Search results for heme

860 hits were found for heme

# Family MCID Name MIFTS Score
1
HMX003 Heme Oxygenase 1 Deficiency 27 7.868
2
c PRT132 Protoporphyria, Erythropoietic, 1 61 4.640
3
P PRP029 Porphyria 62 3.089
4
ISC004 Ischemia 58 0.257
5
IRN002 Iron Metabolism Disease 57 0.257
6
HLX001 Helix Syndrome 47 0.241
7
DFC004 Deficiency Anemia 70 0.229
8
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.217
9
ERY051 Erythroleukemia, Familial 56 0.206
10
BLR008 Bilirubin Metabolic Disorder 57 0.194
11
HYP266 Hypoxia 57 0.190
12
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.187
13
P VSC007 Vascular Disease 63 0.187
14
P SCK005 Sickle Cell Disease 50 0.187
15
P ALZ034 Alzheimer Disease 88 0.179
16
c PRC016 Pre-Eclampsia 63 0.177
17
HMS001 Hemosiderosis 54 0.174
18
ATH013 Atherosclerosis Susceptibility 65 0.172
19
P RRH023 Rare Hereditary Hemochromatosis 41 0.170
20
IRN001 Iron Deficiency Anemia 59 0.158
21
HMP009 Haemophilus Influenzae 43 0.158
22
MLR004 Malaria 81 0.154
23
PRP083 Porphyria, Acute Intermittent 64 0.154
24
P KDN018 Kidney Disease 72 0.150
25
P HML002 Hemolytic Anemia 63 0.150
26
P CLR023 Colorectal Cancer 99 0.148
27
P THL005 Thalassemia 60 0.148
28
c ACT071 Acute Kidney Failure 60 0.144
29
P SDR003 Sideroblastic Anemia 49 0.142
30
P PLM037 Pulmonary Hypertension 67 0.133
31
P PRD008 Periodontitis 64 0.133
32
c ACT078 Acute Porphyria 51 0.133
33
HYP066 Hyperglycemia 61 0.129
34
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.126
35
P LVR013 Liver Disease 68 0.119
36
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.117
37
BRN071 Brain Injury 49 0.117
38
LVR012 Liver Cirrhosis 62 0.114
39
CHG001 Chagas Disease 66 0.111
40
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.111
41
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.109
42
P PRP003 Porphyria Cutanea Tarda 67 0.109
43
P MYL006 Myeloid Leukemia 60 0.109
44
CYT002 Cytokine Deficiency 42 0.109
45
P PRK057 Parkinson Disease, Late-Onset 78 0.106
46
P NRB001 Neuroblastoma 72 0.106
47
CLT003 Colitis 62 0.106
48
ALL014 Allergic Encephalomyelitis 38 0.106
49
P CRD246 Cardiovascular System Disease 57 0.103
50
P INF037 Inflammatory Bowel Disease 54 0.103
51
TRM010 Traumatic Brain Injury 51 0.103
52
P PLM036 Pulmonary Fibrosis 65 0.100
53
CRB004 Cerebral Artery Occlusion 45 0.100
54
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.100
55
ATM095 Autoimmune Disease 62 0.097
56
c ACT027 Acute Pancreatitis 60 0.097
57
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.097
58
NNT012 Neonatal Jaundice 53 0.097
59
SCK003 Sickle Cell Anemia 74 0.094
60
c LKM063 Leukemia, Chronic Myeloid 72 0.094
61
LPP008 Lipoprotein Quantitative Trait Locus 62 0.094
62
CHL068 Cholestasis 61 0.094
63
FTT001 Fatty Liver Disease 61 0.094
64
PRT013 Portal Hypertension 59 0.094
65
BCT022 Bacterial Infectious Disease 56 0.094
66
VRG001 Variegate Porphyria 56 0.094
67
HMG005 Hemoglobinopathy 56 0.094
68
PRP082 Porphyria, Congenital Erythropoietic 56 0.094
69
48X005 48,xyyy 39 0.094
70
P PHC003 Pheochromocytoma 71 0.091
71
c CHR684 Chronic Kidney Disease 70 0.091
72
LSH001 Leishmaniasis 63 0.091
73
TXC005 Toxic Shock Syndrome 62 0.091
74
SPN186 Spinal Cord Injury 60 0.091
75
c MCR113 Microvascular Complications of Diabetes 3 52 0.091
76
ART140 Arteries, Anomalies of 52 0.091
77
c MCR120 Microvascular Complications of Diabetes 7 47 0.091
78
ADR040 Adrenal Gland Pheochromocytoma 46 0.091
79
P KLZ004 Kala-Azar 1 41 0.091
80
c MCR130 Microvascular Complications of Diabetes 6 41 0.091
81
c MCR133 Microvascular Complications of Diabetes 4 41 0.091
82
P LNG032 Lung Cancer 98 0.088
83
P LNG064 Lung Cancer Susceptibility 3 78 0.088
84
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.088
85
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.088
86
P CRN300 Coronary Heart Disease 1 63 0.088
87
LNG099 Lung Disease 60 0.088
88
c ACT134 Acute Liver Failure 56 0.088
89
BRN004 Brain Edema 56 0.088
90
c HMC039 Hemochromatosis, Type 1 74 0.084
91
c HPT073 Hepatitis C Virus 72 0.084
92
P GLM045 Glioma 63 0.084
93
ANT024 Anthrax Disease 58 0.084
94
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.084
95
c PRD040 Periodontitis, Chronic 53 0.084
96
BNR002 Bone Resorption Disease 48 0.084
97
GLL048 Glial Tumor 45 0.084
99
P HRT032 Heart Disease 75 0.081
100
c BTT014 Beta-Thalassemia 74 0.081
101
CNG034 Congestive Heart Failure 69 0.081
102
P LKM002 Leukemia 68 0.081
103
PRT037 Pertussis 65 0.081
104
c HPT001 Hepatitis C 62 0.081
105
LMB062 Limb Ischemia 55 0.081
106
PLM010 Pulmonary Edema 54 0.081
107
NTR046 Neutrophil Migration 50 0.081
108
ANX004 Anoxia 40 0.081
109
P GST053 Gastric Cancer 83 0.077
110
GLB015 Glioblastoma Multiforme 75 0.077
111
MYL009 Myelodysplastic Syndrome 70 0.077
112
PRT036 Peritonitis 64 0.077
113
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.077
114
CPR004 Coproporphyria, Hereditary 57 0.077
115
NNL006 Non-Alcoholic Steatohepatitis 54 0.077
116
HMG002 Hemoglobinuria 50 0.077
117
RNL077 Renal Fibrosis 47 0.077
118
PPL052 Papillomatosis, Confluent and Reticulated 33 0.077
119
P BRS047 Breast Cancer 97 0.073
120
P PNC035 Pancreatic Cancer 84 0.073
121
P BLD134 Bladder Cancer 79 0.073
122
c HYP836 Hypercholesterolemia, Familial, 1 73 0.073
123
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.073
124
P DRM053 Dermatitis, Atopic 66 0.073
125
ORL011 Oral Cancer 60 0.073
126
P GLM007 Glomerulonephritis 57 0.073
127
P NRP001 Neuropathy 56 0.073
128
END086 End Stage Renal Disease 51 0.073
129
RTN003 Retinal Ischemia 50 0.073
130
P ECL001 Eclampsia 50 0.073
131
CTN011 Cutaneous Porphyria 38 0.073
132
ESP021 Esophageal Cancer 90 0.069
133
c LKM061 Leukemia, Acute Myeloid 84 0.069
134
SVR004 Severe Combined Immunodeficiency 73 0.069
135
OTT002 Otitis Media 72 0.069
136
P MYC007 Myocardial Infarction 70 0.069
137
P DMN001 Diamond-Blackfan Anemia 69 0.069
138
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.069
139
SQM006 Squamous Cell Carcinoma 60 0.069
140
P DNG005 Dengue Virus 59 0.069
141
P RHN004 Rhinitis 57 0.069
142
c ACT075 Acute Myocardial Infarction 57 0.069
143
ALL006 Allergic Asthma 56 0.069
144
GST037 Gastroparesis 54 0.069
145
P ART021 Arteriosclerosis 54 0.069
146
47X002 47,xyy 49 0.069
147
c INH020 Inherited Metabolic Disorder 47 0.069
148
ORL015 Oral Squamous Cell Carcinoma 43 0.069
149
HYP001 Hypochromic Microcytic Anemia 38 0.069
150
c HYP595 Hypertension, Essential 84 0.064
151
STR067 Stroke, Ischemic 81 0.064
152
ULC004 Ulcerative Colitis 73 0.064
153
P GRF003 Graft-Versus-Host Disease 72 0.064
154
LGH007 Leigh Syndrome 70 0.064
155
ART016 Aortic Aneurysm 69 0.064
156
ALL003 Allergic Rhinitis 67 0.064
157
P HYP098 Hypereosinophilic Syndrome 67 0.064
158
P MCR115 Microvascular Complications of Diabetes 5 66 0.064
159
P DBT009 Diabetes Mellitus 64 0.064
160
SKN016 Skin Disease 63 0.064
161
P PSR002 Psoriasis 62 0.064
162
ALL026 Allergic Hypersensitivity Disease 62 0.064
163
DPH001 Diphtheria 60 0.064
164
P TYR004 Tyrosinemia 58 0.064
165
P BCL017 B-Cell Lymphoma 58 0.064
166
THR024 Thrombosis 57 0.064
167
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.064
168
P HMC002 Homocystinuria 53 0.064
169
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.064
170
IMP005 Impotence 52 0.064
171
URM002 Uremia 49 0.064
172
MCR018 Microcytic Anemia 47 0.064
173
URT010 Ureteral Obstruction 45 0.064
174
c HRM022 Hair Morphology 1 11 0.064
175
P HPT023 Hepatocellular Carcinoma 100 0.060
176
KPS004 Kaposi Sarcoma 75 0.060
177
P SLP006 Sleep Apnea 69 0.060
178
P PNM007 Pneumonia 68 0.060
179
CRB039 Cerebrovascular Disease 67 0.060
180
c SML038 Small Cell Cancer of the Lung 65 0.060
181
P ADN016 Adenocarcinoma 64 0.060
182
LPD008 Lipid Metabolism Disorder 62 0.060
183
P PNC044 Pancreatitis 61 0.060
184
BRN056 Bronchopulmonary Dysplasia 57 0.060
185
P HML001 Hemolytic-Uremic Syndrome 53 0.060
186
PRP080 Peripheral Artery Disease 53 0.060
187
c VRL010 Viral Hepatitis 52 0.060
188
PST011 Pustulosis of Palm and Sole 52 0.060
189
P AST007 Astrocytoma 51 0.060
190
P RNV001 Renovascular Hypertension 48 0.060
191
RDC006 Red Cell Aplasia 43 0.060
192
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.060
193
P PRS040 Prostate Cancer 97 0.054
194
IMM167 Immune Deficiency Disease 78 0.054
195
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.054
196
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.054
197
P RSP003 Respiratory Failure 74 0.054
198
P HNT016 Huntington Disease 72 0.054
199
P HPT021 Hepatitis 67 0.054
200
P OLG002 Oligodendroglioma 67 0.054
201
ANG054 Angina Pectoris 66 0.054
202
P NTR004 Neutropenia 63 0.054
203
TRN015 Transient Cerebral Ischemia 63 0.054
204
P END044 Endometriosis 63 0.054
205
c OPT053 Optic Atrophy 1 63 0.054
206
P VSC011 Vasculitis 62 0.054
207
GST033 Gestational Diabetes 61 0.054
208
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.054
209
VSL002 Visual Epilepsy 59 0.054
210
BRN002 Bronchiolitis 59 0.054
211
ANR040 Aneurysm 59 0.054
212
c ANM036 Anemia, Sideroblastic, 1 57 0.054
213
DSS009 Disseminated Intravascular Coagulation 57 0.054
214
P PLY018 Polycythemia 56 0.054
215
P SZR006 Seizure Disorder 56 0.054
216
AGN016 Aging 56 0.054
217
BRN012 Bronchiolitis Obliterans 55 0.054
218
HYP060 Hyperinsulinism 54 0.054
219
GLC003 Glucose Intolerance 54 0.054
220
DBT010 Diabetic Neuropathy 54 0.054
221
SLP001 Sleeping Sickness 54 0.054
222
DYS015 Dysentery 52 0.054
223
c ACT135 Acute Graft Versus Host Disease 52 0.054
224
ENT011 Enterocolitis 51 0.054
225
SPL018 Splenomegaly 48 0.054
226
P PRR002 Pure Red-Cell Aplasia 47 0.054
227
P KRN004 Kernicterus 47 0.054
228
CHR074 Choriocarcinoma 47 0.054
229
ACT003 Acute Kidney Tubular Necrosis 45 0.054
230
PST036 Posterior Column Ataxia with Retinitis Pigmentosa 38 0.054
231
PST040 Posterior Column Ataxia 23 0.054
232
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.049
233
c SYS001 Systemic Lupus Erythematosus 86 0.049
234
MYL069 Myeloma, Multiple 85 0.049
236
P ATX030 Ataxia-Telangiectasia 82 0.049
237
CYS001 Cystic Fibrosis 81 0.049
238
P RTN008 Retinitis Pigmentosa 79 0.049
239
INS024 Insulin-Like Growth Factor I 79 0.049
240
c ATR087 Atrial Standstill 1 75 0.049
241
c THR092 Thrombophilia Due to Thrombin Defect 73 0.049
242
P HYP061 Hypertrophic Cardiomyopathy 70 0.049
243
P CRD119 Cardiac Arrest 67 0.049
244
P MSC005 Muscular Dystrophy 66 0.049
245
KWS002 Kawasaki Disease 65 0.049
246
CLN015 Colon Adenocarcinoma 65 0.049
247
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.049
248
CTN007 Cutaneous Leishmaniasis 62 0.049
249
DRM006 Dermatitis 61 0.049
250
P KDN017 Kidney Cancer 60 0.049
251
P NPH012 Nephrotic Syndrome 60 0.049
252
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.049
253
P MYC008 Myocarditis 59 0.049
254
MTC097 Mitochondrial Complex Iv Deficiency 59 0.049
255
ADN018 Adenoma 59 0.049
256
PPT005 Peptic Ulcer Disease 59 0.049
257
c ACT073 Acute Leukemia 58 0.049
258
GLB001 Gilbert Syndrome 58 0.049
259
P PRP019 Peripheral Nervous System Disease 58 0.049
260
MCR013 Microphthalmia 57 0.049
261
VSC003 Visceral Leishmaniasis 55 0.049
262
P PLM034 Pulmonary Emphysema 55 0.049
263
PRP030 Purpura 54 0.049
264
P LTR001 Lateral Sclerosis 54 0.049
265
HMC014 Homocysteinemia 53 0.049
266
PLS007 Plasmodium Falciparum Malaria 52 0.049
267
TLN003 Telangiectasis 52 0.049
268
ILS001 Ileus 51 0.049
269
THR016 Thrombophlebitis 51 0.049
270
PLC008 Placenta Disease 50 0.049
271
TRY001 Trypanosomiasis 50 0.049
272
P OBS001 Obstructive Jaundice 50 0.049
273
P CLL015 Collagen Disease 47 0.049
274
LYM019 Lymphosarcoma 46 0.049
275
RTN023 Retinitis 46 0.049
276
P BNG032 Benign Mesothelioma 46 0.049
277
c PCH010 Pachyonychia Congenita 3 44 0.049
278
NRR001 Neuroretinitis 42 0.049
279
PST092 Posttransplant Acute Limbic Encephalitis 29 0.049
280
NRL016 Neural Tube Defects 82 0.042
281
OST012 Osteoarthritis 78 0.042
282
P MDL005 Medulloblastoma 77 0.042
283
AST005 Asthma 76 0.042
284
CRV035 Cervical Cancer 76 0.042
285
c SPN225 Spondyloarthropathy 1 73 0.042
286
P RTN024 Retinoblastoma 73 0.042
287
MSC157 Muscular Dystrophy, Duchenne Type 72 0.042
288
P MLT020 Multiple Sclerosis 72 0.042
289
HMN044 Human Immunodeficiency Virus Type 1 71 0.042
290
PRP027 Peripheral Vascular Disease 71 0.042
291
P AMY004 Amyloidosis 70 0.042
292
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.042
293
P LYM118 Lymphoma 68 0.042
294
CHL065 Cholangiocarcinoma 68 0.042
295
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.042
296
P INF038 Influenza 68 0.042
297
P THR014 Thrombocytopenia 67 0.042
298
P SKN015 Skin Carcinoma 66 0.042
299
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.042
300
P ADL010 Adult Respiratory Distress Syndrome 65 0.042
301
ART002 Arts Syndrome 64 0.042
302
P RHB003 Rhabdomyosarcoma 63 0.042
303
PLG002 Plague 63 0.042
304
P ART023 Arthropathy 62 0.042
305
c ANM038 Anemia, Autoimmune Hemolytic 62 0.042
306
c SCL052 Scleroderma, Familial Progressive 61 0.042
307
P ENC018 Encephalopathy 61 0.042
308
YLL002 Yellow Fever 61 0.042
309
P ENC004 Encephalitis 61 0.042
310
VRL011 Viral Infectious Disease 61 0.042
311
HPT019 Hepatic Encephalopathy 60 0.042
312
ACQ007 Acquired Immunodeficiency Syndrome 60 0.042
313
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.042
314
c HPT016 Hepatitis B 59 0.042
315
c DNG003 Dengue Disease 59 0.042
316
PLM033 Pulmonary Embolism 59 0.042
317
PRN019 Perinatal Necrotizing Enterocolitis 59 0.042
318
P BRS044 Breast Adenocarcinoma 59 0.042
319
CRY005 Cryptococcosis 58 0.042
320
P UVT001 Uveitis 57 0.042
321
P EXN002 Exanthem 57 0.042
322
SCH014 Schistosomiasis 57 0.042
323
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.042
324
GST050 Gastrointestinal System Disease 56 0.042
325
SLC006 Silicosis 56 0.042
326
P GST044 Gastritis 56 0.042
327
HPT022 Hepatoblastoma 56 0.042
328
FLR001 Filarial Elephantiasis 55 0.042
329
P HYP076 Hyperthyroidism 55 0.042
330
FLR002 Filariasis 55 0.042
331
INT007 Intermediate Coronary Syndrome 55 0.042
332
P ALP008 Alopecia 54 0.042
333
PRS045 Prostatic Hypertrophy 53 0.042
334
P MNC007 Monocytic Leukemia 53 0.042
335
GSG001 Gas Gangrene 53 0.042
336
c FML008 Familial Retinoblastoma 53 0.042
337
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.042
338
P RCT021 Rectum Cancer 52 0.042
339
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.042
340
THR004 Thrombocytosis 51 0.042
341
OCL069 Ocular Motor Apraxia 51 0.042
342
PRS021 Prostatic Adenoma 51 0.042
343
INT079 Intrahepatic Cholangiocarcinoma 51 0.042
344
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.042
345
ACT017 Acute Chest Syndrome 51 0.042
346
c SVR005 Severe Pre-Eclampsia 50 0.042
347
AZS001 Azoospermia 50 0.042
348
ENT004 Enthesopathy 49 0.042
349
PRS129 Prostatic Hyperplasia, Benign 49 0.042
350
HPT009 Hepatopulmonary Syndrome 48 0.042
351
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.042
352
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.042
353
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.042
354
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.042
355
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.042
356
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.042
357
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.042
358
HPT004 Hepatic Coma 45 0.042
359
c HMG003 Hemoglobin E Disease 45 0.042
360
P CHR345 Chronic Pain 44 0.042
361
SBC016 Subacute Delirium 44 0.042
362
P SDR002 Siderosis 44 0.042
363
MCR017 Macrocytic Anemia 44 0.042
364
CVD001 Covid-19 44 0.042
365
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.042
366
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.042
367
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.042
368
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.042
369
GST020 Gastric Antral Vascular Ectasia 41 0.042
370
WLL004 Wallerian Degeneration 39 0.042
371
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.042
372
c CRD219 Cardiomyopathy, Infantile Hypertrophic 32 0.042
373
PRT094 Protoporphyria, Erythropoietic, X-Linked 31 0.042
374
MCL057 Macular Dystrophy with Central Cone Involvement 31 0.042
375
MTC150 Mitochondrial Complex V Deficiency, Mitochondrial Type 1 29 0.042
376
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.042
377
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.042
378
PRQ002 Paraquat Poisoning 26 0.042
379
P HRM021 Hair Morphology 2 22 0.042
380
c PRT135 Protoporphyria, Erythropoietic, 2 18 0.042
381
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.034
382
P OVR042 Ovarian Cancer 88 0.034
383
P RHM011 Rheumatoid Arthritis 80 0.034
384
c DLT002 Dilated Cardiomyopathy 79 0.034
385
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.034
386
END057 Endometrial Cancer 74 0.034
387
LPT014 Leptin Deficiency or Dysfunction 74 0.034
388
c MNN043 Meningioma, Familial 74 0.034
389
P CNR004 Cone-Rod Dystrophy 2 73 0.034
390
P FML011 Familial Adenomatous Polyposis 72 0.034
391
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.034
392
P MYP004 Myopathy 70 0.034
393
PLM001 Pulmonary Tuberculosis 69 0.034
394
P MLN008 Melanoma 69 0.034
395
P LKM062 Leukemia, Acute Lymphoblastic 69 0.034
396
CNN005 Connective Tissue Disease 68 0.034
397
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.034
398
c HMP029 Hemophilia a 67 0.034
399
P CHR012 Chronic Granulomatous Disease 67 0.034
400
P BLD062 Bile Duct Cancer 67 0.034
401
c RHB024 Rhabdomyosarcoma 2 67 0.034
402
c TYR012 Tyrosinemia, Type I 66 0.034
403
OST159 Osteogenic Sarcoma 66 0.034
404
HYP056 Hypoglycemia 66 0.034
405
P ATR011 Atrial Fibrillation 66 0.034
406
P HYD006 Hydrocephalus 66 0.034
407
P HRS035 Hirschsprung Disease 1 65 0.034
408
SRC014 Sarcoma 65 0.034
409
c JVN010 Juvenile Rheumatoid Arthritis 64 0.034
410
GT001 Gout 64 0.034
411
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.034
412
BRC012 Brucellosis 64 0.034
413
DGR001 Digeorge Syndrome 64 0.034
414
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.034
415
c ACT068 Acute Cystitis 63 0.034
416
c ALP101 Alpha-Thalassemia 62 0.034
417
c SVR001 Severe Acute Respiratory Syndrome 62 0.034
418
P ESP024 Esophagitis 62 0.034
419
MNN042 Meningioma, Radiation-Induced 62 0.034
420
NTR005 Nutritional Deficiency Disease 62 0.034
421
ALC006 Alcoholic Hepatitis 61 0.034
422
P HMN010 Hemangioma 61 0.034
423
RGH009 Right Atrial Isomerism 60 0.034
424
c JVN061 Juvenile Arthritis 60 0.034
425
P TXP001 Toxoplasmosis 60 0.034
426
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.034
427
P ALP009 Alopecia Areata 60 0.034
428
DNG002 Dengue Hemorrhagic Fever 60 0.034
429
P CTR002 Cataract 60 0.034
430
HYD002 Hydronephrosis 60 0.034
431
SPP011 Suppression of Tumorigenicity 12 59 0.034
432
CHL014 Cholera 59 0.034
433
THY029 Thyroid Carcinoma 59 0.034
434
CHL123 Chlamydia 59 0.034
435
GNG013 Gingivitis 59 0.034
436
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.034
437
GST045 Gastroenteritis 59 0.034
438
CNT047 Contact Dermatitis 58 0.034
439
P MTR012 Mitral Valve Disease 58 0.034
440
EYD002 Eye Disease 58 0.034
441
CNS004 Constipation 58 0.034
442
P INF032 Infertility 57 0.034
443
P PLY041 Polymyositis 57 0.034
444
c MST023 Mesothelioma, Malignant 57 0.034
445
P FCL005 Focal Segmental Glomerulosclerosis 57 0.034
446
CMM005 Common Cold 57 0.034
447
VSC002 Vascular Dementia 57 0.034
448
PLC005 Placental Insufficiency 57 0.034
449
PHR003 Pharyngitis 57 0.034
450
P FBR017 Fibrosarcoma 56 0.034
451
P PLY011 Polycystic Ovary Syndrome 56 0.034
452
HYP005 Hypokalemia 55 0.034
453
ORL004 Oral Submucous Fibrosis 55 0.034
454
P DRR001 Diarrhea 55 0.034
455
DFF005 Diffuse Large B-Cell Lymphoma 55 0.034
456
HNC001 Henoch-Schoenlein Purpura 55 0.034
457
SYN007 Synovitis 54 0.034
458
PPL022 Papilloma 54 0.034
459
SNS003 Sensory Peripheral Neuropathy 54 0.034
460
CLR030 Clear Cell Renal Cell Carcinoma 53 0.034
461
MST005 Mastitis 53 0.034
462
SPN035 Spindle Cell Sarcoma 53 0.034
463
P FBR031 Febrile Seizures 53 0.034
464
PRN011 Pernicious Anemia 53 0.034
465
c GLL024 Gallbladder Disease 1 53 0.034
466
P RTN018 Retinal Disease 53 0.034
467
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.034
468
ONC002 Onchocerciasis 52 0.034
469
SPN051 Spondylitis 51 0.034
470
P HMP007 Hemophilia 51 0.034
471
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.034
472
CLR109 Colorectal Adenocarcinoma 51 0.034
473
P THR015 Thrombophilia 51 0.034
474
P MMB011 Membranous Nephropathy 50 0.034
475
SPN021 Spinal Meningioma 50 0.034
476
P ESN008 Eosinophilic Pneumonia 50 0.034
477
VLV047 Volvulus of Midgut 49 0.034
478
SPT005 Spotted Fever 49 0.034
479
MTC005 Mitochondrial Metabolism Disease 49 0.034
480
ATS010 Autosomal Recessive Disease 48 0.034
481
RFR010 Refractory Anemia 48 0.034
482
PLM035 Pulmonary Eosinophilia 48 0.034
483
IGG001 Iga Glomerulonephritis 48 0.034
484
DGN001 Degenerative Disc Disease 48 0.034
485
P PRP056 Porphyria, Acute Hepatic 48 0.034
486
PRP007 Priapism 47 0.034
487
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.034
488
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.034
489
TST044 Testicular Torsion 47 0.034
490
ATN005 Autonomic Dysfunction 46 0.034
491
MYC005 Myocardial Stunning 46 0.034
492
P BRB001 Beriberi 46 0.034
493
SQM002 Squamous Cell Papilloma 46 0.034
494
c MLG068 Malignant Glioma 46 0.034
495
CLN044 Colon Adenoma 44 0.034
496
MDD018 Middle East Respiratory Syndrome 43 0.034
497
OBS082 Obstructive Nephropathy 42 0.034
498
SCR001 Secretory Meningioma 41 0.034
499
CHN002 Chancroid 40 0.034
500
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 40 0.034
501
CRB086 Cerebral Aneurysms 40 0.034
502
CRN020 Coronary Restenosis 39 0.034
503
RCK002 Rocky Mountain Spotted Fever 39 0.034
504
AML001 Amelanotic Melanoma 39 0.034
505
SPR066 Superficial Siderosis 39 0.034
506
BTN004 Biotin Deficiency 38 0.034
507
THR123 Thrombotic Microangiopathy 36 0.034
508
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.034
509
PLC002 Plica Syndrome 36 0.034
510
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.034
511
PRM329 Premature Aging 35 0.034
512
FST010 Fasting Hypoglycemia 35 0.034
513
c LKM005 Leukemia, T-Cell, Chronic 34 0.034
514
INF009 Inflammatory Spondylopathy 31 0.034
515
FTL004 Fetal Erythroblastosis 31 0.034
516
CHL079 Children's Interstitial Lung Disease 26 0.034
517
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 25 0.034
518
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.034
519
ANT078 Antipyrine Metabolism 24 0.034
520
FWL003 Fowler Urethral Sphincter Dysfunction Syndrome 20 0.034
521
LWF001 Low-Flow Priapism 19 0.034
522
XLN067 X-Linked Protoporphyria 16 0.034
523
c FNC027 Fanconi Anemia, Complementation Group a 81 0.024
524
P LKM071 Leukemia, Chronic Lymphocytic 79 0.024
525
GST019 Gastrointestinal Stromal Tumor 78 0.024
526
P APL001 Aplastic Anemia 74 0.024
527
CRH001 Crohn's Disease 74 0.024
528
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.024
529
AGM019 Agammaglobulinemia, X-Linked 71 0.024
530
GST040 Gastric Adenocarcinoma 70 0.024
531
c PNC108 Pancreatitis, Hereditary 70 0.024
532
PLY001 Polycythemia Vera 69 0.024
533
LYM133 Lymphoma, Hodgkin, Classic 69 0.024
534
P HYP086 Hypothyroidism 69 0.024
535
P ANG001 Angelman Syndrome 69 0.024
536
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.024
537
P SYS005 Systemic Scleroderma 68 0.024
538
P MYC084 Mycobacterium Tuberculosis 1 68 0.024
539
c BSL007 Basal Cell Carcinoma 68 0.024
540
SKN019 Skin Melanoma 68 0.024
541
BRN024 Bronchitis 68 0.024
542
MLD001 Melioidosis 68 0.024
543
P FRN006 Frontotemporal Dementia 68 0.024
544
P NSP012 Nasopharyngeal Carcinoma 66 0.024
545
c MCR129 Microvascular Complications of Diabetes 1 66 0.024
546
LNG039 Lung Squamous Cell Carcinoma 66 0.024
547
P NRV007 Nervous System Disease 66 0.024
548
GTL001 Gitelman Syndrome 65 0.024
549
P AGM001 Agammaglobulinemia 65 0.024
550
P MTR014 Motor Neuron Disease 65 0.024
551
c ART101 Aortic Valve Disease 2 65 0.024
552
IRR002 Irritable Bowel Syndrome 65 0.024
553
P HRP006 Herpes Simplex 65 0.024
554
c WLM013 Wilms Tumor 1 65 0.024
555
P THY023 Thymoma 65 0.024
556
P CHR071 Charcot-Marie-Tooth Disease 65 0.024
557
APN008 Apnea, Obstructive Sleep 64 0.024
558
NRM005 Neuromuscular Disease 64 0.024
559
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.024
560
TBC004 Tobacco Addiction 64 0.024
561
CLR108 Colorectal Adenoma 64 0.024
562
P FRD001 Friedreich Ataxia 64 0.024
563
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.024
564
MSC007 Muscle Hypertrophy 64 0.024
565
LYM017 Lyme Disease 64 0.024
566
OST017 Osteomyelitis 64 0.024
567
c DPH024 Diaphragmatic Hernia, Congenital 63 0.024
568
P ANR048 Aniridia 1 63 0.024
569
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.024
570
P HYP069 Hyperparathyroidism 63 0.024
571
ACT119 Acute Promyelocytic Leukemia 63 0.024
572
ANR007 Anorexia Nervosa 63 0.024
573
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.024
574
c LCL006 Localized Scleroderma 62 0.024
575
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.024
576
HMT002 Hematologic Cancer 62 0.024
577
P PLY014 Polycystic Kidney Disease 62 0.024
578
c BRN108 Branchiootic Syndrome 1 62 0.024
579
P HYP750 Hypertriglyceridemia, Familial 62 0.024
580
P TRC086 Trichohepatoenteric Syndrome 1 62 0.024
581
P PRM006 Primary Biliary Cirrhosis 62 0.024
583
OST003 Osteonecrosis 61 0.024
584
c WLM018 Wilms Tumor 5 61 0.024
585
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 61 0.024
586
RTN017 Retinal Detachment 61 0.024
587
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.024
588
PNM010 Pneumothorax, Primary Spontaneous 60 0.024
589
SZR001 Sezary's Disease 60 0.024
590
ACN002 Acanthosis Nigricans 60 0.024
591
VRC005 Varicose Veins 60 0.024
592
STT001 Status Epilepticus 60 0.024
593
P BND020 Bone Disease 59 0.024
594
P LKD001 Leukodystrophy 59 0.024
595
IGR001 Ige Responsiveness, Atopic 59 0.024
596
P SLP005 Sleep Disorder 59 0.024
597
P CYS018 Cystitis 59 0.024
598
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.024
599
AVN001 Avian Influenza 59 0.024
600
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.024
601
HLC007 Helicobacter Pylori Infection 59 0.024
602
ALK013 Alkaptonuria 58 0.024
603
SPT004 Septic Arthritis 58 0.024
604
c PRM005 Primary Hyperparathyroidism 58 0.024
605
ADL030 Adult-Onset Still's Disease 58 0.024
606
P BNC003 Bone Cancer 58 0.024
607
LYM027 Lymphopenia 58 0.024
608
P CND004 Candidiasis 58 0.024
609
BRG013 Buerger Disease 58 0.024
610
EXT034 Extrinsic Allergic Alveolitis 58 0.024
611
MXD005 Mixed Connective Tissue Disease 58 0.024
612
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.024
613
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.024
614
P END033 Endocarditis 57 0.024
615
c LKM070 Leukemia, Acute Monocytic 57 0.024
616
HMR039 Hemorrhage, Intracerebral 57 0.024
617
CYT008 Cytomegalovirus Infection 57 0.024
618
JPN002 Japanese Encephalitis 57 0.024
619
P BPL003 Bipolar Disorder 56 0.024
620
P PYL005 Pyelonephritis 56 0.024
621
PNM008 Pneumothorax 56 0.024
622
P ADL017 Adult T-Cell Leukemia 56 0.024
623
TCK001 Tick-Borne Encephalitis 56 0.024
624
LST001 Listeriosis 56 0.024
625
ADN027 Adenomyosis 56 0.024
626
c ESS001 Essential Tremor 56 0.024
627
P MTC069 Mitochondrial Disorders 56 0.024
628
ALL010 Allergic Contact Dermatitis 56 0.024
629
SBC001 Subacute Sclerosing Panencephalitis 56 0.024
630
INT030 Intracranial Aneurysm 56 0.024
631
P HYP024 Hypoparathyroidism 56 0.024
632
P PLY019 Polyneuropathy 56 0.024
633
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.024
634
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.024
635
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.024
636
P MLN007 Male Infertility 55 0.024
637
P SLM003 Salmonellosis 55 0.024
638
AMN003 Amnestic Disorder 54 0.024
639
P RST001 Restless Legs Syndrome 54 0.024
640
CRY003 Cryptosporidiosis 54 0.024
641
BRN014 Bronchopneumonia 54 0.024
642
THR013 Thoracic Outlet Syndrome 54 0.024
643
c PST005 Posterior Uveitis 54 0.024
644
HLL004 Hellp Syndrome 54 0.024
645
P TRM003 Tremor 54 0.024
646
PNC001 Pancytopenia 54 0.024
647
c HNT010 Huntington Disease-Like 1 53 0.024
648
PST046 Post-Transplant Lymphoproliferative Disease 53 0.024
649
c DMN023 Diamond-Blackfan Anemia 1 53 0.024
650
P INS002 in Situ Carcinoma 53 0.024
651
P RTN016 Retinal Degeneration 53 0.024
652
OCL006 Ocular Hypertension 53 0.024
653
INF034 Infective Endocarditis 53 0.024
654
GTR002 Goiter 53 0.024
655
TXC002 Toxic Encephalopathy 53 0.024
656
INT051 Intussusception 53 0.024
657
TRC003 Trichomoniasis 53 0.024
658
ALC009 Alcoholic Liver Cirrhosis 53 0.024
659
P INT068 Intestinal Disease 53 0.024
660
c CNT035 Central Nervous System Disease 52 0.024
661
EXP004 Exophthalmos 52 0.024
662
NRT004 Neuritis 52 0.024
663
CRT016 Carotid Artery Disease 52 0.024
664
P MSC003 Muscular Atrophy 52 0.024
665
c THY107 Thymoma, Familial 52 0.024
666
PPT001 Peptic Esophagitis 52 0.024
667
ACT200 Acute Monoblastic Leukemia 52 0.024
668
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.024
669
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.024
670
P TRT010 Teratoma 52 0.024
671
PNG002 Pain Agnosia 51 0.024
673
P SPP010 Suppressor of Tumorigenicity 3 51 0.024
674
P PLG001 Pelger-Huet Anomaly 51 0.024
675
c PNC106 Pancreatic Agenesis 1 51 0.024
676
P LCT001 Lactic Acidosis 51 0.024
677
ESP002 Esophageal Varix 51 0.024
678
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.024
679
TNG007 Tongue Carcinoma 51 0.024
680
TLR001 Tularemia 51 0.024
681
PNM005 Pneumonic Plague 51 0.024
682
HYP781 Hypoascorbemia 51 0.024
683
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.024
684
CHR005 Chorioamnionitis 51 0.024
685
PLR007 Pleural Empyema 50 0.024
686
P FNC004 Fanconi Syndrome 50 0.024
687
HPT014 Hepatorenal Syndrome 50 0.024
688
CRN030 Coronary Stenosis 50 0.024
689
P MTR003 Mitral Valve Stenosis 50 0.024
690
MCP006 Mucoepidermoid Carcinoma 50 0.024
691
P TMP001 Temporal Lobe Epilepsy 50 0.024
692
c AMY009 Amyloidosis Aa 50 0.024
693
c THR071 Thrombocytopenia 1 50 0.024
694
P KRT007 Keratoconus 50 0.024
695
c LRG001 Large Cell Carcinoma 50 0.024
696
LSS003 Lassa Fever 50 0.024
697
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 50 0.024
698
RBF001 Riboflavin Deficiency 49 0.024
699
c CHR418 Chronic Leukemia 49 0.024
700
P IGN003 Iga Nephropathy 1 49 0.024
701
SYS003 Systolic Heart Failure 49 0.024
702
CVR006 Cavernous Hemangioma 49 0.024
703
VRC001 Varicocele 49 0.024
704
SLD003 Sialadenitis 49 0.024
705
MNN009 Meningoencephalitis 49 0.024
706
P CTN015 Cutaneous T Cell Lymphoma 49 0.024
707
VCC001 Vaccinia 49 0.024
708
SBP001 Subependymal Giant Cell Astrocytoma 49 0.024
709
c HRD026 Hereditary Ataxia 48 0.024
710
ACT098 Acute Erythroid Leukemia 48 0.024
711
PNC034 Pancreas Disease 48 0.024
712
BBS001 Babesiosis 48 0.024
713
END062 Endometrial Hyperplasia 48 0.024
714
OPD006 Opioid Addiction 48 0.024
715
PYL006 Pyloric Stenosis 48 0.024
716
P MRC003 Mercury Poisoning 48 0.024
717
c MLG069 Malignant Hypertension 47 0.024
718
KHN001 Kuhnt-Junius Degeneration 47 0.024
719
IRN004 Iron-Refractory Iron Deficiency Anemia 47 0.024
720
ZKF001 Zika Fever 47 0.024
721
P OVR046 Ovarian Cyst 47 0.024
722
PHS021 Phosphoglycerate Dehydrogenase Deficiency 47 0.024
723
TTH006 Tooth Disease 46 0.024
724
P MTH007 Methemoglobinemia 46 0.024
725
P HMR005 Hemorrhoid 46 0.024
726
TCL003 T Cell Deficiency 46 0.024
727
GST010 Gestational Trophoblastic Neoplasm 46 0.024
728
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.024
729
OLG001 Oligospermia 45 0.024
730
RTR008 Root Resorption 45 0.024
731
c TRC022 Tricuspid Valve Insufficiency 45 0.024
732
CYN002 Cyanosis, Transient Neonatal 45 0.024
733
CRT015 Carotid Artery Occlusion 45 0.024
734
RTR001 Retrograde Amnesia 44 0.024
735
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.024
736
ART012 Aortitis 44 0.024
737
ISC015 Ischemic Colitis 44 0.024
738
NDL001 Nodular Malignant Melanoma 44 0.024
739
PRM003 Premature Ejaculation 44 0.024
740
OVR063 Overnutrition 44 0.024
741
ART006 Arthus Reaction 44 0.024
742
c PRM038 Primary Agammaglobulinemia 44 0.024
743
P MYG005 Myoglobinuria 44 0.024
744
CRB090 Cerebral Hypoxia 44 0.024
745
LMY003 Leiomyomatosis 43 0.024
746
RFR003 Refractive Error 43 0.024
747
TST015 Testicular Disease 43 0.024
748
c CHR546 Chronic Mountain Sickness 43 0.024
749
MYC013 Mycobacterium Abscessus 43 0.024
750
DNG001 Dengue Shock Syndrome 43 0.024
751
MST004 Mast Cell Neoplasm 42 0.024
753
P PHT010 Photoparoxysmal Response 1 42 0.024
754
ACR009 Acromesomelic Dysplasia, Hunter-Thompson Type 41 0.024
755
CTS002 Cat-Scratch Disease 41 0.024
756
ELP001 Elephantiasis 41 0.024
757
VLV010 Vulvovaginitis 41 0.024
758
c FML015 Familial Nephrotic Syndrome 41 0.024
759
c MJR024 Major Affective Disorder 9 41 0.024
760
BBN001 Bubonic Plague 41 0.024
761
P HYP009 Hypertrophic Pyloric Stenosis 41 0.024
762
c MCR112 Microvascular Complications of Diabetes 2 41 0.024
763
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 40 0.024
764
INT060 Intestinal Atresia 40 0.024
765
c HMG001 Hemoglobin C Disease 40 0.024
766
P FNC034 Fanconi Renotubular Syndrome 2 40 0.024
767
SPR126 Superior Semicircular Canal Dehiscence 40 0.024
768
PLY100 Polyploidy 40 0.024
769
MLT001 Multiple Chemical Sensitivity 40 0.024
770
HNZ004 Heinz Body Anemias 39 0.024
771
c FNC026 Fanconi Renotubular Syndrome 1 39 0.024
772
P INT260 Intracranial Berry Aneurysm 39 0.024
773
HST016 Histiocytic Sarcoma 39 0.024
774
LKP003 Leukoplakia 39 0.024
775
HYP856 Hypothyroidism, Central, with Testicular Enlargement 39 0.024
776
PCH007 Pouchitis 39 0.024
777
P FML340 Familial Episodic Pain Syndrome 39 0.024
778
END011 Endometriosis of Ovary 39 0.024
779
c HMG029 Hemoglobin Se Disease 39 0.024
780
c CHR682 Chronic Bilirubin Encephalopathy 39 0.024
781
SCR011 Scrapie 39 0.024
782
EXT007 Extracutaneous Mastocytoma 38 0.024
783
c ATM075 Autoimmune Encephalitis 38 0.024
784
OVR094 Ovarian Epithelial Cancer 38 0.024
785
SPS019 Spastic Paraparesis 38 0.024
786
c MJR022 Major Affective Disorder 8 38 0.024
787
P FML187 Familial Hypertension 37 0.024
788
CRD016 Cardiac Rupture 37 0.024
789
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 37 0.024
790
GLM044 Glomerular Disease 37 0.024
791
HRN029 Hearing Loss, Noise-Induced 37 0.024
792
c HRD088 Hereditary Neuropathies 37 0.024
793
HMM004 Hamamy Syndrome 37 0.024
794
ART010 Arteriolosclerosis 37 0.024
795
VRL017 Viral Hemorrhagic Fever 36 0.024
796
TRC020 Tracheitis 36 0.024
797
INT020 Intravenous Leiomyomatosis 36 0.024
798
HMN004 Hemangioma of Liver 36 0.024
799
P AXN001 Axonal Neuropathy 36 0.024
800
OLG022 Oligoasthenoteratozoospermia 36 0.024
801
BRK012 Broken Heart Syndrome 35 0.024
802
ATR003 Atrophic Rhinitis 35 0.024
803
SRF006 Surfactant Dysfunction 35 0.024
804
MTH064 Methemoglobinemia, Beta-Globin Type 35 0.024
805
END072 Endotheliitis 35 0.024
806
ATY012 Atypical Mycobacteriosis, Familial 35 0.024
807
ATX010 Ataxia Neuropathy Spectrum 34 0.024
808
CMP064 Complement Component 3 Deficiency 34 0.024
809
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.024
810
PST010 Pasteurellosis 34 0.024
811
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 33 0.024
812
ACT064 Acute Necrotizing Encephalitis 33 0.024
813
BWN006 Bowen's Disease 32 0.024
814
CND006 Candida Glabrata 32 0.024
815
KDN013 Kidney Hypertrophy 32 0.024
816
c BLD140 Blood Group, I System 32 0.024
817
MYP035 Myopathy, Distal, with Anterior Tibial Onset 32 0.024
818
CYT014 Cytochrome P450 Oxidoreductase Deficiency 32 0.024
819
c INC031 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 3 32 0.024
820
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.024
821
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.024
822
HRT037 Heart and Brain Malformation Syndrome 31 0.024
823
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.024
824
BCL011 Bacillary Angiomatosis 31 0.024
825
c PRG019 Paragangliomas 2 31 0.024
826
ESN009 Eosinophil Peroxidase Deficiency 30 0.024
827
c THY056 Thyroid Dyshormonogenesis 3 30 0.024
828
FTL068 Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 30 0.024
829
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 30 0.024
830
MNG007 Manganese Poisoning 29 0.024
831
TRN004 Trench Fever 29 0.024
832
IDP093 Idiopathic Gastroparesis 29 0.024
833
HYP346 Hypotrichosis and Recurrent Skin Vesicles 28 0.024
834
ANG037 Angiomatosis 28 0.024
835
TCK004 Tick Infestation 28 0.024
836
c INC035 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 3 27 0.024
837
c LNG109 Lung Cancer Susceptibility 1 27 0.024
838
MSN003 Mesenteric Vascular Occlusion 27 0.024
839
MST020 Mast Cell Activation Syndrome 26 0.024
840
c RNG015 Ring Chromosome 2 26 0.024
841
c ATS210 Autosomal Recessive Sideroblastic Anemia 26 0.024
842
MTH071 Methane Production 26 0.024
843
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.024
844
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.024
845
CRR012 Cirrhotic Cardiomyopathy 24 0.024
846
TXC004 Toxic Diffuse Goiter 24 0.024
847
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.024
848
HMG009 Hemoglobin Zurich 22 0.024
849
HVY002 Heavy Metal Poisoning 22 0.024
850
NCL007 Nuclear Gene-Encoded Leigh Syndrome 22 0.024
851
CRD158 Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2 22 0.024
852
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.024
853
BNT001 Banti's Syndrome 21 0.024
854
WRM004 Warm Antibody Hemolytic Anemia 20 0.024
855
HRD090 Harderoporphyria 20 0.024
856
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.024
857
BLD137 Blood Group--Ahonen 16 0.024
858
P ERY016 Erythropoietic Protoporphyria, Autosomal Recessive 12 0.024
859
MYP009 Myopathy with Deficiency of Iscu 12 0.024
860
UNS001 Unstable Hemoglobin Disease 8 0.024
Content
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