0.129
27
P BRB001 Beriberi 41 0.116
28
P HYP086 Hypothyroidism 70 0.111
29
SPT004 Septic Arthritis 55 0.107
30
IRN001 Iron Deficiency Anemia 59 0.102
31
CLC006 Calcinosis 48 0.102
32
c KNN009 Kenny-Caffey Syndrome, Type 1 33 0.102
33
P RHM011 Rheumatoid Arthritis 82 0.096
34
CNG034 Congestive Heart Failure 69 0.096
35
CHG001 Chagas Disease 66 0.091
36
BND020 Bone Disease 60 0.091
37
c PRM005 Primary Hyperparathyroidism 60 0.091
38
P CHN012 Chondrosarcoma 57 0.091
39
HYP005 Hypokalemia 55 0.091
40
FRZ001 Frozen Shoulder 53 0.091
41
BRS064 Bursitis 42 0.091
42
c HYP836 Hypercholesterolemia, Familial, 1 74 0.085
43
P PSD087 Pseudoxanthoma Elasticum 67 0.085
44
TND005 Tendinitis 45 0.085
45
BCK006 Back Pain 44 0.085
46
SBN001 Subendocardial Myocardial Infarction 31 0.085
47
P OST002 Osteoporosis 79 0.079
48
BRT054 Brittle Bone Disorder 71 0.079
49
OST017 Osteomyelitis 65 0.079
50
ISC004 Ischemia 62 0.079
51
SPN027 Spinal Stenosis 58 0.079
52
PRC013 Pericarditis 54 0.079
53
P MYS005 Myositis 54 0.079
54
MMM001 Mammary Paget's Disease 53 0.079
55
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.079
56
HYP025 Hyperphosphatemia 47 0.079
57
ART035 Arterial Calcification of Infancy 44 0.079
58
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.079
60
MYL069 Myeloma, Multiple 85 0.072
61
ALL026 Allergic Hypersensitivity Disease 65 0.072
62
PSR001 Psoriatic Arthritis 63 0.072
63
GTL001 Gitelman Syndrome 62 0.072
64
RHM027 Rheumatic Disease 56 0.072
65
c HYP293 Hypophosphatasia, Adult 56 0.072
66
P PLY019 Polyneuropathy 55 0.072
67
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.072
68
HYP014 Hyperuricemia 52 0.072
69
URM002 Uremia 50 0.072
70
ENT004 Enthesopathy 46 0.072
71
SYN031 Synovial Chondromatosis 43 0.072
72
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.072
73
48X005 48,xyyy 37 0.072
74
TNS014 Tenosynovitis 37 0.072
75
OLC001 Olecranon Bursitis 29 0.072
76
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.064
77
c SPN225 Spondyloarthropathy 1 74 0.064
78
P SRC025 Sarcoidosis 1 72 0.064
79
ACR007 Acromegaly 70 0.064
80
RCK004 Rickets 70 0.064
81
P MYS003 Myasthenia Gravis 68 0.064
82
CRP001 Carpal Tunnel Syndrome 68 0.064
83
P HRP006 Herpes Simplex 66 0.064
84
LSH001 Leishmaniasis 64 0.064
85
HYP066 Hyperglycemia 63 0.064
86
ADL002 Adult Syndrome 62 0.064
87
P NRP001 Neuropathy 57 0.064
88
c HYP292 Hypophosphatasia, Infantile 54 0.064
89
CRT017 Cartilage Disease 54 0.064
90
PLR008 Pleurisy 50 0.064
91
CRD137 Cardiogenic Shock 50 0.064
92
CRN030 Coronary Stenosis 49 0.064
93
P KLZ004 Kala-Azar 1 43 0.064
94
DSC004 Discitis 30 0.064
95
CHL079 Children's Interstitial Lung Disease 27 0.064
96
c SYS001 Systemic Lupus Erythematosus 88 0.056
97
c ATR087 Atrial Standstill 1 76 0.056
98
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.056
99
HMN044 Human Immunodeficiency Virus Type 1 73 0.056
100
P SYS005 Systemic Scleroderma 68 0.056
101
P TMP003 Temporal Arteritis 68 0.056
102
CNN005 Connective Tissue Disease 68 0.056
103
P MPL001 Maple Syrup Urine Disease 68 0.056
104
P MSC005 Muscular Dystrophy 68 0.056
105
P CRN018 Coronary Artery Anomaly 67 0.056
106
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.056
107
P NRB010 Neuroblastoma 1 66 0.056
108
P PRP019 Peripheral Nervous System Disease 64 0.056
109
P MYP004 Myopathy 63 0.056
110
OST003 Osteonecrosis 62 0.056
111
c SCL052 Scleroderma, Familial Progressive 62 0.056
112
NTR005 Nutritional Deficiency Disease 61 0.056
113
ANR040 Aneurysm 60 0.056
114
P CRN300 Coronary Heart Disease 1 59 0.056
115
P OPT006 Optic Nerve Disease 59 0.056
116
P GLY013 Glycogen Storage Disease 59 0.056
118
CFF002 Coffin-Lowry Syndrome 57 0.056
119
P PLY041 Polymyositis 57 0.056
120
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.056
121
P MCR010 Microcephaly 56 0.056
122
HRT012 Heart Valve Disease 56 0.056
123
P HYP076 Hyperthyroidism 55 0.056
124
SPN051 Spondylitis 53 0.056
125
P MNC007 Monocytic Leukemia 52 0.056
126
OST011 Osteomalacia 51 0.056
127
RDC002 Radiculopathy 51 0.056
128
RNL011 Renal Osteodystrophy 49 0.056
129
47X002 47,xyy 49 0.056
130
HYP068 Hyperostosis 48 0.056
131
WRN002 Wernicke-Korsakoff Syndrome 48 0.056
132
HLX001 Helix Syndrome 46 0.056
133
EXS001 Exostosis 46 0.056
134
ANX004 Anoxia 44 0.056
135
HYP596 Hypophosphatasia, Childhood 42 0.056
136
MYS001 Myositis Ossificans 38 0.056
137
HYD003 Hydrarthrosis 37 0.056
138
HRW001 Hair Whorl 36 0.056
139
CLC004 Calcific Tendinitis 36 0.056
140
INF013 Inferior Myocardial Infarction 35 0.056
141
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 32 0.056
142
INF009 Inflammatory Spondylopathy 29 0.056
143
CRN264 Craniosynostosis with Fibular Aplasia 27 0.056
144
INT182 Intermittent Hydrarthrosis 19 0.056
145
c CHN021 Chondrocalcinosis 1 16 0.056
146
P OBS848 Obsolete: Familial Articular Chondrocalcinosis Type 2 6 0.056
147
CYS001 Cystic Fibrosis 84 0.045
148
GLB002 Glioblastoma 74 0.045
149
PRP027 Peripheral Vascular Disease 72 0.045
150
P LVR013 Liver Disease 71 0.045
151
P CRD119 Cardiac Arrest 71 0.045
152
P CRN037 Craniosynostosis 69 0.045
153
ALC007 Alcohol Dependence 68 0.045
154
OST159 Osteogenic Sarcoma 67 0.045
155
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.045
156
GLL008 Gilles De La Tourette Syndrome 66 0.045
157
P OCL013 Oculodentodigital Dysplasia 65 0.045
158
P ADN016 Adenocarcinoma 65 0.045
159
HTC003 Hutchinson-Gilford Progeria Syndrome 64 0.045
160
P GLM045 Glioma 64 0.045
161
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.045
162
c GLY060 Glycogen Storage Disease Ia 63 0.045
163
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.045
164
TTN003 Tetanus 62 0.045
165
P SNS001 Sensorineural Hearing Loss 62 0.045
166
P DRM010 Dermatomyositis 62 0.045
167
HLC007 Helicobacter Pylori Infection 61 0.045
168
LSC001 Lesch-Nyhan Syndrome 61 0.045
169
GLB015 Glioblastoma Multiforme 60 0.045
170
P MYC008 Myocarditis 60 0.045
171
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.045
172
PLM033 Pulmonary Embolism 60 0.045
173
ART140 Arteries, Anomalies of 60 0.045
174
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.045
175
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 59 0.045
176
P END033 Endocarditis 58 0.045
177
HYP266 Hypoxia 58 0.045
178
AGN016 Aging 58 0.045
179
BCT022 Bacterial Infectious Disease 57 0.045
180
SFT003 Soft Tissue Sarcoma 57 0.045
181
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.045
182
ACT058 Active Peptic Ulcer Disease 55 0.045
183
P SPN052 Spondyloarthropathy 54 0.045
184
GTR002 Goiter 54 0.045
185
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 53 0.045
186
OCL069 Ocular Motor Apraxia 53 0.045
187
DYS073 Dysphagia 52 0.045
188
DNT012 Dental Caries 52 0.045
189
c SCN007 Secondary Hyperparathyroidism 52 0.045
190
P FML068 Familial Hypocalciuric Hypercalcemia 50 0.045
191
VCC001 Vaccinia 50 0.045
192
TRY001 Trypanosomiasis 50 0.045
193
c INF145 Infantile Liver Failure Syndrome 1 50 0.045
194
GLL048 Glial Tumor 48 0.045
195
HYP017 Hypophosphatemia 48 0.045
196
SPN020 Spondylosis 48 0.045
197
LFT001 Left Bundle Branch Hemiblock 47 0.045
198
MCR018 Microcytic Anemia 46 0.045
199
HMR002 Hemarthrosis 46 0.045
200
IRN004 Iron-Refractory Iron Deficiency Anemia 45 0.045
201
TND004 Tendinopathy 44 0.045
202
CHN010 Chondroma 44 0.045
203
GNG003 Gingival Recession 43 0.045
204
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 42 0.045
205
P TRC031 Trichorhinophalangeal Syndrome 41 0.045
206
PRM329 Premature Aging 41 0.045
207
ANC001 Ancylostomiasis 39 0.045
208
SPS057 Spasticity 38 0.045
209
CNS002 Constrictive Pericarditis 37 0.045
210
c PRG106 Progressive Muscular Dystrophy 34 0.045
211
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.045
212
MCR257 Microcephaly, Amish Type 33 0.045
213
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.045
215
PRR001 Periarthritis 30 0.045
216
ANK010 Ankylostomiasis 30 0.045
217
c GLY017 Glycogen Storage Disease Ic 29 0.045
218
ARG004 Argyria 28 0.045
219
c THM013 Thiamine Metabolism Dysfunction Syndrome 5 26 0.045
220
c OBS847 Obsolete: Familial Articular Chondrocalcinosis Type 1 7 0.045
221
P HPT023 Hepatocellular Carcinoma 99 0.032
222
P PRS040 Prostate Cancer 97 0.032
223
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.032
224
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.032
225
c HYP595 Hypertension, Essential 87 0.032
226
P GST053 Gastric Cancer 85 0.032
227
P ATX030 Ataxia-Telangiectasia 83 0.032
228
c LKM071 Leukemia, Chronic Lymphocytic 81 0.032
229
INS024 Insulin-Like Growth Factor I 79 0.032
230
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.032
231
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.032
232
P HRT032 Heart Disease 78 0.032
233
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.032
234
c HPT073 Hepatitis C Virus 74 0.032
235
c LKM063 Leukemia, Chronic Myeloid 74 0.032
236
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.032
237
PLM001 Pulmonary Tuberculosis 72 0.032
238
MYL009 Myelodysplastic Syndrome 72 0.032
239
ART016 Aortic Aneurysm 71 0.032
240
DWN001 Down Syndrome 70 0.032
241
P OST001 Osteopetrosis 70 0.032
242
WLS001 Wilson Disease 69 0.032
243
P PLM037 Pulmonary Hypertension 69 0.032
244
P MYC084 Mycobacterium Tuberculosis 1 69 0.032
245
P INF038 Influenza 69 0.032
246
LGH007 Leigh Syndrome 69 0.032
247
P LKM002 Leukemia 69 0.032
248
CHL065 Cholangiocarcinoma 68 0.032
249
BRK010 Burkitt Lymphoma 68 0.032
250
P MCR115 Microvascular Complications of Diabetes 5 67 0.032
251
c JVN010 Juvenile Rheumatoid Arthritis 67 0.032
252
P HYP098 Hypereosinophilic Syndrome 67 0.032
253
CRZ001 Crouzon Syndrome 67 0.032
254
SRC014 Sarcoma 67 0.032
255
P ASP006 Aspergillosis 67 0.032
256
c MCR129 Microvascular Complications of Diabetes 1 67 0.032
257
BRR014 Barrett Esophagus 67 0.032
258
P DBT009 Diabetes Mellitus 66 0.032
259
PRT037 Pertussis 66 0.032
260
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.032
261
AND002 Androgen Insensitivity Syndrome 66 0.032
262
INC002 Inclusion Body Myositis 66 0.032
263
P TRN020 Turner Syndrome 66 0.032
264
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.032
265
P VSC007 Vascular Disease 65 0.032
266
P DYS154 Dystonia 65 0.032
267
P ANG001 Angelman Syndrome 65 0.032
268
MSC007 Muscle Hypertrophy 65 0.032
269
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.032
270
FBR011 Fibrodysplasia Ossificans Progressiva 65 0.032
271
TNG002 Tangier Disease 64 0.032
272
ANR007 Anorexia Nervosa 64 0.032
273
LYM017 Lyme Disease 64 0.032
274
c RHB024 Rhabdomyosarcoma 2 64 0.032
275
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.032
276
P ENC018 Encephalopathy 64 0.032
277
P NTR004 Neutropenia 64 0.032
278
P ANR048 Aniridia 1 64 0.032
279
c ACT068 Acute Cystitis 63 0.032
280
c HPT016 Hepatitis B 63 0.032
281
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.032
282
PPL049 Papillon-Lefevre Syndrome 63 0.032
283
P ACR001 Aicardi-Goutieres Syndrome 63 0.032
284
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.032
285
FTT001 Fatty Liver Disease 63 0.032
286
P LPS004 Lupus Erythematosus 62 0.032
287
NRM005 Neuromuscular Disease 62 0.032
288
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.032
289
c HPT001 Hepatitis C 62 0.032
290
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.032
291
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.032
292
ACN002 Acanthosis Nigricans 62 0.032
293
P CTR002 Cataract 62 0.032
294
c PNS012 Paine Syndrome 61 0.032
295
CTN007 Cutaneous Leishmaniasis 61 0.032
296
P TXP001 Toxoplasmosis 61 0.032
297
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.032
298
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 61 0.032
299
P SCL018 Scoliosis 61 0.032
300
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.032
301
SQM006 Squamous Cell Carcinoma 60 0.032
302
P NMN002 Niemann-Pick Disease 60 0.032
303
GNG013 Gingivitis 60 0.032
304
c ACT027 Acute Pancreatitis 60 0.032
305
ART001 Arterial Tortuosity Syndrome 60 0.032
306
c ACT071 Acute Kidney Failure 60 0.032
307
FBR047 Fibromyalgia 60 0.032
308
P KDN017 Kidney Cancer 60 0.032
309
c GLY004 Glycogen Storage Disease V 60 0.032
310
SRC027 Sarcoma, Synovial 60 0.032
311
P MLG056 Malignant Hyperthermia 60 0.032
312
ADN018 Adenoma 60 0.032
313
P OST009 Osteochondritis Dissecans 60 0.032
314
P INF032 Infertility 60 0.032
315
P BRS044 Breast Adenocarcinoma 59 0.032
316
P PGT001 Paget's Disease of Bone 59 0.032
317
P OST135 Osteogenesis Imperfecta, Type I 59 0.032
318
P GLM007 Glomerulonephritis 58 0.032
319
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.032
320
P UVT001 Uveitis 58 0.032
321
CYT008 Cytomegalovirus Infection 58 0.032
322
P HYP726 Hypercalcemia, Infantile, 1 58 0.032
323
P AXN002 Axenfeld-Rieger Syndrome 58 0.032
324
RCT015 Reactive Arthritis 58 0.032
325
P EXN002 Exanthem 58 0.032
326
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.032
327
P PYL005 Pyelonephritis 58 0.032
328
P GST044 Gastritis 58 0.032
329
P TRC086 Trichohepatoenteric Syndrome 1 57 0.032
330
ALK013 Alkaptonuria 57 0.032
331
SPN041 Spinal Cord Disease 57 0.032
332
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.032
333
SPN035 Spindle Cell Sarcoma 57 0.032
334
ANT024 Anthrax Disease 56 0.032
335
c ANM036 Anemia, Sideroblastic, 1 56 0.032
336
P BNC003 Bone Cancer 56 0.032
337
P LYM031 Lymphocytic Leukemia 56 0.032
338
P ZLL001 Zellweger Syndrome 56 0.032
339
P BRT004 Bartter Disease 56 0.032
340
RHM001 Rheumatic Fever 56 0.032
341
P LTR001 Lateral Sclerosis 56 0.032
342
P HYP024 Hypoparathyroidism 56 0.032
343
PLM010 Pulmonary Edema 56 0.032
344
P RST002 Restrictive Cardiomyopathy 55 0.032
345
P ALP106 Alport Syndrome 1, X-Linked 55 0.032
346
P DRR001 Diarrhea 55 0.032
347
HMP005 Hemiplegia 55 0.032
348
OST016 Osteochondrosis 55 0.032
349
P PSD015 Pseudohypoparathyroidism 54 0.032
350
PRP016 Paraplegia 54 0.032
351
GNT003 Genital Herpes 54 0.032
352
INT075 Intracranial Hypertension 54 0.032
353
PLM017 Pulmonary Alveolar Microlithiasis 54 0.032
354
HMS001 Hemosiderosis 54 0.032
355
P MGL001 Megaloblastic Anemia 54 0.032
356
SPN019 Spondylolisthesis 54 0.032
357
INF034 Infective Endocarditis 53 0.032
358
ENC044 Enchondromatosis, Multiple, Ollier Type 53 0.032
359
c ACR116 Aicardi-Goutieres Syndrome 1 53 0.032
360
c ACT134 Acute Liver Failure 53 0.032
361
NPH003 Nephrocalcinosis 52 0.032
362
ADN024 Adenine Phosphoribosyltransferase Deficiency 52 0.032
363
PRT029 Parathyroid Adenoma 52 0.032
364
P CHR345 Chronic Pain 52 0.032
365
QDR001 Quadriplegia 51 0.032
366
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.032
367
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 51 0.032
368
c ALM001 Al Amyloidosis 50 0.032
369
LMB062 Limb Ischemia 50 0.032
370
P SHR001 Short Bowel Syndrome 50 0.032
371
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.032
372
MNN009 Meningoencephalitis 50 0.032
373
MLK003 Melkersson-Rosenthal Syndrome 50 0.032
374
P IDP024 Idiopathic Inflammatory Myopathy 49 0.032
375
BRX001 Bruxism 49 0.032
376
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.032
377
CLC001 Calciphylaxis 49 0.032
378
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 49 0.032
379
THR013 Thoracic Outlet Syndrome 49 0.032
380
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.032
381
HYP781 Hypoascorbemia 48 0.032
382
P TCL004 T-Cell Leukemia 48 0.032
383
DBT004 Diabetic Polyneuropathy 48 0.032
384
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.032
385
c HYP794 Hyperoxaluria, Primary, Type I 48 0.032
386
WTH001 Withdrawal Disorder 47 0.032
387
SLP001 Sleeping Sickness 47 0.032
388
CHR074 Choriocarcinoma 47 0.032
389
FSC004 Fasciitis 47 0.032
390
ISL001 Islet Cell Tumor 47 0.032
391
CYT002 Cytokine Deficiency 46 0.032
392
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.032
393
HMP009 Haemophilus Influenzae 46 0.032
394
EXT033 Extrapulmonary Tuberculosis 46 0.032
395
LCK001 Locked-in Syndrome 46 0.032
396
PRS063 Paresthesia 46 0.032
397
RBF001 Riboflavin Deficiency 46 0.032
398
ATX019 Ataxia with Vitamin E Deficiency 46 0.032
399
c ACT076 Acute Myocarditis 45 0.032
400
DWR001 Dwarfism 45 0.032
401
MYC005 Myocardial Stunning 45 0.032
402
SPN119 Spondylarthropathy 45 0.032
403
P GNT008 Giant Cell Tumor 45 0.032
404
FBR054 Fibroma 45 0.032
405
HYP706 Hypermobile Ehlers-Danlos Syndrome 44 0.032
406
NTR003 Natural Killer Cell Leukemia 44 0.032
407
OBS082 Obstructive Nephropathy 44 0.032
408
c PCH010 Pachyonychia Congenita 3 43 0.032
409
P AVS003 Avascular Necrosis 43 0.032
410
P HYP265 Hypotonia 43 0.032
411
SBC016 Subacute Delirium 43 0.032
412
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.032
413
ALC010 Alcoholic Cardiomyopathy 42 0.032
414
P CRV039 Cervicitis 42 0.032
415
c VRL005 Viral Pneumonia 42 0.032
416
MND023 Mend Syndrome 42 0.032
417
RDN001 Reading Disorder 42 0.032
418
CLD014 Cole Disease 41 0.032
419
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 41 0.032
420
PYM001 Pyomyositis 41 0.032
421
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.032
422
SPN029 Spondylolysis 39 0.032
423
RCT020 Rectum Adenocarcinoma 39 0.032
424
ATX010 Ataxia Neuropathy Spectrum 39 0.032
425
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.032
426
HYP001 Hypochromic Microcytic Anemia 38 0.032
427
FNG004 Fungal Meningitis 37 0.032
428
TNS001 Tenosynovial Giant Cell Tumor 36 0.032
429
OCH001 Ochronosis 36 0.032
430
HMP018 Hemophilic Arthropathy 35 0.032
431
c LKM004 Leukemia, B-Cell, Chronic 35 0.032
432
NRV004 Nerve Compression Syndrome 35 0.032
433
c LKM005 Leukemia, T-Cell, Chronic 35 0.032
434
EPD005 Epidural Abscess 35 0.032
435
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.032
436
DSS010 Dissociative Disorder 35 0.032
437
BNN005 Bunion 34 0.032
438
FTD001 Foot Drop 34 0.032
439
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 34 0.032
440
PPL052 Papillomatosis, Confluent and Reticulated 34 0.032
441
CRD016 Cardiac Rupture 33 0.032
442
TTH007 Tooth Erosion 32 0.032
443
CYT004 Cytomegalic Inclusion Disease 32 0.032
444
ALR002 Al-Raqad Syndrome 32 0.032
445
c JVN024 Juvenile Hereditary Hemochromatosis 32 0.032
446
PLN007 Plantar Fasciitis 32 0.032
447
PYR016 Pyridoxine Deficiency 31 0.032
448
MYC088 Mycobacterium Avium Complex Infections 30 0.032
449
ULN001 Ulnar Neuropathy 30 0.032
450
P SKL032 Skeletal Muscle Disease 30 0.032
451
SPN392 Spondylosis, Cervical 29 0.032
452
PST092 Posttransplant Acute Limbic Encephalitis 29 0.032
453
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.032
454
P ACT232 Acute Necrotizing Encephalopathy 28 0.032
455
KDN013 Kidney Hypertrophy 27 0.032
456
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.032
457
EXT012 Extraskeletal Chondroma 25 0.032
458
CLC064 Calcifying Aponeurotic Fibroma 23 0.032
459
c GLC079 Glaucoma 1, Open Angle, P 23 0.032
460
LTR004 Lateral Myocardial Infarction 23 0.032
461
MSC148 Musical Perfect Pitch 22 0.032
462
VLK001 Volkmann Contracture 22 0.032
463
AND005 Androgen Insensitivity Syndrome, Mild 20 0.032
464
PRD026 Pre-Descemet Corneal Dystrophy 19 0.032
465
c CHR120 Charcot-Marie-Tooth Neuropathy X Type 1 19 0.032
466
BLD137 Blood Group--Ahonen 17 0.032
467
c SYS048 Systemic Lupus Erythematosus 8 16 0.032
468
WLF014 Wolfram Syndrome, Mitochondrial Form 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 15 0.032
471
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.032
472
CHL110 Childhood Encephalopathy Due to Thiamine Pyrophosphokinase Deficiency 12 0.032
473
NRL025 Neural Tube Closure Defect 12 0.032
474
DFN002 Dfnx1 Nonsyndromic Hearing Loss and Deafness 8 0.032
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