Search results for hemoglobin c - beta-thalassemia

434 hits were found for hemoglobin c - beta-thalassemia

# Family MCID Name MIFTS Score
1
c HMG001 Hemoglobin C Disease 47 6.214
2
SCK003 Sickle Cell Anemia 71 3.039
3
c VRL010 Viral Hepatitis 60 0.216
4
P BRS047 Breast Cancer 100 0.175
5
NRN002 Neuronitis 41 0.149
6
HMG012 Hemoglobin Constant Spring 18 0.143
7
PRS047 Prostatitis 56 0.138
8
P PRS040 Prostate Cancer 90 0.131
9
P MYC007 Myocardial Infarction 79 0.130
10
P NRB001 Neuroblastoma 70 0.127
11
P LNG032 Lung Cancer 95 0.123
12
P CLR023 Colorectal Cancer 97 0.116
13
CSY001 C Syndrome 50 0.114
14
RTN023 Retinitis 50 0.113
15
ATH003 Atherosclerosis 65 0.112
16
GST053 Gastric Cancer 78 0.112
17
MLN008 Melanoma 62 0.112
18
P OBS005 Obesity 92 0.112
19
HMG025 Hemoglobin H Disease, Nondeletional 39 0.112
20
SQM006 Squamous Cell Carcinoma 70 0.112
21
HV1006 Hiv-1 80 0.112
22
HYP266 Hypoxia 56 0.110
23
P ADN016 Adenocarcinoma 69 0.109
24
c HPT015 Hepatitis D 52 0.109
25
ART111 Artery Disease 55 0.107
26
P CRN211 Coronary Artery Disease 74 0.106
27
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.103
28
P HYP607 Hypercholesterolemia, Familial 76 0.102
29
c ACT075 Acute Myocardial Infarction 60 0.095
30
PRT036 Peritonitis 63 0.093
31
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.093
32
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.093
33
P RNL014 Renal Cell Carcinoma 82 0.092
34
ACQ007 Acquired Immunodeficiency Syndrome 60 0.091
35
P ESP024 Esophagitis 61 0.091
36
GLC008 Glucose Metabolism Disease 42 0.090
37
HMG009 Hemoglobin Zurich 16 0.088
38
P MTH007 Methemoglobinemia 45 0.085
39
P CRV039 Cervicitis 45 0.084
40
IMP003 Impaired Renal Function Disease 34 0.084
41
MDY003 Mody, Type Ii 36 0.083
42
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.083
43
LPD008 Lipid Metabolism Disorder 58 0.082
44
c HMG029 Hemoglobin Se Disease 28 0.080
45
c HPT007 Hepatitis E 54 0.079
46
TBR010 Tuberculosis 70 0.079
47
P GLB002 Glioblastoma 68 0.079
48
P NRP001 Neuropathy 59 0.078
49
P OVR042 Ovarian Cancer 76 0.078
50
GST033 Gestational Diabetes 57 0.078
51
VSC007 Vascular Disease 67 0.077
52
HYP066 Hyperglycemia 61 0.075
53
P MLT019 Multiple Myeloma 83 0.074
54
URN009 Urinary System Disease 50 0.073
55
SRC014 Sarcoma 66 0.073
56
P URF003 Urofacial Syndrome 1 50 0.073
57
P AST005 Asthma 82 0.073
58
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.073
59
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.071
60
HMG014 Hemoglobin Quong Sze 7 0.070
61
HYP056 Hypoglycemia 61 0.069
62
PRP027 Peripheral Vascular Disease 68 0.068
63
DMN002 Dementia 65 0.068
64
P PLY018 Polycythemia 58 0.067
65
ISC006 Ischemic Heart Disease 68 0.067
66
HMG002 Hemoglobinuria 48 0.067
67
c CHR090 Chronic Lymphocytic Leukemia 76 0.066
68
P INF037 Inflammatory Bowel Disease 63 0.065
69
SXL003 Sexual Disorder 42 0.065
70
c PND001 Pain Disorder 54 0.065
71
VSC011 Vasculitis 62 0.064
72
ANG054 Angina Pectoris 50 0.064
73
P MCR129 Microvascular Complications of Diabetes 1 54 0.064
74
P PLY011 Polycystic Ovary Syndrome 65 0.063
75
PLS007 Plasmodium Falciparum Malaria 55 0.063
76
P LYM026 Lymphoblastic Leukemia 62 0.062
77
P NTR004 Neutropenia 59 0.062
78
ADL002 Adult Syndrome 52 0.062
79
PRD007 Periodontal Disease 60 0.062
80
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.062
81
P DRR001 Diarrhea 60 0.062
82
IMM071 Immunodeficiency 12 26 0.061
83
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.061
84
P NSP012 Nasopharyngeal Carcinoma 66 0.061
85
TRN018 Transitional Cell Carcinoma 53 0.061
86
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.060
87
PLM033 Pulmonary Embolism 60 0.060
88
P HYP060 Hyperinsulinism 58 0.060
89
PRT014 Protein S Deficiency 53 0.059
90
P EXN002 Exanthem 57 0.059
91
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.058
92
GLC003 Glucose Intolerance 55 0.058
93
MRF001 Marfan Syndrome 73 0.058
94
c CNT068 Central Pain Syndrome 29 0.058
95
CLT003 Colitis 60 0.058
96
VTM003 Vitamin Metabolic Disorder 30 0.058
97
LNG099 Lung Disease 64 0.057
98
IMM076 Immunodeficiency 24 27 0.057
99
ANR040 Aneurysm 57 0.057
100
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 9 0.057
101
c ATM011 Autoimmune Hepatitis 60 0.057
102
BRN004 Brain Edema 52 0.056
103
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.056
104
HPT074 Hepatic Adenoma, Somatic 50 0.055
105
HNM002 Hinman Syndrome 25 0.055
106
ATM052 Autoimmune Disease 1 25 0.055
107
HYD038 Hydrops Fetalis, Nonimmune 40 0.055
108
STR067 Stroke, Ischemic 75 0.055
109
CHR005 Chorioamnionitis 48 0.055
110
GLC006 Galactosemia 64 0.055
111
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.055
112
c CRN174 Coronary Heart Disease 2 20 0.054
113
P PLM036 Pulmonary Fibrosis 71 0.054
114
PHR003 Pharyngitis 56 0.054
115
P GT001 Gout 58 0.053
116
P ALC004 Alcohol Abuse 59 0.053
117
P ESS003 Essential Thrombocythemia 70 0.053
118
ATM053 Autoimmune Disease 2 16 0.053
119
P END044 Endometriosis 66 0.053
120
c TRC078 Trichohepatoenteric Syndrome 2 29 0.052
121
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.052
122
c THR092 Thrombophilia Due to Thrombin Defect 54 0.051
123
P FML035 Familial Hyperlipidemia 48 0.051
124
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 51 0.051
125
SCH014 Schistosomiasis 58 0.051
126
SPN051 Spondylitis 51 0.051
127
LRN003 Learning Disability 49 0.051
128
P HYP069 Hyperparathyroidism 58 0.051
129
PLC008 Placenta Disease 33 0.051
130
P CLR108 Colorectal Adenoma 60 0.050
131
c PRC016 Pre-Eclampsia 56 0.050
132
ATM014 Autoimmune Disease of Endocrine System 36 0.050
133
P CNJ013 Conjunctivitis 64 0.050
134
P DBT083 Diabetes Mellitus, Permanent Neonatal 55 0.050
135
MSC004 Muscle Tissue Disease 34 0.050
136
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.049
137
P ENC004 Encephalitis 63 0.049
138
P ECL001 Eclampsia 54 0.049
139
CYN002 Cyanosis, Transient Neonatal 28 0.049
140
P HYP086 Hypothyroidism 64 0.049
141
VSC006 Vascular Cancer 51 0.048
142
OST017 Osteomyelitis 61 0.048
143
c MYC058 Myocardial Infarction 2 28 0.048
144
SKN023 Skin Tag 44 0.048
145
P SYP003 Syphilis 53 0.048
146
LYM019 Lymphosarcoma 53 0.048
147
BRN071 Brain Injury 52 0.047
148
RFR010 Refractory Anemia 45 0.047
149
P PLY019 Polyneuropathy 56 0.047
150
P MYL005 Myelofibrosis 67 0.047
151
SYS003 Systolic Heart Failure 43 0.047
152
ART016 Aortic Aneurysm 69 0.046
153
P PLY014 Polycystic Kidney Disease 53 0.046
154
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.046
155
HPY002 H. Pylori Infection 61 0.046
156
P GST044 Gastritis 56 0.046
157
TXC005 Toxic Shock Syndrome 60 0.045
158
PLS009 Plasma Cell Neoplasm 48 0.045
159
INT002 Intermittent Claudication 56 0.045
160
CHL067 Cholecystitis 57 0.045
161
CHR008 Choroiditis 44 0.045
162
P NRV006 Nervous System Cancer 60 0.045
163
LMB062 Limb Ischemia 48 0.044
164
P HYP117 Hypertriglyceridemia 61 0.044
165
RSP006 Respiratory System Disease 58 0.044
166
BRN080 Brain Ischemia 41 0.044
167
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.044
168
GNG011 Gingival Disease 46 0.044
169
ACD009 Acid-Labile Subunit, Deficiency of 45 0.044
170
ATN002 Autonomic Nervous System Disease 48 0.044
171
ATM012 Autoimmune Disease of Blood 35 0.044
172
ATM055 Autoimmune Disease 4 15 0.044
173
BNF002 Bone Fracture 50 0.043
174
BCL002 B Cell Deficiency 49 0.043
175
c ADL001 Adult Lymphoma 39 0.043
176
P CRT072 Creutzfeldt-Jakob Disease 61 0.043
177
INS001 Insulinoma 61 0.043
178
DBT010 Diabetic Neuropathy 55 0.043
179
ATN005 Autonomic Dysfunction 49 0.043
180
CRB025 Carbohydrate Metabolic Disorder 46 0.043
181
P RTN014 Retinal Artery Occlusion 44 0.043
182
ADP007 Adie Pupil 34 0.043
183
MDY005 Mody, Type I 30 0.043
184
GRN017 Granulocytopenia 44 0.043
185
c THR037 Thrombocytopenia 2 35 0.043
186
P SDD001 Sudden Infant Death Syndrome 61 0.043
187
HNZ001 Heinz Body Anemia 39 0.043
188
P RSP003 Respiratory Failure 71 0.042
189
LSH001 Leishmaniasis 66 0.042
190
RNL101 Renal Cell Carcinoma, Papillary 63 0.042
191
NSY001 N Syndrome 36 0.042
192
APH001 Aphthous Stomatitis 62 0.042
193
ATR060 Atrial Standstill, Digenic 51 0.042
194
MLT021 Multiple System Atrophy 70 0.042
195
SLP005 Sleep Disorder 53 0.042
196
RDN001 Reading Disorder 34 0.042
197
P HMR012 Hemorrhagic Fever 56 0.041
198
ANM001 Anemia of Prematurity 41 0.041
199
P LPR003 Leprosy 69 0.041
200
P BPL003 Bipolar Disorder 62 0.041
201
c TYP024 Type Ii Mixed Cryoglobulinemia 33 0.041
202
CRV047 Cervical Cancer, Somatic 65 0.040
203
ALC007 Alcohol Dependence 63 0.040
204
P LCT001 Lactic Acidosis 51 0.040
205
c CHR418 Chronic Leukemia 47 0.040
206
AYM001 Ayme-Gripp Syndrome 41 0.040
207
c DRR009 Diarrhea 6 29 0.040
208
BRC012 Brucellosis 66 0.040
209
SPT004 Septic Arthritis 60 0.040
210
KRT002 Keratomalacia 52 0.040
211
STM007 Stomatitis 50 0.040
212
P INT063 Intellectual Disability 49 0.040
213
FML039 Female Reproductive System Disease 48 0.040
214
BRS051 Breast Disease 61 0.039
215
P SZR006 Seizure Disorder 56 0.039
216
c ACT071 Acute Kidney Failure 49 0.039
217
HYP099 Hyperferritinemia-Cataract Syndrome 42 0.039
218
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.039
219
P CLC005 Celiac Disease 68 0.039
220
SHW002 Shwachman-Diamond Syndrome 61 0.039
221
RHM001 Rheumatic Fever 54 0.039
222
P PYL005 Pyelonephritis 52 0.039
223
CRT049 Critical Limb Ischemia 51 0.039
224
SHH001 Sheehan Syndrome 44 0.039
225
c HYP595 Hypertension, Essential 69 0.038
226
MYL031 Myeloproliferative Neoplasm 58 0.038
227
VGT001 Vogt-Koyanagi-Harada Disease 54 0.038
228
TTH006 Tooth Disease 52 0.038
229
KLD001 Keloids 51 0.038
230
P AGG001 Aggressive Periodontitis 50 0.038
231
c CNG415 Congenital Disorder of Glycosylation, Type Ia 45 0.038
232
CRB004 Cerebral Artery Occlusion 45 0.038
233
CRT015 Carotid Artery Occlusion 43 0.038
234
c THR048 Thrombocytopenia 4 26 0.038
235
TRM010 Traumatic Brain Injury 52 0.038
236
c CNG206 Congenital Disorder of Glycosylation, Type Ie 47 0.038
237
CRB085 Cerebral Hemorrhage 46 0.038
238
PRP021 Peripheral Nervous System Neoplasm 46 0.038
239
MXD023 Mixed Cell Type Cancer 44 0.038
240
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.038
241
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.038
242
SNS023 Sensory System Cancer 43 0.037
243
ISL010 Isolated 17-Linked Lissencephaly 28 0.037
244
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.037
245
MND006 Mondor Disease 21 0.037
246
DNG002 Dengue Hemorrhagic Fever 63 0.036
247
DBT062 Diabetic Foot Ulcers 51 0.036
248
c ACT042 Acute Pyelonephritis 45 0.036
249
c CNT028 Central Retinal Artery Occlusion 37 0.036
250
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 36 0.036
251
FRN014 Fournier Gangrene 35 0.036
252
FRB001 Farber Lipogranulomatosis 53 0.036
253
HYP457 Hypertrophic Scars 45 0.036
254
CRZ001 Crouzon Syndrome 70 0.036
255
BLL006 Bullous Pemphigoid 59 0.036
256
P RBL001 Rubella 57 0.036
257
TRN015 Transient Cerebral Ischemia 56 0.036
258
CRV040 Cervix Carcinoma 53 0.036
259
P DMY001 Demyelinating Polyneuropathy 43 0.036
260
HML006 Hemolytic Anemia Due to G6pd Deficiency 33 0.036
261
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.035
262
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 22 0.035
263
P ANR002 Aniridia 64 0.035
264
ESP020 Esophageal Atresia 50 0.035
265
URM002 Uremia 48 0.035
266
P TRC086 Trichohepatoenteric Syndrome 1 48 0.035
267
LYM067 Lymphoid Leukemia 44 0.035
268
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 43 0.035
269
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.034
270
P SHR029 Short Syndrome 58 0.034
271
P END033 Endocarditis 54 0.034
272
CRN030 Coronary Stenosis 51 0.034
273
GRW007 Growth Hormone Deficiency 50 0.034
274
FML038 Female Reproductive Organ Cancer 50 0.034
275
P ATR005 Atrophic Gastritis 45 0.034
276
P DYS021 Dysautonomia 44 0.034
277
PTY001 Pityriasis Rosea 42 0.034
278
P CHL066 Cholangitis 42 0.034
279
ORL004 Oral Submucous Fibrosis 51 0.033
280
INT007 Intermediate Coronary Syndrome 50 0.033
281
SDD007 Sudden Cardiac Death 47 0.033
282
BLL004 Bullous Keratopathy 44 0.033
283
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.033
284
PRN049 Paraneoplastic Pemphigus 40 0.033
285
ALX002 Alexithymia 37 0.033
286
ATM015 Autoimmune Disease of Gastrointestinal Tract 34 0.033
287
c LKM004 Leukemia, B-Cell, Chronic 24 0.033
288
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.033
289
GLC009 Glucosephosphate Dehydrogenase Deficiency 41 0.033
290
PRS036 Parasitic Protozoa Infectious Disease 41 0.033
291
ANM030 Anemia, Hypochromic Microcytic 36 0.033
292
c DMN006 Diamond-Blackfan Anemia 3 29 0.033
293
SPN331 Spondyloocular Syndrome 27 0.033
294
c DYS168 Dyserythropoietic Anemia, Congenital, Type Iv 25 0.033
295
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.032
296
P RCK004 Rickets 61 0.032
297
VSC003 Visceral Leishmaniasis 56 0.032
298
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 55 0.032
299
P MTC069 Mitochondrial Disorders 53 0.032
300
CRV069 Cervix Disease 32 0.032
301
c AST037 Asthma 1 28 0.032
302
MNT045 Montefiore Syndrome 10 0.032
303
ART017 Aortic Disease 57 0.031
304
GLS001 Gliosarcoma 55 0.031
305
VSC002 Vascular Dementia 54 0.031
306
P STR020 Strabismus 51 0.031
307
FML037 Female Breast Cancer 50 0.031
308
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.031
309
NSD001 Nose Disease 48 0.031
310
CRN017 Coronary Thrombosis 48 0.031
311
SYN036 Syncope 47 0.031
312
NLS001 Nelson Syndrome 47 0.031
313
PRT082 Preterm Premature Rupture of the Membranes 46 0.031
314
c SVR056 Severe Hemophilia a 43 0.031
315
LCH009 Lichen Sclerosus 41 0.031
316
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.031
317
IDP074 Idiopathic Bronchiectasis 36 0.031
318
TYP027 Type 1 Diabetes Mellitus 10 27 0.031
319
BSL036 Basal Cell Nevus Syndrome 65 0.030
320
P MCR010 Microcephaly 58 0.030
321
PRP083 Porphyria, Acute Intermittent 54 0.030
322
P DBT005 Diabetes Insipidus 53 0.030
323
LPR001 Lepromatous Leprosy 50 0.030
324
HLL004 Hellp Syndrome 50 0.030
325
ACT049 Acute Disseminated Encephalomyelitis 49 0.030
326
RTN003 Retinal Ischemia 48 0.030
327
P GRN010 Granular Cell Tumor 47 0.030
328
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.030
329
CRD137 Cardiogenic Shock 46 0.030
330
P ANL018 Analbuminemia 44 0.030
331
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.030
332
DBT008 Diabetic Angiopathy 44 0.030
333
P ERY048 Erythrocytosis, Familial, 2 42 0.030
334
SYM002 Sympathetic Ophthalmia 40 0.030
335
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.030
336
GST029 Gastric Cardia Adenocarcinoma 39 0.030
337
c ACT004 Acute Diarrhea 39 0.030
338
OST115 Osteonecrosis of the Jaw 38 0.030
339
CPL005 Capillary Disease 36 0.030
340
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 34 0.030
341
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 30 0.030
342
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.030
343
c DYS033 Dysautonomia Like Disorder 16 0.030
344
PLY125 Polycythemia Vera, Somatic 63 0.028
345
LPT001 Leptospirosis 62 0.028
346
P THR003 Thoracic Aortic Aneurysm 57 0.028
347
P HYP083 Hypopituitarism 54 0.028
348
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.028
349
PST021 Postpartum Depression 49 0.028
350
c CNG411 Congenital Disorder of Glycosylation, Type in 49 0.028
351
URN003 Urinary Schistosomiasis 48 0.028
352
BRN056 Bronchopulmonary Dysplasia 48 0.028
353
GGR001 Geographic Tongue 46 0.028
354
ADN001 Adenosine Deaminase Deficiency 45 0.028
355
HYP085 Hypothalamic Disease 44 0.028
356
PRD004 Prediabetes Syndrome 43 0.028
357
NRR001 Neuroretinitis 42 0.028
358
BLR008 Bilirubin Metabolic Disorder 42 0.028
359
c ACQ012 Acquired Angioedema 39 0.028
360
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.028
361
MTC005 Mitochondrial Metabolism Disease 36 0.028
362
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.028
363
NSP003 Nasopharyngeal Disease 26 0.028
364
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 24 0.028
365
VSC009 Vascular Skin Disease 19 0.028
366
ATM013 Autoimmune Disease of Cardiovascular System 13 0.028
367
P DYS007 Dyskeratosis Congenita 63 0.027
368
P NRC002 Narcolepsy 62 0.027
369
TKY002 Takayasu Arteritis 61 0.027
370
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 57 0.027
371
GLL022 Guillain-Barre Syndrome 56 0.027
372
c MYT020 Myotonic Dystrophy 2 56 0.027
373
PLS006 Plasmodium Vivax Malaria 53 0.027
374
ACH005 Achalasia 52 0.027
375
P DRM007 Dermatitis Herpetiformis 51 0.027
376
ATR002 Atransferrinemia 48 0.027
377
FML089 Familial Thoracic Aortic Aneurysm and Dissection 46 0.027
378
TBR006 Tuberculoid Leprosy 43 0.027
379
P SLL003 Salla Disease 43 0.027
380
ACT087 Acth Deficiency 43 0.027
381
SYN031 Synovial Chondromatosis 42 0.027
382
ESN002 Eosinophilia-Myalgia Syndrome 42 0.027
383
MRB001 Marburg Hemorrhagic Fever 41 0.027
384
PHM001 Phimosis 37 0.027
385
FNC002 Functional Diarrhea 37 0.027
386
FLC001 Folic Acid Deficiency Anemia 34 0.027
387
MLN003 Melancholia 34 0.027
388
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 0.027
389
MDY006 Mody, Type Iv 30 0.027
390
c AML016 Amelogenesis Imperfecta, Type 1e 30 0.027
391
IMM070 Immunodeficiency 13 27 0.027
392
LGD001 Leg Dermatosis 16 0.027
393
ORL014 Oral Pharyngeal Disorders 11 0.027
394
P CRG003 Crigler-Najjar Syndrome, Type I 59 0.025
395
LYS001 Loeys-Dietz Syndrome 58 0.025
396
P AVS004 Avascular Necrosis of the Femoral Head 56 0.025
397
P EXP004 Exophthalmos 53 0.025
398
c PRM012 Primary Polycythemia 52 0.025
399
RHM028 Rheumatic Heart Disease 50 0.025
400
WHP001 Whipple Disease 49 0.025
401
TWN001 Twin-to-Twin Transfusion Syndrome 48 0.025
402
MCR191 Microscopic Colitis 47 0.025
403
PST095 Post-Thrombotic Syndrome 47 0.025
404
ALB002 Albinism 46 0.025
405
IDP024 Idiopathic Inflammatory Myopathy 46 0.025
406
PNT038 Peanut Allergy 44 0.025
407
PRM020 Premenstrual Tension 44 0.025
408
BMF001 Bamforth-Lazarus Syndrome 42 0.025
409
MCR017 Macrocytic Anemia 42 0.025
410
RCR004 Recurrent Respiratory Papillomatosis 42 0.025
411
PRC003 Proctitis 41 0.025
412
DNT001 Dental Fluorosis 41 0.025
413
FTL021 Fetal Macrosomia 41 0.025
414
c CHR546 Chronic Mountain Sickness 40 0.025
415
DYS015 Dysentery 40 0.025
416
PRX034 Peroxisome Disorders 39 0.025
417
PRL019 Prolidase Deficiency 38 0.025
418
CYC007 Cyclic Thrombocytopenia 37 0.025
419
PNL013 Penile Disease 34 0.025
420
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 34 0.025
421
SPN185 Spinal Cord Infarction 34 0.025
422
FNT004 Fainting 33 0.025
423
ACT056 Acute Cor Pulmonale 33 0.025
424
GGN002 Gigantism 32 0.025
425
LVD002 Livedoid Vasculopathy 32 0.025
426
TMT002 Temtamy Preaxial Brachydactyly Syndrome 27 0.025
427
c DMN028 Diamond-Blackfan Anemia 12 27 0.025
428
KTT001 Ketothiolase Deficiency 24 0.025
429
SBC016 Subacute Delirium 24 0.025
430
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 23 0.025
431
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 22 0.025
432
ULC005 Ulcer of Lower Limbs 20 0.025
433
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 14 0.025
434
HMG024 Hemoglobinopathy Toms River 5 0.025
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