Search results for hemoglobin c - beta-thalassemia

368 hits were found for hemoglobin c - beta-thalassemia

# Family MCID Name MIFTS Score
1
c HMG001 Hemoglobin C Disease 39 2.926
2
SCK003 Sickle Cell Anemia 73 2.920
3
P DBT009 Diabetes Mellitus 72 0.241
4
P BRS047 Breast Cancer 100 0.194
5
NRN002 Neuronitis 43 0.162
6
PRS047 Prostatitis 59 0.152
7
P MYC007 Myocardial Infarction 81 0.147
8
P PRS040 Prostate Cancer 88 0.144
9
P HRT032 Heart Disease 80 0.143
10
P CRN018 Coronary Artery Anomaly 69 0.143
11
P NRB001 Neuroblastoma 73 0.141
12
P LNG032 Lung Cancer 99 0.140
13
P CRN300 Coronary Heart Disease 1 57 0.135
14
GST053 Gastric Cancer 84 0.133
15
ART140 Arteries, Anomalies of 51 0.132
16
P CLR023 Colorectal Cancer 98 0.131
17
P ADN016 Adenocarcinoma 71 0.129
18
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.128
19
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.127
20
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.127
21
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.127
22
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.127
23
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.127
24
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.127
25
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.127
26
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.127
27
SQM006 Squamous Cell Carcinoma 74 0.126
28
HYP266 Hypoxia 61 0.126
29
MLN008 Melanoma 72 0.124
30
RTN023 Retinitis 52 0.123
31
P RNG031 Ring Chromosome Y Syndrome 29 0.119
32
GLC008 Glucose Metabolism Disease 38 0.117
33
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.114
34
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.113
35
VSC007 Vascular Disease 71 0.110
36
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.109
37
P ALZ034 Alzheimer Disease 95 0.104
38
PRT036 Peritonitis 67 0.102
39
ISC006 Ischemic Heart Disease 73 0.102
40
P ESP024 Esophagitis 64 0.099
41
c ACT075 Acute Myocardial Infarction 64 0.098
42
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.096
43
HMN044 Human Immunodeficiency Virus Type 1 71 0.095
44
P CRV039 Cervicitis 49 0.094
45
P RHM011 Rheumatoid Arthritis 91 0.091
46
P NRP001 Neuropathy 63 0.090
47
GLB002 Glioblastoma 74 0.088
48
P OVR042 Ovarian Cancer 82 0.087
49
HYP066 Hyperglycemia 64 0.086
50
SQM013 Squamous Cell Carcinoma, Head and Neck 79 0.086
51
P MTH007 Methemoglobinemia 46 0.086
52
c THR092 Thrombophilia Due to Thrombin Defect 61 0.085
53
GST033 Gestational Diabetes 62 0.084
54
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.083
55
GST050 Gastrointestinal System Disease 66 0.083
56
AST005 Asthma 83 0.083
57
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.083
58
MYL069 Myeloma, Multiple 86 0.083
59
P MYC084 Mycobacterium Tuberculosis 1 69 0.081
60
ATM095 Autoimmune Disease 66 0.081
61
SRC014 Sarcoma 68 0.081
62
P CRV035 Cervical Cancer 72 0.081
63
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.080
64
P MCR115 Microvascular Complications of Diabetes 5 66 0.080
65
LNG099 Lung Disease 67 0.079
66
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.078
67
STR067 Stroke, Ischemic 84 0.078
68
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 20 0.077
69
P EXN002 Exanthem 62 0.076
70
ANG054 Angina Pectoris 53 0.076
71
HYP056 Hypoglycemia 62 0.075
72
DMN002 Dementia 68 0.075
73
CYN002 Cyanosis, Transient Neonatal 32 0.074
74
P ENC018 Encephalopathy 58 0.074
75
P LYM026 Lymphoblastic Leukemia 66 0.073
76
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.073
77
PLC008 Placenta Disease 48 0.073
78
c LKM071 Leukemia, Chronic Lymphocytic 75 0.073
79
HMG002 Hemoglobinuria 52 0.071
80
P INF037 Inflammatory Bowel Disease 52 0.071
81
P PLY011 Polycystic Ovary Syndrome 65 0.070
82
P ART021 Arteriosclerosis 62 0.069
83
P NTR004 Neutropenia 60 0.069
84
TRN018 Transitional Cell Carcinoma 58 0.069
85
PRT014 Protein S Deficiency 47 0.069
86
LYM019 Lymphosarcoma 58 0.068
87
P DRR001 Diarrhea 60 0.068
88
PRD007 Periodontal Disease 64 0.067
89
P NSP012 Nasopharyngeal Carcinoma 71 0.067
90
LPD008 Lipid Metabolism Disorder 59 0.067
91
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.066
92
HYP060 Hyperinsulinism 56 0.066
93
ANR040 Aneurysm 61 0.065
94
PLM033 Pulmonary Embolism 62 0.065
95
CLT003 Colitis 63 0.064
96
RSP006 Respiratory System Disease 63 0.063
97
GLC003 Glucose Intolerance 58 0.062
98
PLS007 Plasmodium Falciparum Malaria 59 0.062
99
BRN004 Brain Edema 57 0.061
100
PRP027 Peripheral Vascular Disease 71 0.061
101
SKN016 Skin Disease 68 0.061
102
PLY001 Polycythemia Vera 75 0.061
103
c LKM004 Leukemia, B-Cell, Chronic 37 0.060
104
P CNJ013 Conjunctivitis 67 0.060
105
GT001 Gout 60 0.059
106
GLC006 Galactosemia 64 0.059
107
BRN071 Brain Injury 54 0.059
108
c CNT035 Central Nervous System Disease 65 0.059
109
SKN027 Skin Conditions 48 0.059
110
CHR005 Chorioamnionitis 52 0.059
111
P HYP086 Hypothyroidism 62 0.058
112
P ESS003 Essential Thrombocythemia 71 0.058
113
PHR003 Pharyngitis 59 0.058
114
P END044 Endometriosis 71 0.058
115
P MYL005 Myelofibrosis 75 0.057
116
RFR010 Refractory Anemia 48 0.057
117
c PRC016 Pre-Eclampsia 65 0.057
118
P ECL001 Eclampsia 57 0.056
119
PRP080 Peripheral Artery Disease 54 0.056
120
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 32 0.056
121
P HYP069 Hyperparathyroidism 58 0.055
122
P NRV007 Nervous System Disease 75 0.055
123
BRC085 Brca2 Hereditary Breast and Ovarian Cancer Syndrome 15 0.055
124
P PLM036 Pulmonary Fibrosis 68 0.055
125
MYL031 Myeloproliferative Neoplasm 64 0.055
126
P ENC004 Encephalitis 66 0.054
127
OST017 Osteomyelitis 64 0.054
128
SPN051 Spondylitis 55 0.054
129
CLR108 Colorectal Adenoma 60 0.054
130
P RTN014 Retinal Artery Occlusion 45 0.053
131
DBT083 Diabetes Mellitus, Permanent Neonatal 62 0.053
132
INF009 Inflammatory Spondylopathy 32 0.052
133
c TRC078 Trichohepatoenteric Syndrome 2 34 0.052
134
c MCL042 Macular Degeneration, Age-Related, 1 79 0.052
135
P SYP003 Syphilis 55 0.052
136
P RTN022 Retinal Vein Occlusion 53 0.052
137
LMB062 Limb Ischemia 52 0.051
138
c SPN225 Spondyloarthropathy 1 71 0.051
139
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.051
140
P ALC004 Alcohol Abuse 63 0.051
141
c ACT071 Acute Kidney Failure 54 0.051
142
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 51 0.051
143
P HMR003 Hemorrhagic Disease 61 0.051
144
P PLY014 Polycystic Kidney Disease 60 0.051
145
c THR082 Thrombophilia Due to Activated Protein C Resistance 47 0.051
146
P GST044 Gastritis 61 0.050
147
DSS009 Disseminated Intravascular Coagulation 56 0.050
148
CHR008 Choroiditis 47 0.050
149
BRC012 Brucellosis 71 0.050
150
P KDN017 Kidney Cancer 66 0.050
151
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 60 0.049
152
SCH014 Schistosomiasis 62 0.049
153
DBT010 Diabetic Neuropathy 60 0.048
154
TRM010 Traumatic Brain Injury 54 0.048
155
BNF002 Bone Fracture 56 0.048
156
SHW002 Shwachman-Diamond Syndrome 63 0.048
157
INT002 Intermittent Claudication 61 0.048
158
CRT049 Critical Limb Ischemia 56 0.048
159
CRD223 Cardiac Arrhythmia 52 0.048
160
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 32 0.048
161
MTH009 Mouth Disease 64 0.048
162
GRN017 Granulocytopenia 49 0.048
163
INS001 Insulinoma 66 0.048
164
P TRC086 Trichohepatoenteric Syndrome 1 54 0.048
165
SYS003 Systolic Heart Failure 44 0.048
166
P LTR001 Lateral Sclerosis 58 0.047
167
ANX004 Anoxia 49 0.047
168
LYM067 Lymphoid Leukemia 43 0.047
169
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.047
170
CRT072 Creutzfeldt-Jakob Disease 65 0.047
171
BRS051 Breast Disease 67 0.047
172
P ANT006 Antiphospholipid Syndrome 59 0.047
173
P HYP750 Hypertriglyceridemia, Familial 55 0.047
174
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.047
175
LSH001 Leishmaniasis 71 0.046
176
STM006 Stomach Disease 52 0.046
177
c CNT016 Central Retinal Vein Occlusion 50 0.046
178
P KLZ004 Kala-Azar 1 31 0.046
179
BLD138 Blood Group--Diego System 18 0.046
180
c MCR129 Microvascular Complications of Diabetes 1 62 0.046
181
MLT157 Multiple System Atrophy 1 65 0.046
182
ACT119 Acute Promyelocytic Leukemia 64 0.046
183
BRN080 Brain Ischemia 45 0.046
184
SDD001 Sudden Infant Death Syndrome 61 0.045
185
CRB004 Cerebral Artery Occlusion 46 0.045
186
c MCR112 Microvascular Complications of Diabetes 2 30 0.045
187
APL001 Aplastic Anemia 74 0.045
188
BRN028 Brain Cancer 72 0.045
189
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.045
190
P LCT001 Lactic Acidosis 51 0.045
191
PLM001 Pulmonary Tuberculosis 72 0.044
192
P BPL003 Bipolar Disorder 61 0.044
193
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 27 0.044
194
c ERY048 Erythrocytosis, Familial, 2 48 0.044
195
STM007 Stomatitis 52 0.044
196
BDD001 Budd-Chiari Syndrome 58 0.043
197
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.043
198
c LSS005 Lissencephaly 1 46 0.043
199
P SCL057 Scoliosis, Isolated 1 28 0.043
200
HLL004 Hellp Syndrome 53 0.043
201
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.042
202
c ACT210 Acute Respiratory Distress Syndrome 63 0.042
203
P LPR021 Leprosy 3 59 0.042
204
ANT009 Antithrombin Iii Deficiency 58 0.042
205
RHM001 Rheumatic Fever 59 0.042
206
P PYL005 Pyelonephritis 56 0.042
207
INT007 Intermediate Coronary Syndrome 55 0.042
208
RHM035 Rheumatic Fever-Related Antigen 34 0.042
209
P RSP003 Respiratory Failure 71 0.041
210
VNW001 Von Willebrand's Disease 61 0.041
211
P AGG001 Aggressive Periodontitis 55 0.041
212
CRV040 Cervix Carcinoma 52 0.041
213
PLS009 Plasma Cell Neoplasm 51 0.041
214
c ALZ056 Alzheimer Disease 3 41 0.041
215
c ANM048 Anemia, Congenital Dyserythropoietic, Type Iv 26 0.041
216
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 24 0.041
217
c DMN006 Diamond-Blackfan Anemia 3 22 0.041
218
SPT004 Septic Arthritis 60 0.041
219
CHL067 Cholecystitis 58 0.041
220
c ACT134 Acute Liver Failure 52 0.041
221
DBT062 Diabetic Foot Ulcers 59 0.040
222
ADP007 Adie Pupil 41 0.040
223
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.040
224
c CNT028 Central Retinal Artery Occlusion 40 0.040
225
ATN005 Autonomic Dysfunction 51 0.040
226
P DNG005 Dengue Virus 56 0.039
227
URM002 Uremia 52 0.039
228
FCT001 Factor Viii Deficiency 50 0.039
229
ISC002 Ischemic Optic Neuropathy 48 0.039
230
P DYS021 Dysautonomia 47 0.039
231
MRB003 Morbid Obesity 61 0.039
232
PST095 Post-Thrombotic Syndrome 52 0.039
233
ADN001 Adenosine Deaminase Deficiency 52 0.039
234
c ACT042 Acute Pyelonephritis 48 0.039
235
TRN015 Transient Cerebral Ischemia 58 0.038
236
PRT082 Preterm Premature Rupture of the Membranes 51 0.038
237
PLC007 Placental Abruption 50 0.038
238
P DMY001 Demyelinating Polyneuropathy 46 0.038
239
c ART101 Aortic Valve Disease 2 65 0.037
240
P ATR005 Atrophic Gastritis 51 0.037
241
CRB085 Cerebral Hemorrhage 47 0.037
242
CRT015 Carotid Artery Occlusion 42 0.037
243
SPN185 Spinal Cord Infarction 33 0.037
244
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 16 0.037
245
c EXD008 Exudative Vitreoretinopathy 1 65 0.036
246
P HMR012 Hemorrhagic Fever 60 0.036
247
RSP002 Respiratory Syncytial Virus Infectious Disease 53 0.036
248
THR016 Thrombophlebitis 53 0.036
249
FCT006 Factor V Deficiency 52 0.036
250
HMC014 Homocysteinemia 49 0.036
251
ALP077 Alpha-Methylacetoacetic Aciduria 41 0.036
252
CRY036 Cryptogenic Cirrhosis 34 0.036
253
APH001 Aphthous Stomatitis 64 0.035
254
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.035
255
ORL004 Oral Submucous Fibrosis 56 0.035
256
GRW007 Growth Hormone Deficiency 52 0.035
257
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 51 0.035
258
ATN002 Autonomic Nervous System Disease 51 0.035
259
P HML033 Hemolytic Uremic Syndrome, Atypical 1 49 0.035
260
HDN002 Head Injury 48 0.035
261
ALX002 Alexithymia 40 0.035
262
CRV069 Cervix Disease 39 0.035
263
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 60 0.035
264
P MRC003 Mercury Poisoning 50 0.035
265
KWS001 Kwashiorkor 43 0.035
266
GGN002 Gigantism 36 0.035
267
ATS009 Autosomal Genetic Disease 31 0.035
268
HML052 Hemolytic Anemia, Nonspherocytic, Due to Hexokinase Deficiency 22 0.035
269
VSC003 Visceral Leishmaniasis 59 0.034
270
RBR001 Roberts Syndrome 55 0.034
271
P UTR058 Uterine Anomalies 55 0.034
272
HMN032 Human Herpesvirus 8 50 0.034
273
GNG011 Gingival Disease 50 0.034
274
SDD008 Sudden Sensorineural Hearing Loss 46 0.034
275
RTN021 Retinal Vascular Occlusion 45 0.034
276
c DNG003 Dengue Disease 66 0.033
277
GLS001 Gliosarcoma 61 0.033
278
PTN001 Patent Foramen Ovale 58 0.033
279
VSC002 Vascular Dementia 58 0.033
280
STR020 Strabismus 55 0.033
281
LPR001 Lepromatous Leprosy 53 0.033
282
INT075 Intracranial Hypertension 53 0.033
283
MCL006 Macular Retinal Edema 51 0.033
284
P AFB001 Afibrinogenemia 49 0.033
285
DBT008 Diabetic Angiopathy 48 0.033
286
SYN036 Syncope 46 0.033
287
THR035 Thrombasthenia 46 0.033
288
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 36 0.033
289
SGT001 Sagittal Sinus Thrombosis 34 0.033
290
c ELL005 Elliptocytosis 2 29 0.033
291
PHS014 Phosphoglycerate Kinase 1 Deficiency 29 0.033
292
DNG002 Dengue Hemorrhagic Fever 66 0.032
293
P CLC063 Celiac Disease 1 65 0.032
294
SND001 Sandhoff Disease 65 0.032
295
P INT030 Intracranial Aneurysm 58 0.032
296
P MCR010 Microcephaly 57 0.032
297
CRN030 Coronary Stenosis 52 0.032
298
PRT129 Prothrombin Deficiency, Congenital 51 0.032
299
P DYS026 Dysfibrinogenemia 51 0.032
300
NSD001 Nose Disease 51 0.032
301
RTN003 Retinal Ischemia 50 0.032
302
NRR001 Neuroretinitis 46 0.032
303
CRD137 Cardiogenic Shock 45 0.032
304
ISC015 Ischemic Colitis 39 0.032
305
FRN014 Fournier Gangrene 38 0.032
306
GLS018 Glass Syndrome 38 0.032
307
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 36 0.032
308
CHR178 Chromosomal Triplication 35 0.032
309
NSP003 Nasopharyngeal Disease 34 0.032
310
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 33 0.032
311
BRN056 Bronchopulmonary Dysplasia 61 0.030
312
URN003 Urinary Schistosomiasis 50 0.030
313
c PRD040 Periodontitis, Chronic 49 0.030
314
ANC001 Ancylostomiasis 48 0.030
315
ESP002 Esophageal Varix 46 0.030
316
PRT012 Prothrombin Deficiency 46 0.030
317
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 39 0.030
318
PRP028 Peripheral Vertigo 37 0.030
319
c CTR174 Cataract 40 33 0.030
320
CRB132 Cerebral Sinovenous Thrombosis 32 0.030
321
PRC051 Paracetamol Poisoning 30 0.030
322
SCH037 Schinzel-Giedion Midface Retraction Syndrome 28 0.030
323
ULC005 Ulcer of Lower Limbs 23 0.030
324
c CTR025 Cataract, Total Congenital 20 0.030
325
P DYS007 Dyskeratosis Congenita 68 0.029
326
FCT003 Factor X Deficiency 58 0.029
327
c MYT020 Myotonic Dystrophy 2 56 0.029
328
GST037 Gastroparesis 56 0.029
329
RTC002 Reticular Dysgenesis 53 0.029
330
ACH005 Achalasia 52 0.029
331
P PRN026 Porencephaly 50 0.029
332
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 49 0.029
333
SND002 Sneddon Syndrome 48 0.029
334
VND001 Vein Disease 48 0.029
335
SCT005 Scott Syndrome 48 0.029
336
PRD004 Prediabetes Syndrome 46 0.029
337
P SLL003 Salla Disease 43 0.029
338
PHM001 Phimosis 41 0.029
339
P ANX007 Anauxetic Dysplasia 1 36 0.029
340
LVD002 Livedoid Vasculopathy 36 0.029
341
FNT004 Fainting 36 0.029
342
SPN331 Spondyloocular Syndrome 34 0.029
343
ACT056 Acute Cor Pulmonale 34 0.029
344
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 0.029
345
c HML035 Hemolytic Uremic Syndrome, Atypical 2 22 0.029
346
c CRT085 Carotid Intimal Medial Thickness 2 21 0.029
347
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.026
348
TWN001 Twin-to-Twin Transfusion Syndrome 51 0.026
349
EXP004 Exophthalmos 50 0.026
350
ESN011 Eisenmenger Syndrome 49 0.026
351
FTL021 Fetal Macrosomia 46 0.026
352
ALB002 Albinism 45 0.026
353
c CHR546 Chronic Mountain Sickness 45 0.026
354
PRC003 Proctitis 44 0.026
355
BCL002 B Cell Deficiency 44 0.026
356
MCR017 Macrocytic Anemia 44 0.026
357
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.026
358
PRL019 Prolidase Deficiency 41 0.026
359
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 37 0.026
360
BYS001 Byssinosis 33 0.026
361
TST007 Testicular Infarct 28 0.026
362
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 25 0.026
363
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 21 0.026
364
c TRC117 Trichothiodystrophy 6, Nonphotosensitive 20 0.026
365
c DMN028 Diamond-Blackfan Anemia 12 19 0.026
366
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 16 0.026
367
P STM009 Stomatocytosis I 16 0.026
368
HMG024 Hemoglobinopathy Toms River 6 0.026
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