Search results for heme

862 hits were found for heme

# Family MCID Name MIFTS Score
1
HMX003 Heme Oxygenase 1 Deficiency 26 7.467
2
c PRT132 Protoporphyria, Erythropoietic, 1 59 4.672
3
P PRP029 Porphyria 58 3.113
4
IRN002 Iron Metabolism Disease 58 0.257
5
ISC004 Ischemia 62 0.247
6
HLX001 Helix Syndrome 46 0.241
7
DFC004 Deficiency Anemia 77 0.240
8
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.222
9
c ACT210 Acute Respiratory Distress Syndrome 59 0.213
10
ERY051 Erythroleukemia, Familial 58 0.210
11
BLR008 Bilirubin Metabolic Disorder 58 0.198
12
HYP266 Hypoxia 58 0.193
13
P VSC007 Vascular Disease 65 0.190
14
P SCK005 Sickle Cell Disease 53 0.188
15
P ALZ034 Alzheimer Disease 90 0.176
16
c PRC016 Pre-Eclampsia 63 0.175
17
HMS001 Hemosiderosis 54 0.175
18
ATH013 Atherosclerosis Susceptibility 68 0.173
19
P RRH023 Rare Hereditary Hemochromatosis 41 0.171
20
IRN001 Iron Deficiency Anemia 59 0.160
21
MLR004 Malaria 82 0.158
22
HMP009 Haemophilus Influenzae 46 0.158
23
PRP083 Porphyria, Acute Intermittent 62 0.156
24
P KDN018 Kidney Disease 73 0.152
25
P HML002 Hemolytic Anemia 64 0.152
26
P CLR023 Colorectal Cancer 100 0.150
27
P THL005 Thalassemia 62 0.146
28
c ACT071 Acute Kidney Failure 60 0.144
29
P SDR003 Sideroblastic Anemia 47 0.142
30
P PLM037 Pulmonary Hypertension 69 0.140
31
HYP066 Hyperglycemia 63 0.135
32
c ACT078 Acute Porphyria 49 0.135
33
P PRD008 Periodontitis 66 0.133
34
BRN071 Brain Injury 51 0.128
35
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.128
36
P LVR013 Liver Disease 71 0.119
37
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.119
38
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.119
39
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.116
40
LVR012 Liver Cirrhosis 67 0.116
41
P PRP003 Porphyria Cutanea Tarda 66 0.111
42
CHG001 Chagas Disease 66 0.111
43
P MYL006 Myeloid Leukemia 61 0.111
44
TRM010 Traumatic Brain Injury 54 0.111
45
P PRK057 Parkinson Disease, Late-Onset 77 0.108
46
CYT002 Cytokine Deficiency 46 0.108
47
P NRB010 Neuroblastoma 1 66 0.105
48
CLT003 Colitis 63 0.105
49
P INF037 Inflammatory Bowel Disease 57 0.105
50
ALL014 Allergic Encephalomyelitis 40 0.105
51
P PLM036 Pulmonary Fibrosis 66 0.102
52
IDP011 Idiopathic Interstitial Pneumonia 65 0.102
53
48X005 48,xyyy 37 0.102
54
ATM095 Autoimmune Disease 62 0.099
55
c ACT027 Acute Pancreatitis 60 0.099
56
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.099
57
BCT022 Bacterial Infectious Disease 57 0.099
58
PRP082 Porphyria, Congenital Erythropoietic 55 0.099
59
CRB004 Cerebral Artery Occlusion 38 0.099
60
CHL068 Cholestasis 61 0.096
61
PRT013 Portal Hypertension 61 0.096
62
VRG001 Variegate Porphyria 55 0.096
63
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.096
64
NNT012 Neonatal Jaundice 48 0.096
65
SCK003 Sickle Cell Anemia 74 0.092
66
P PHC003 Pheochromocytoma 71 0.092
67
c CHR684 Chronic Kidney Disease 68 0.092
68
TXC005 Toxic Shock Syndrome 63 0.092
69
SPN186 Spinal Cord Injury 63 0.092
70
FTT001 Fatty Liver Disease 63 0.092
71
c MCR113 Microvascular Complications of Diabetes 3 55 0.092
72
ADR040 Adrenal Gland Pheochromocytoma 51 0.092
73
c MCR120 Microvascular Complications of Diabetes 7 48 0.092
74
c MCR130 Microvascular Complications of Diabetes 6 42 0.092
75
c MCR133 Microvascular Complications of Diabetes 4 42 0.092
76
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.089
77
P CRN018 Coronary Artery Anomaly 67 0.089
78
P GLM045 Glioma 64 0.089
79
HMG005 Hemoglobinopathy 57 0.089
80
BRN004 Brain Edema 57 0.089
81
GLL048 Glial Tumor 48 0.089
82
P LNG032 Lung Cancer 99 0.086
83
c HPT073 Hepatitis C Virus 74 0.086
84
c HMC039 Hemochromatosis, Type 1 73 0.086
85
ART140 Arteries, Anomalies of 60 0.086
86
P CRN300 Coronary Heart Disease 1 59 0.086
87
ANT024 Anthrax Disease 56 0.086
88
c ACT134 Acute Liver Failure 53 0.086
89
BNR002 Bone Resorption Disease 51 0.086
91
P GST053 Gastric Cancer 85 0.082
92
P LNG064 Lung Cancer Susceptibility 3 79 0.082
93
GLB002 Glioblastoma 74 0.082
94
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.082
95
c BTT014 Beta-Thalassemia 73 0.082
96
P LKM002 Leukemia 69 0.082
97
PRT037 Pertussis 66 0.082
98
LNG099 Lung Disease 62 0.082
99
c HPT001 Hepatitis C 62 0.082
100
GLB015 Glioblastoma Multiforme 60 0.082
101
c PRD040 Periodontitis, Chronic 56 0.082
102
LMB062 Limb Ischemia 50 0.082
103
ANX004 Anoxia 44 0.082
104
MYL009 Myelodysplastic Syndrome 72 0.078
105
PRT036 Peritonitis 66 0.078
106
LSH001 Leishmaniasis 64 0.078
107
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.078
108
CPR004 Coproporphyria, Hereditary 57 0.078
109
PLM010 Pulmonary Edema 56 0.078
110
NTR046 Neutrophil Migration 49 0.078
111
RNL077 Renal Fibrosis 49 0.078
112
P KLZ004 Kala-Azar 1 43 0.078
113
P BRS047 Breast Cancer 99 0.074
114
P PNC035 Pancreatic Cancer 86 0.074
115
c HYP836 Hypercholesterolemia, Familial, 1 74 0.074
116
CRB039 Cerebrovascular Disease 71 0.074
117
P VSC011 Vasculitis 64 0.074
118
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.074
119
ORL011 Oral Cancer 62 0.074
120
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.074
121
P GLM007 Glomerulonephritis 58 0.074
122
P NRP001 Neuropathy 57 0.074
123
P ECL001 Eclampsia 53 0.074
124
NNL006 Non-Alcoholic Steatohepatitis 53 0.074
125
RTN003 Retinal Ischemia 52 0.074
126
CTN011 Cutaneous Porphyria 36 0.074
127
PPL052 Papillomatosis, Confluent and Reticulated 34 0.074
128
ESP021 Esophageal Cancer 90 0.070
129
c LKM061 Leukemia, Acute Myeloid 84 0.070
130
P BLD134 Bladder Cancer 79 0.070
131
SVR004 Severe Combined Immunodeficiency 74 0.070
132
OTT002 Otitis Media 71 0.070
133
P DMN001 Diamond-Blackfan Anemia 69 0.070
134
P DRM053 Dermatitis, Atopic 68 0.070
135
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.070
136
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.070
137
P PSR002 Psoriasis 63 0.070
138
SQM006 Squamous Cell Carcinoma 60 0.070
139
END030 End Stage Renal Failure 60 0.070
140
P RHN004 Rhinitis 59 0.070
141
c ACT075 Acute Myocardial Infarction 59 0.070
142
AGN016 Aging 58 0.070
143
ALL006 Allergic Asthma 56 0.070
144
GST037 Gastroparesis 52 0.070
145
c INH020 Inherited Metabolic Disorder 51 0.070
146
HMG002 Hemoglobinuria 49 0.070
147
ORL015 Oral Squamous Cell Carcinoma 44 0.070
148
c HYP595 Hypertension, Essential 87 0.065
149
P HRT032 Heart Disease 78 0.065
150
ULC004 Ulcerative Colitis 75 0.065
151
P GRF003 Graft-Versus-Host Disease 71 0.065
152
ART016 Aortic Aneurysm 71 0.065
153
LGH007 Leigh Syndrome 69 0.065
154
CNG034 Congestive Heart Failure 69 0.065
155
ALL003 Allergic Rhinitis 69 0.065
156
P HYP098 Hypereosinophilic Syndrome 67 0.065
157
P DBT009 Diabetes Mellitus 66 0.065
158
P ADN016 Adenocarcinoma 65 0.065
159
ALL026 Allergic Hypersensitivity Disease 65 0.065
160
P BCL017 B-Cell Lymphoma 61 0.065
161
DPH001 Diphtheria 61 0.065
162
THR024 Thrombosis 58 0.065
163
P DNG005 Dengue Virus 57 0.065
164
P ART021 Arteriosclerosis 56 0.065
165
P HMC002 Homocystinuria 52 0.065
166
PST011 Pustulosis of Palm and Sole 51 0.065
167
URM002 Uremia 50 0.065
168
URT010 Ureteral Obstruction 46 0.065
169
MCR018 Microcytic Anemia 46 0.065
170
HYP001 Hypochromic Microcytic Anemia 38 0.065
171
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 24 0.065
172
P HRM022 Hair Morphology 1 15 0.065
173
STR067 Stroke, Ischemic 82 0.061
174
KPS004 Kaposi Sarcoma 75 0.061
175
P MYC007 Myocardial Infarction 74 0.061
176
P SLP006 Sleep Apnea 71 0.061
177
P MCR115 Microvascular Complications of Diabetes 5 67 0.061
178
c SML038 Small Cell Cancer of the Lung 67 0.061
179
SKN016 Skin Disease 64 0.061
180
P PNC044 Pancreatitis 61 0.061
181
ANR040 Aneurysm 60 0.061
182
c VRL010 Viral Hepatitis 56 0.061
183
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.061
184
HMT018 Hematopoietic Stem Cell Transplantation 54 0.061
185
P HML001 Hemolytic-Uremic Syndrome 54 0.061
186
IMP005 Impotence 53 0.061
187
PRP080 Peripheral Artery Disease 51 0.061
188
P RNV001 Renovascular Hypertension 49 0.061
189
RDC006 Red Cell Aplasia 45 0.061
190
P HPT023 Hepatocellular Carcinoma 99 0.055
191
IMM167 Immune Deficiency Disease 79 0.055
192
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.055
193
c ATR087 Atrial Standstill 1 76 0.055
194
P RSP003 Respiratory Failure 75 0.055
195
PRP027 Peripheral Vascular Disease 72 0.055
196
P HNT016 Huntington Disease 72 0.055
197
P PNM007 Pneumonia 71 0.055
198
P THR014 Thrombocytopenia 67 0.055
199
ANG054 Angina Pectoris 66 0.055
200
LPD008 Lipid Metabolism Disorder 64 0.055
201
P NTR004 Neutropenia 64 0.055
202
P END044 Endometriosis 63 0.055
203
TRN015 Transient Cerebral Ischemia 62 0.055
204
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.055
205
BRN002 Bronchiolitis 60 0.055
206
P SZR006 Seizure Disorder 59 0.055
207
VSL002 Visual Epilepsy 58 0.055
208
GST033 Gestational Diabetes 58 0.055
209
BRN056 Bronchopulmonary Dysplasia 57 0.055
210
P PLY018 Polycythemia 56 0.055
211
DBT010 Diabetic Neuropathy 56 0.055
212
BRN012 Bronchiolitis Obliterans 55 0.055
213
HYP060 Hyperinsulinism 55 0.055
214
GLC003 Glucose Intolerance 55 0.055
215
P TYR004 Tyrosinemia 54 0.055
216
c ACT135 Acute Graft Versus Host Disease 52 0.055
217
ENT011 Enterocolitis 51 0.055
218
SPL018 Splenomegaly 48 0.055
219
P KRN004 Kernicterus 47 0.055
220
SLP001 Sleeping Sickness 47 0.055
221
CHR074 Choriocarcinoma 47 0.055
222
P PRR002 Pure Red-Cell Aplasia 47 0.055
223
DYS015 Dysentery 45 0.055
224
ACT003 Acute Kidney Tubular Necrosis 42 0.055
225
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.055
226
HMG010 Hemoglobinemia 29 0.055
227
P PRS040 Prostate Cancer 97 0.049
228
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.049
230
MYL069 Myeloma, Multiple 85 0.049
231
P ATX030 Ataxia-Telangiectasia 83 0.049
232
INS024 Insulin-Like Growth Factor I 79 0.049
233
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.049
234
CRV035 Cervical Cancer 77 0.049
235
P MLT020 Multiple Sclerosis 73 0.049
236
P CRD119 Cardiac Arrest 71 0.049
237
P HYP061 Hypertrophic Cardiomyopathy 68 0.049
238
P MSC005 Muscular Dystrophy 68 0.049
239
P NPH012 Nephrotic Syndrome 65 0.049
240
KWS002 Kawasaki Disease 65 0.049
241
CLN015 Colon Adenocarcinoma 65 0.049
242
P PRP019 Peripheral Nervous System Disease 64 0.049
243
P ENC018 Encephalopathy 64 0.049
244
DRM006 Dermatitis 63 0.049
245
MCR013 Microphthalmia 62 0.049
246
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.049
247
PPT005 Peptic Ulcer Disease 60 0.049
248
P MYC008 Myocarditis 60 0.049
249
P KDN017 Kidney Cancer 60 0.049
250
ADN018 Adenoma 60 0.049
251
c ACT073 Acute Leukemia 59 0.049
252
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.049
253
DSS009 Disseminated Intravascular Coagulation 58 0.049
254
c ANM036 Anemia, Sideroblastic, 1 56 0.049
255
PRP030 Purpura 56 0.049
256
P LYM031 Lymphocytic Leukemia 56 0.049
257
P LTR001 Lateral Sclerosis 56 0.049
258
P PLM034 Pulmonary Emphysema 55 0.049
259
MTC097 Mitochondrial Complex Iv Deficiency 55 0.049
260
VSC003 Visceral Leishmaniasis 55 0.049
261
HMC014 Homocysteinemia 54 0.049
262
PLS007 Plasmodium Falciparum Malaria 53 0.049
263
TLN003 Telangiectasis 53 0.049
264
P AST007 Astrocytoma 52 0.049
265
PLC008 Placenta Disease 51 0.049
266
ILS001 Ileus 51 0.049
267
THR016 Thrombophlebitis 50 0.049
268
P OBS001 Obstructive Jaundice 49 0.049
269
LYM019 Lymphosarcoma 48 0.049
270
P CLL015 Collagen Disease 46 0.049
271
PST092 Posttransplant Acute Limbic Encephalitis 29 0.049
272
c SYS001 Systemic Lupus Erythematosus 88 0.043
273
CYS001 Cystic Fibrosis 84 0.043
274
NRL016 Neural Tube Defects 83 0.043
275
AST005 Asthma 80 0.043
276
OST012 Osteoarthritis 80 0.043
277
P RTN024 Retinoblastoma 74 0.043
278
c LKM063 Leukemia, Chronic Myeloid 74 0.043
279
c SPN225 Spondyloarthropathy 1 74 0.043
280
HMN044 Human Immunodeficiency Virus Type 1 73 0.043
281
MSC157 Muscular Dystrophy, Duchenne Type 70 0.043
282
P LYM118 Lymphoma 70 0.043
283
P INF038 Influenza 69 0.043
284
P HPT021 Hepatitis 69 0.043
285
CHL065 Cholangiocarcinoma 68 0.043
286
c HML033 Hemolytic Uremic Syndrome, Atypical 1 67 0.043
287
P OLG002 Oligodendroglioma 67 0.043
288
P SKN015 Skin Carcinoma 67 0.043
289
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.043
290
P ENC004 Encephalitis 64 0.043
291
c HPT016 Hepatitis B 63 0.043
292
P RHB003 Rhabdomyosarcoma 62 0.043
293
VRL011 Viral Infectious Disease 62 0.043
294
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.043
295
c SCL052 Scleroderma, Familial Progressive 62 0.043
296
c DNG003 Dengue Disease 61 0.043
297
ACQ007 Acquired Immunodeficiency Syndrome 61 0.043
298
P ADL010 Adult Respiratory Distress Syndrome 61 0.043
299
c ANM038 Anemia, Autoimmune Hemolytic 61 0.043
300
PLM033 Pulmonary Embolism 60 0.043
301
HPT019 Hepatic Encephalopathy 60 0.043
302
P BRS044 Breast Adenocarcinoma 59 0.043
303
P UVT001 Uveitis 58 0.043
304
P ALP008 Alopecia 58 0.043
305
P EXN002 Exanthem 58 0.043
306
YLL002 Yellow Fever 58 0.043
307
GLB001 Gilbert Syndrome 58 0.043
308
INT007 Intermediate Coronary Syndrome 58 0.043
309
P GST044 Gastritis 58 0.043
310
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.043
311
SCH014 Schistosomiasis 57 0.043
312
GST050 Gastrointestinal System Disease 57 0.043
313
RHM027 Rheumatic Disease 56 0.043
314
FLR002 Filariasis 56 0.043
315
SLC006 Silicosis 55 0.043
316
P HYP076 Hyperthyroidism 55 0.043
317
PRN019 Perinatal Necrotizing Enterocolitis 55 0.043
318
PRS045 Prostatic Hypertrophy 55 0.043
319
INT079 Intrahepatic Cholangiocarcinoma 54 0.043
320
P RCT021 Rectum Cancer 54 0.043
321
OCL069 Ocular Motor Apraxia 53 0.043
322
P MNC007 Monocytic Leukemia 52 0.043
323
THR004 Thrombocytosis 52 0.043
324
PRS021 Prostatic Adenoma 52 0.043
325
GSG001 Gas Gangrene 52 0.043
326
P CHR345 Chronic Pain 52 0.043
327
AZS001 Azoospermia 51 0.043
328
CRY005 Cryptococcosis 51 0.043
329
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.043
330
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.043
331
FLR001 Filarial Elephantiasis 51 0.043
332
c SVR005 Severe Pre-Eclampsia 50 0.043
333
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.043
334
TRY001 Trypanosomiasis 50 0.043
335
PRS129 Prostatic Hyperplasia, Benign 49 0.043
336
HPT009 Hepatopulmonary Syndrome 49 0.043
337
47X002 47,xyy 49 0.043
338
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.043
339
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.043
340
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.043
341
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.043
342
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.043
343
P BNG032 Benign Mesothelioma 47 0.043
344
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.043
345
c FML008 Familial Retinoblastoma 46 0.043
346
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.043
347
ENT004 Enthesopathy 46 0.043
348
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.043
349
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.043
350
c ATS307 Autosomal Recessive Cerebellar Ataxia 44 0.043
351
c PCH010 Pachyonychia Congenita 3 43 0.043
352
c HMG003 Hemoglobin E Disease 43 0.043
353
SBC016 Subacute Delirium 43 0.043
354
P SDR002 Siderosis 42 0.043
355
HPT004 Hepatic Coma 42 0.043
356
GST020 Gastric Antral Vascular Ectasia 42 0.043
357
MCR017 Macrocytic Anemia 41 0.043
358
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.043
359
WLL004 Wallerian Degeneration 40 0.043
360
PST036 Posterior Column Ataxia with Retinitis Pigmentosa 39 0.043
361
PRT094 Protoporphyria, Erythropoietic, X-Linked 33 0.043
362
MCL057 Macular Dystrophy with Central Cone Involvement 32 0.043
363
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.043
364
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.043
365
PRQ002 Paraquat Poisoning 25 0.043
366
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.043
367
MTC150 Mitochondrial Complex V Deficiency, Mitochondrial Type 1 24 0.043
368
PST040 Posterior Column Ataxia 22 0.043
369
c HRM021 Hair Morphology 2 20 0.043
370
c PRT135 Protoporphyria, Erythropoietic, 2 18 0.043
371
HYP171 Hyperphenylalaninemia Due to Dehydratase Deficiency 16 0.043
372
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.035
373
P OVR042 Ovarian Cancer 89 0.035
374
P RHM011 Rheumatoid Arthritis 82 0.035
375
c DLT002 Dilated Cardiomyopathy 81 0.035
376
P MDL005 Medulloblastoma 78 0.035
377
P RTN008 Retinitis Pigmentosa 77 0.035
378
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.035
379
CRH001 Crohn's Disease 75 0.035
380
c THR092 Thrombophilia Due to Thrombin Defect 74 0.035
381
P FML011 Familial Adenomatous Polyposis 73 0.035
382
P CNR004 Cone-Rod Dystrophy 2 72 0.035
383
PLM001 Pulmonary Tuberculosis 72 0.035
384
LPT014 Leptin Deficiency or Dysfunction 72 0.035
385
P AMY004 Amyloidosis 71 0.035
386
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.035
387
P CHR012 Chronic Granulomatous Disease 69 0.035
388
P HYD006 Hydrocephalus 68 0.035
389
HYP056 Hypoglycemia 68 0.035
390
CNN005 Connective Tissue Disease 68 0.035
391
P LKM062 Leukemia, Acute Lymphoblastic 68 0.035
392
MLN008 Melanoma 68 0.035
393
c JVN010 Juvenile Rheumatoid Arthritis 67 0.035
394
SRC014 Sarcoma 67 0.035
395
OST159 Osteogenic Sarcoma 67 0.035
396
P BLD062 Bile Duct Cancer 66 0.035
397
P TRN020 Turner Syndrome 66 0.035
398
P HRS035 Hirschsprung Disease 1 65 0.035
399
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.035
400
c RHB024 Rhabdomyosarcoma 2 64 0.035
401
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.035
402
ART002 Arts Syndrome 63 0.035
403
c ACT068 Acute Cystitis 63 0.035
404
GT001 Gout 63 0.035
405
c ALP101 Alpha-Thalassemia 63 0.035
406
P MYP004 Myopathy 63 0.035
407
P FCL005 Focal Segmental Glomerulosclerosis 63 0.035
408
P ESP024 Esophagitis 62 0.035
409
BRC012 Brucellosis 62 0.035
410
THY029 Thyroid Carcinoma 62 0.035
411
P CTR002 Cataract 62 0.035
412
DGR001 Digeorge Syndrome 61 0.035
413
P ALP009 Alopecia Areata 61 0.035
414
P CRG003 Crigler-Najjar Syndrome, Type I 61 0.035
415
P ART023 Arthropathy 61 0.035
416
CTN007 Cutaneous Leishmaniasis 61 0.035
417
NTR005 Nutritional Deficiency Disease 61 0.035
418
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.035
419
c TYR012 Tyrosinemia, Type I 61 0.035
420
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.035
421
SPP011 Suppression of Tumorigenicity 12 61 0.035
422
CHL123 Chlamydia 60 0.035
423
ALC006 Alcoholic Hepatitis 60 0.035
424
GST045 Gastroenteritis 60 0.035
425
P INF032 Infertility 60 0.035
426
EYD002 Eye Disease 59 0.035
427
DNG002 Dengue Hemorrhagic Fever 59 0.035
428
CNS004 Constipation 59 0.035
429
P MTR012 Mitral Valve Disease 59 0.035
430
HYD002 Hydronephrosis 58 0.035
431
CNT047 Contact Dermatitis 58 0.035
432
CHL014 Cholera 58 0.035
433
HPT022 Hepatoblastoma 58 0.035
434
CMM005 Common Cold 57 0.035
435
P PLY041 Polymyositis 57 0.035
436
P FBR017 Fibrosarcoma 57 0.035
437
VSC002 Vascular Dementia 57 0.035
438
SPN035 Spindle Cell Sarcoma 57 0.035
439
ENH001 Enhanced S-Cone Syndrome 56 0.035
440
PHR003 Pharyngitis 56 0.035
441
DFF005 Diffuse Large B-Cell Lymphoma 56 0.035
442
PPL022 Papilloma 56 0.035
443
SNS003 Sensory Peripheral Neuropathy 56 0.035
444
c CNG216 Congenital Hydrocephalus 55 0.035
445
SYN007 Synovitis 55 0.035
446
MST005 Mastitis 55 0.035
447
HYP005 Hypokalemia 55 0.035
448
P DRR001 Diarrhea 55 0.035
449
PLC005 Placental Insufficiency 55 0.035
450
ORL004 Oral Submucous Fibrosis 55 0.035
451
P FBR031 Febrile Seizures 54 0.035
452
PLG002 Plague 54 0.035
453
P MMB011 Membranous Nephropathy 54 0.035
454
CLR030 Clear Cell Renal Cell Carcinoma 54 0.035
455
P RTN018 Retinal Disease 53 0.035
456
SPN051 Spondylitis 53 0.035
457
c GLL024 Gallbladder Disease 1 53 0.035
458
RGH009 Right Atrial Isomerism 52 0.035
459
P THR015 Thrombophilia 51 0.035
460
PRN011 Pernicious Anemia 51 0.035
461
CLR109 Colorectal Adenocarcinoma 51 0.035
462
c OPT053 Optic Atrophy 1 51 0.035
463
IMM064 Immunodeficiency, Common Variable, 10 51 0.035
464
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 50 0.035
465
ONC002 Onchocerciasis 50 0.035
466
MTC005 Mitochondrial Metabolism Disease 50 0.035
467
IGG001 Iga Glomerulonephritis 50 0.035
468
RFR010 Refractory Anemia 50 0.035
469
TST044 Testicular Torsion 49 0.035
470
DGN001 Degenerative Disc Disease 49 0.035
471
SQM002 Squamous Cell Papilloma 49 0.035
472
ATS010 Autosomal Recessive Disease 49 0.035
473
SPT005 Spotted Fever 48 0.035
474
P TCL004 T-Cell Leukemia 48 0.035
475
ATN005 Autonomic Dysfunction 48 0.035
476
PLM035 Pulmonary Eosinophilia 47 0.035
477
ACT017 Acute Chest Syndrome 47 0.035
478
P MTH007 Methemoglobinemia 47 0.035
479
PRP007 Priapism 47 0.035
480
RTN023 Retinitis 46 0.035
481
P PRP056 Porphyria, Acute Hepatic 46 0.035
482
NRR001 Neuroretinitis 46 0.035
483
c MLG068 Malignant Glioma 46 0.035
484
MYC005 Myocardial Stunning 45 0.035
485
OBS082 Obstructive Nephropathy 44 0.035
486
INT052 Intestinal Volvulus 44 0.035
487
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.035
488
PRL023 Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome 42 0.035
489
CRB086 Cerebral Aneurysms 41 0.035
490
PRM329 Premature Aging 41 0.035
491
CLN044 Colon Adenoma 41 0.035
492
THR123 Thrombotic Microangiopathy 41 0.035
493
RCK002 Rocky Mountain Spotted Fever 40 0.035
494
CRN020 Coronary Restenosis 40 0.035
495
SPR066 Superficial Siderosis 38 0.035
496
BTN004 Biotin Deficiency 38 0.035
497
AML001 Amelanotic Melanoma 38 0.035
498
FTL004 Fetal Erythroblastosis 38 0.035
499
CHN002 Chancroid 36 0.035
500
FST010 Fasting Hypoglycemia 36 0.035
501
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 36 0.035
502
OLV004 Oliver-Mcfarlane Syndrome 36 0.035
503
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.035
504
c LKM005 Leukemia, T-Cell, Chronic 35 0.035
505
INF009 Inflammatory Spondylopathy 29 0.035
506
CHL079 Children's Interstitial Lung Disease 27 0.035
507
c ATS210 Autosomal Recessive Sideroblastic Anemia 27 0.035
508
TRY004 Trypanosomiasis, Human East-African 25 0.035
509
ANT078 Antipyrine Metabolism 24 0.035
510
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.035
511
LWF001 Low-Flow Priapism 19 0.035
512
XLN067 X-Linked Protoporphyria 15 0.035
513
c LKM071 Leukemia, Chronic Lymphocytic 81 0.025
514
c FNC027 Fanconi Anemia, Complementation Group a 81 0.025
515
GST019 Gastrointestinal Stromal Tumor 76 0.025
516
P APL001 Aplastic Anemia 76 0.025
517
END057 Endometrial Cancer 74 0.025
518
c MNN043 Meningioma, Familial 74 0.025
519
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.025
520
AGM019 Agammaglobulinemia, X-Linked 71 0.025
521
PLY001 Polycythemia Vera 70 0.025
522
BRN024 Bronchitis 70 0.025
523
P HYP086 Hypothyroidism 70 0.025
524
FRN006 Frontotemporal Dementia 70 0.025
525
LYM133 Lymphoma, Hodgkin, Classic 70 0.025
526
c PNC108 Pancreatitis, Hereditary 70 0.025
527
c WLM013 Wilms Tumor 1 69 0.025
528
c HMP029 Hemophilia a 69 0.025
529
P SYS005 Systemic Scleroderma 68 0.025
530
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.025
531
SKN019 Skin Melanoma 68 0.025
532
P NRV007 Nervous System Disease 68 0.025
533
c BSL007 Basal Cell Carcinoma 68 0.025
534
P NSP012 Nasopharyngeal Carcinoma 67 0.025
535
P ATR011 Atrial Fibrillation 67 0.025
536
c MCR129 Microvascular Complications of Diabetes 1 67 0.025
537
c ART101 Aortic Valve Disease 2 67 0.025
538
GST040 Gastric Adenocarcinoma 67 0.025
539
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.025
540
P AGM001 Agammaglobulinemia 66 0.025
541
c DPH024 Diaphragmatic Hernia, Congenital 66 0.025
542
MLD001 Melioidosis 66 0.025
543
P HRP006 Herpes Simplex 66 0.025
544
LNG039 Lung Squamous Cell Carcinoma 66 0.025
545
P MTR014 Motor Neuron Disease 66 0.025
546
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.025
547
P ANG001 Angelman Syndrome 65 0.025
548
OST017 Osteomyelitis 65 0.025
549
MSC007 Muscle Hypertrophy 65 0.025
550
P FRD012 Friedreich Ataxia 1 65 0.025
551
P CHR071 Charcot-Marie-Tooth Disease 65 0.025
552
IRR002 Irritable Bowel Syndrome 65 0.025
553
TBC004 Tobacco Addiction 65 0.025
554
CLR108 Colorectal Adenoma 64 0.025
555
ANR007 Anorexia Nervosa 64 0.025
556
LYM017 Lyme Disease 64 0.025
557
P HYP069 Hyperparathyroidism 64 0.025
558
P THY023 Thymoma 64 0.025
559
MNN042 Meningioma, Radiation-Induced 64 0.025
560
HMT002 Hematologic Cancer 64 0.025
561
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.025
562
APN008 Apnea, Obstructive Sleep 64 0.025
563
P ANR048 Aniridia 1 64 0.025
564
ACT119 Acute Promyelocytic Leukemia 63 0.025
565
c WLM018 Wilms Tumor 5 63 0.025
566
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 62 0.025
567
ADL002 Adult Syndrome 62 0.025
568
c BRN108 Branchiootic Syndrome 1 62 0.025
569
P HMN010 Hemangioma 62 0.025
570
OST003 Osteonecrosis 62 0.025
571
P HYP750 Hypertriglyceridemia, Familial 62 0.025
572
NRM005 Neuromuscular Disease 62 0.025
573
GTL001 Gitelman Syndrome 62 0.025
574
P ART067 Aortic Aneurysm, Familial Thoracic 1 62 0.025
575
RTN017 Retinal Detachment 62 0.025
576
ACN002 Acanthosis Nigricans 62 0.025
577
c HYD046 Hydatidiform Mole, Recurrent, 1 62 0.025
578
LKD001 Leukodystrophy 61 0.025
579
STT001 Status Epilepticus 61 0.025
580
c LCL006 Localized Scleroderma 61 0.025
582
P TXP001 Toxoplasmosis 61 0.025
583
P PLY014 Polycystic Kidney Disease 61 0.025
584
VRC005 Varicose Veins 61 0.025
585
IGR001 Ige Responsiveness, Atopic 61 0.025
586
HLC007 Helicobacter Pylori Infection 61 0.025
587
P CND004 Candidiasis 61 0.025
588
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.025
589
GNG013 Gingivitis 60 0.025
590
PNM010 Pneumothorax, Primary Spontaneous 60 0.025
591
BND020 Bone Disease 60 0.025
592
c PRM005 Primary Hyperparathyroidism 60 0.025
593
c ADL017 Adult T-Cell Leukemia 59 0.025
594
HMR039 Hemorrhage, Intracerebral 59 0.025
595
P CYS018 Cystitis 59 0.025
596
SZR001 Sezary's Disease 59 0.025
597
P BPL003 Bipolar Disorder 59 0.025
598
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.025
599
ADL030 Adult-Onset Still's Disease 59 0.025
600
c MST023 Mesothelioma, Malignant 59 0.025
601
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.025
602
P END033 Endocarditis 58 0.025
603
P PLY011 Polycystic Ovary Syndrome 58 0.025
604
EXT034 Extrinsic Allergic Alveolitis 58 0.025
605
CYT008 Cytomegalovirus Infection 58 0.025
606
c ESS001 Essential Tremor 58 0.025
607
P HMP007 Hemophilia 58 0.025
608
BRG013 Buerger Disease 58 0.025
609
LYM027 Lymphopenia 58 0.025
610
PYR041 Pyruvate Kinase Deficiency of Red Cells 58 0.025
611
P PYL005 Pyelonephritis 58 0.025
612
P SLP005 Sleep Disorder 58 0.025
613
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.025
614
P TRC086 Trichohepatoenteric Syndrome 1 57 0.025
615
ALK013 Alkaptonuria 57 0.025
616
TNG003 Tongue Cancer 57 0.025
617
P MTC069 Mitochondrial Disorders 57 0.025
618
PRM236 Primary Biliary Cholangitis 57 0.025
619
P MLN007 Male Infertility 57 0.025
620
INT030 Intracranial Aneurysm 57 0.025
621
ACT200 Acute Monoblastic Leukemia 56 0.025
622
ALL010 Allergic Contact Dermatitis 56 0.025
623
P BNC003 Bone Cancer 56 0.025
624
PNM008 Pneumothorax 56 0.025
625
P RTN016 Retinal Degeneration 56 0.025
626
c CNT035 Central Nervous System Disease 56 0.025
627
HNC001 Henoch-Schoenlein Purpura 56 0.025
628
JPN002 Japanese Encephalitis 56 0.025
629
P HYP024 Hypoparathyroidism 56 0.025
630
P INT068 Intestinal Disease 56 0.025
631
AVN001 Avian Influenza 56 0.025
632
GRN051 Granulomatous Disease, Chronic, X-Linked 55 0.025
633
AMN003 Amnestic Disorder 55 0.025
634
c THY107 Thymoma, Familial 55 0.025
635
P CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.025
636
ADN027 Adenomyosis 55 0.025
637
P TRM003 Tremor 55 0.025
638
P PLY019 Polyneuropathy 55 0.025
639
LST001 Listeriosis 55 0.025
640
MXD005 Mixed Connective Tissue Disease 55 0.025
641
SPT004 Septic Arthritis 55 0.025
642
c LKM070 Leukemia, Acute Monocytic 55 0.025
643
PST046 Post-Transplant Lymphoproliferative Disease 55 0.025
644
P INS002 in Situ Carcinoma 55 0.025
645
THY124 Thyroid Gland Papillary Carcinoma 54 0.025
646
P PRM006 Primary Biliary Cirrhosis 54 0.025
647
FCT001 Factor Viii Deficiency 54 0.025
648
GTR002 Goiter 54 0.025
649
P RST001 Restless Legs Syndrome 54 0.025
650
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.025
651
PNC001 Pancytopenia 54 0.025
652
TXC002 Toxic Encephalopathy 54 0.025
653
P MTR003 Mitral Valve Stenosis 54 0.025
654
SPP010 Suppressor of Tumorigenicity 3 54 0.025
655
P SLM003 Salmonellosis 54 0.025
656
INF034 Infective Endocarditis 53 0.025
657
EXP004 Exophthalmos 53 0.025
658
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.025
659
TCK001 Tick-Borne Encephalitis 53 0.025
660
HLL004 Hellp Syndrome 53 0.025
661
P TMP001 Temporal Lobe Epilepsy 53 0.025
662
CRT016 Carotid Artery Disease 53 0.025
663
ALC009 Alcoholic Liver Cirrhosis 53 0.025
664
MCP006 Mucoepidermoid Carcinoma 53 0.025
665
c PST005 Posterior Uveitis 52 0.025
666
OCL006 Ocular Hypertension 52 0.025
667
PNG002 Pain Agnosia 52 0.025
668
P CTN015 Cutaneous T Cell Lymphoma 52 0.025
669
P LCT001 Lactic Acidosis 52 0.025
670
NRT004 Neuritis 52 0.025
671
P TRT010 Teratoma 52 0.025
672
P MSC003 Muscular Atrophy 52 0.025
673
c CHR418 Chronic Leukemia 52 0.025
674
DYS014 Dyspepsia 51 0.025
675
c MLG054 Malignant Histiocytosis 51 0.025
676
VRC001 Varicocele 51 0.025
677
PNC034 Pancreas Disease 51 0.025
679
CHR005 Chorioamnionitis 51 0.025
680
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 51 0.025
681
P KRT007 Keratoconus 51 0.025
682
SLD003 Sialadenitis 51 0.025
683
P IGN003 Iga Nephropathy 1 50 0.025
684
VCC001 Vaccinia 50 0.025
685
c PNC106 Pancreatic Agenesis 1 50 0.025
686
c THR071 Thrombocytopenia 1 50 0.025
687
c AMY009 Amyloidosis Aa 50 0.025
688
P OVR046 Ovarian Cyst 50 0.025
689
P INT099 Intrahepatic Cholestasis of Pregnancy 50 0.025
690
MNN009 Meningoencephalitis 50 0.025
691
c HNT010 Huntington Disease-Like 1 49 0.025
692
CRN030 Coronary Stenosis 49 0.025
693
ESP002 Esophageal Varix 49 0.025
694
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.025
695
OPD006 Opioid Addiction 49 0.025
696
CVR006 Cavernous Hemangioma 49 0.025
697
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.025
698
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 49 0.025
699
THR013 Thoracic Outlet Syndrome 49 0.025
700
TST015 Testicular Disease 49 0.025
701
HPT014 Hepatorenal Syndrome 49 0.025
702
P PLG001 Pelger-Huet Anomaly 49 0.025
703
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.025
704
HYP781 Hypoascorbemia 48 0.025
705
INT051 Intussusception 48 0.025
706
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 48 0.025
707
SBP001 Subependymal Giant Cell Astrocytoma 48 0.025
708
P FNC004 Fanconi Syndrome 48 0.025
709
ACT098 Acute Erythroid Leukemia 48 0.025
710
OVR063 Overnutrition 47 0.025
711
PHS021 Phosphoglycerate Dehydrogenase Deficiency 47 0.025
712
P HMR005 Hemorrhoid 47 0.025
713
P MRC003 Mercury Poisoning 47 0.025
714
PYL006 Pyloric Stenosis 47 0.025
715
TTH006 Tooth Disease 47 0.025
716
CTS002 Cat-Scratch Disease 47 0.025
717
PPT001 Peptic Esophagitis 47 0.025
718
BBS001 Babesiosis 47 0.025
719
c MLG069 Malignant Hypertension 46 0.025
720
ZKF001 Zika Fever 46 0.025
721
TRC003 Trichomoniasis 46 0.025
722
GST010 Gestational Trophoblastic Neoplasm 46 0.025
723
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.025
724
RBF001 Riboflavin Deficiency 46 0.025
725
IRN004 Iron-Refractory Iron Deficiency Anemia 45 0.025
726
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.025
727
c PRM038 Primary Agammaglobulinemia 45 0.025
728
CRB090 Cerebral Hypoxia 45 0.025
729
c LRG001 Large Cell Carcinoma 45 0.025
730
CYN002 Cyanosis, Transient Neonatal 45 0.025
731
KHN001 Kuhnt-Junius Degeneration 45 0.025
732
TLR001 Tularemia 44 0.025
733
RTR008 Root Resorption 44 0.025
734
TCL003 T Cell Deficiency 44 0.025
735
PLR007 Pleural Empyema 44 0.025
736
PRM003 Premature Ejaculation 44 0.025
737
RFR003 Refractive Error 44 0.025
738
CRT015 Carotid Artery Occlusion 44 0.025
739
LSS003 Lassa Fever 44 0.025
740
OLG001 Oligospermia 44 0.025
741
PNN005 Panencephalitis, Subacute Sclerosing 43 0.025
742
ISC015 Ischemic Colitis 43 0.025
743
c CHR546 Chronic Mountain Sickness 43 0.025
744
c HMG001 Hemoglobin C Disease 43 0.025
745
DNG001 Dengue Shock Syndrome 43 0.025
746
SYS003 Systolic Heart Failure 43 0.025
747
ART006 Arthus Reaction 43 0.025
748
P MYG005 Myoglobinuria 43 0.025
749
MYC013 Mycobacterium Abscessus 42 0.025
750
VLV010 Vulvovaginitis 42 0.025
751
c MJR024 Major Affective Disorder 9 42 0.025
752
P GLM044 Glomerular Disease 42 0.025
753
c MCR112 Microvascular Complications of Diabetes 2 42 0.025
754
P HYP009 Hypertrophic Pyloric Stenosis 42 0.025
755
PCH007 Pouchitis 41 0.025
756
INT060 Intestinal Atresia 41 0.025
757
P BRB001 Beriberi 41 0.025
758
c TRC022 Tricuspid Valve Insufficiency 41 0.025
759
PLY100 Polyploidy 41 0.025
760
LKP003 Leukoplakia 40 0.025
761
MST004 Mast Cell Neoplasm 40 0.025
762
TRN004 Trench Fever 40 0.025
763
BBN001 Bubonic Plague 40 0.025
765
HST016 Histiocytic Sarcoma 40 0.025
766
SPN021 Spinal Meningioma 40 0.025
767
c FML015 Familial Nephrotic Syndrome 40 0.025
768
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.025
769
SPS019 Spastic Paraparesis 40 0.025
770
c HMG029 Hemoglobin Se Disease 40 0.025
771
SPR126 Superior Semicircular Canal Dehiscence 39 0.025
772
c ATM075 Autoimmune Encephalitis 39 0.025
773
OVR094 Ovarian Epithelial Cancer 39 0.025
774
P PHT010 Photoparoxysmal Response 1 39 0.025
775
GNT029 Genetic Hypertension 39 0.025
776
HNZ004 Heinz Body Anemias 39 0.025
777
c MJR022 Major Affective Disorder 8 39 0.025
778
MLT001 Multiple Chemical Sensitivity 39 0.025
779
c HRD088 Hereditary Neuropathies 39 0.025
780
ZKV001 Zika Virus Infection 39 0.025
781
HYP610 Hypothyroidism, Central, and Testicular Enlargement 39 0.025
782
ATX010 Ataxia Neuropathy Spectrum 39 0.025
783
NDL001 Nodular Malignant Melanoma 39 0.025
784
EXT007 Extracutaneous Mastocytoma 39 0.025
785
P INT260 Intracranial Berry Aneurysm 38 0.025
786
HRN029 Hearing Loss, Noise-Induced 38 0.025
787
SCR001 Secretory Meningioma 38 0.025
788
RTR001 Retrograde Amnesia 38 0.025
789
MTH064 Methemoglobinemia, Beta-Globin Type 37 0.025
790
SCR011 Scrapie 37 0.025
791
ELP001 Elephantiasis 37 0.025
792
PST010 Pasteurellosis 37 0.025
793
P AXN001 Axonal Neuropathy 36 0.025
794
END072 Endotheliitis 36 0.025
795
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 36 0.025
796
SRF006 Surfactant Dysfunction 36 0.025
797
BRK012 Broken Heart Syndrome 36 0.025
798
P FNC026 Fanconi Renotubular Syndrome 1 36 0.025
799
c CHR682 Chronic Bilirubin Encephalopathy 36 0.025
800
HMM004 Hamamy Syndrome 36 0.025
801
VRL017 Viral Hemorrhagic Fever 36 0.025
802
END011 Endometriosis of Ovary 35 0.025
803
c LKM004 Leukemia, B-Cell, Chronic 35 0.025
804
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 35 0.025
805
P FML187 Familial Hypertension 35 0.025
806
OLG022 Oligoasthenoteratozoospermia 34 0.025
807
BWN006 Bowen's Disease 34 0.025
808
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.025
809
ATY012 Atypical Mycobacteriosis, Familial 34 0.025
810
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.025
811
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 33 0.025
812
CND006 Candida Glabrata 33 0.025
813
CYT014 Cytochrome P450 Oxidoreductase Deficiency 33 0.025
814
MSN003 Mesenteric Vascular Occlusion 33 0.025
815
ATR003 Atrophic Rhinitis 33 0.025
816
CRD016 Cardiac Rupture 33 0.025
817
ART012 Aortitis 33 0.025
818
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 32 0.025
819
MYP035 Myopathy, Distal, with Anterior Tibial Onset 32 0.025
820
TRC020 Tracheitis 32 0.025
821
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 32 0.025
822
RFR009 Refractory Cytopenia with Multilineage Dysplasia 32 0.025
823
ESN009 Eosinophil Peroxidase Deficiency 31 0.025
824
c PRG019 Paragangliomas 2 30 0.025
825
CMP064 Complement Component 3 Deficiency 30 0.025
826
c BLD140 Blood Group, I System 29 0.025
827
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 0.025
828
ANG037 Angiomatosis 29 0.025
829
HRT037 Heart and Brain Malformation Syndrome 28 0.025
830
P ACT232 Acute Necrotizing Encephalopathy 28 0.025
831
P FML340 Familial Episodic Pain Syndrome 28 0.025
832
MNG007 Manganese Poisoning 28 0.025
833
MST020 Mast Cell Activation Syndrome 28 0.025
834
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 28 0.025
835
c THY056 Thyroid Dyshormonogenesis 3 28 0.025
836
KDN013 Kidney Hypertrophy 27 0.025
837
c LNG109 Lung Cancer Susceptibility 1 27 0.025
838
c RNG015 Ring Chromosome 2 27 0.025
839
TXC004 Toxic Diffuse Goiter 27 0.025
840
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 27 0.025
841
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.025
842
MTH071 Methane Production 26 0.025
843
BCL011 Bacillary Angiomatosis 25 0.025
844
TCK004 Tick Infestation 25 0.025
845
c ANM033 Anemia, Sideroblastic, 2, Pyridoxine-Refractory 25 0.025
846
NCL007 Nuclear Gene-Encoded Leigh Syndrome 24 0.025
847
THY020 Thyroid Hyalinizing Trabecular Adenoma 23 0.025
848
CRR012 Cirrhotic Cardiomyopathy 23 0.025
849
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 23 0.025
850
HVY002 Heavy Metal Poisoning 23 0.025
851
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 22 0.025
852
HMG009 Hemoglobin Zurich 22 0.025
853
OBS097 Obsolete: Heinz Body Anemia 22 0.025
854
BNT001 Banti's Syndrome 22 0.025
855
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 21 0.025
856
WRM004 Warm Antibody Hemolytic Anemia 20 0.025
857
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.025
858
BLD137 Blood Group--Ahonen 17 0.025
859
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 15 0.025
860
P ERY016 Erythropoietic Protoporphyria, Autosomal Recessive 13 0.025
861
MYP009 Myopathy with Deficiency of Iscu 12 0.025
862
UNS001 Unstable Hemoglobin Disease 9 0.025
Content
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