Search results for "hemoglobin c - beta-thalassemia"

The MalaCard for "hemoglobin c - beta-thalassemia" has been retired.
Searching MalaCards for entries containing "hemoglobin c - beta-thalassemia"

396 hits were found for 'hemoglobin c - beta-thalassemia'

# Family MCID Name MIFTS Score
1
c HMG001 Hemoglobin C Disease 47 6.211
2
SCK003 Sickle Cell Anemia 68 3.030
3
c VRL010 Viral Hepatitis 61 0.214
4
P BRS047 Breast Cancer 100 0.181
5
NRN002 Neuronitis 42 0.155
6
HMG012 Hemoglobin Constant Spring 19 0.148
7
PRS047 Prostatitis 56 0.144
8
HV1006 Hiv-1 82 0.143
9
P PRS040 Prostate Cancer 89 0.136
10
P MYC007 Myocardial Infarction 79 0.134
11
P NRB001 Neuroblastoma 69 0.130
12
P LNG032 Lung Cancer 94 0.124
13
HMG025 Hemoglobin H Disease, Nondeletional 37 0.119
14
CSY001 C Syndrome 49 0.118
15
ATH003 Atherosclerosis 62 0.117
16
RTN023 Retinitis 49 0.117
17
P OBS005 Obesity 93 0.116
18
P CLR023 Colorectal Cancer 97 0.116
19
HYP266 Hypoxia 55 0.115
20
P ADN016 Adenocarcinoma 69 0.113
21
ART111 Artery Disease 57 0.112
22
P CRN211 Coronary Artery Disease 75 0.111
23
GST053 Gastric Cancer 77 0.106
24
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.103
25
P HYP607 Hypercholesterolemia, Familial 77 0.102
26
c ACT075 Acute Myocardial Infarction 60 0.099
27
PRT036 Peritonitis 62 0.096
28
P RNL014 Renal Cell Carcinoma 81 0.094
29
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.093
30
P ESP024 Esophagitis 62 0.093
31
HMN014 Human Immunodeficiency Virus Infectious Disease 49 0.092
32
GLC008 Glucose Metabolism Disease 47 0.089
33
P CRV039 Cervicitis 44 0.087
34
HMG009 Hemoglobin Zurich 16 0.086
35
P MTH007 Methemoglobinemia 45 0.086
36
IMP003 Impaired Renal Function Disease 37 0.085
37
LPD008 Lipid Metabolism Disorder 58 0.085
38
P HMG016 Hemoglobin Sd 20 0.084
39
c HMG029 Hemoglobin Se Disease 27 0.083
40
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 26 0.083
41
MDY003 Mody, Type Ii 38 0.083
42
TBR010 Tuberculosis 69 0.082
43
P NRP001 Neuropathy 60 0.081
44
GST033 Gestational Diabetes 56 0.081
45
VSC007 Vascular Disease 67 0.080
46
P OVR042 Ovarian Cancer 75 0.080
47
P GLB002 Glioblastoma 66 0.080
48
P URF003 Urofacial Syndrome 1 52 0.079
49
HYP066 Hyperglycemia 60 0.078
50
URN009 Urinary System Disease 53 0.076
51
SRC014 Sarcoma 66 0.075
52
P AST005 Asthma 82 0.075
53
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.074
54
PRP027 Peripheral Vascular Disease 69 0.072
55
HYP056 Hypoglycemia 61 0.071
56
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 24 0.071
57
ISC006 Ischemic Heart Disease 68 0.071
58
DMN002 Dementia 64 0.070
59
SXL003 Sexual Disorder 47 0.070
60
P PLY018 Polycythemia 57 0.069
61
HMG002 Hemoglobinuria 49 0.069
62
P MLT019 Multiple Myeloma 80 0.067
63
ANG054 Angina Pectoris 51 0.067
64
P MCR129 Microvascular Complications of Diabetes 1 57 0.067
65
c PND001 Pain Disorder 55 0.067
66
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.067
67
ADL002 Adult Syndrome 53 0.066
68
P PLY011 Polycystic Ovary Syndrome 66 0.066
69
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.065
70
P NTR004 Neutropenia 59 0.065
71
PRD007 Periodontal Disease 43 0.064
72
P LYM026 Lymphoblastic Leukemia 60 0.064
73
P DRR001 Diarrhea 51 0.064
74
IMM071 Immunodeficiency 12 28 0.063
75
PLM033 Pulmonary Embolism 59 0.063
76
TRN018 Transitional Cell Carcinoma 54 0.063
77
PRT014 Protein S Deficiency 52 0.062
78
STR067 Stroke, Ischemic 77 0.062
79
P NSP012 Nasopharyngeal Carcinoma 67 0.062
80
P HYP060 Hyperinsulinism 59 0.062
81
PLS007 Plasmodium Falciparum Malaria 54 0.061
82
c CHR090 Chronic Lymphocytic Leukemia 74 0.061
83
CLT003 Colitis 59 0.060
84
GLC003 Glucose Intolerance 55 0.060
85
LNG099 Lung Disease 62 0.060
86
P EXN002 Exanthem 57 0.060
87
P HYP086 Hypothyroidism 65 0.059
88
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.059
89
IMM076 Immunodeficiency 24 27 0.059
90
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.059
91
VTM003 Vitamin Metabolic Disorder 33 0.059
92
GLC006 Galactosemia 67 0.058
93
BRN004 Brain Edema 51 0.058
94
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.058
95
ATM052 Autoimmune Disease 1 28 0.058
96
CHR005 Chorioamnionitis 48 0.057
97
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.057
98
c CRN174 Coronary Heart Disease 2 22 0.056
99
HDN004 Head and Neck Carcinoma 55 0.056
100
P GT001 Gout 58 0.056
101
ORL011 Oral Cancer 55 0.055
102
PHR003 Pharyngitis 58 0.055
103
HPT074 Hepatic Adenoma, Somatic 51 0.055
104
HNM002 Hinman Syndrome 25 0.055
105
ATM053 Autoimmune Disease 2 19 0.055
106
P END044 Endometriosis 53 0.055
107
P PLM036 Pulmonary Fibrosis 68 0.055
108
ANM029 Anemia, Sideroblastic, X-Linked 49 0.055
109
c THR092 Thrombophilia Due to Thrombin Defect 56 0.054
110
P ESS003 Essential Thrombocythemia 68 0.054
111
c TRC078 Trichohepatoenteric Syndrome 2 31 0.054
112
P FML035 Familial Hyperlipidemia 50 0.053
113
P ALC004 Alcohol Abuse 60 0.053
114
LRN003 Learning Disability 51 0.053
115
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 53 0.053
116
HYD038 Hydrops Fetalis, Nonimmune 40 0.053
117
PLC008 Placenta Disease 36 0.053
118
P CLR108 Colorectal Adenoma 60 0.052
119
P HYP069 Hyperparathyroidism 57 0.052
120
ATM014 Autoimmune Disease of Endocrine System 37 0.052
121
P CNJ013 Conjunctivitis 65 0.052
122
SPN051 Spondylitis 50 0.052
123
P ECL001 Eclampsia 54 0.051
124
CYN002 Cyanosis, Transient Neonatal 31 0.051
125
P ENC004 Encephalitis 61 0.051
126
SKN023 Skin Tag 46 0.051
127
MSC004 Muscle Tissue Disease 36 0.050
128
OST017 Osteomyelitis 59 0.050
129
c MYC058 Myocardial Infarction 2 29 0.050
130
VSC006 Vascular Cancer 54 0.050
131
LYM019 Lymphosarcoma 53 0.050
132
P SYP003 Syphilis 53 0.049
133
RFR010 Refractory Anemia 45 0.049
134
P PLY019 Polyneuropathy 54 0.049
135
BRN071 Brain Injury 52 0.049
136
SYS003 Systolic Heart Failure 43 0.048
137
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 29 0.048
138
HPY002 H. Pylori Infection 58 0.048
139
P GST044 Gastritis 58 0.048
140
TXC005 Toxic Shock Syndrome 61 0.047
141
P MYL005 Myelofibrosis 67 0.047
142
CHL067 Cholecystitis 56 0.047
143
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.047
144
CHR008 Choroiditis 43 0.047
145
c CNG119 Congenital Porphyria 23 0.047
146
P SDD001 Sudden Infant Death Syndrome 61 0.047
147
INT002 Intermittent Claudication 56 0.047
148
ADP007 Adie Pupil 34 0.047
149
P HYP117 Hypertriglyceridemia 65 0.047
150
RSP006 Respiratory System Disease 62 0.047
151
ATN002 Autonomic Nervous System Disease 47 0.046
152
P DMY001 Demyelinating Polyneuropathy 43 0.046
153
PLS009 Plasma Cell Neoplasm 48 0.046
154
c ADL001 Adult Lymphoma 41 0.046
155
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.046
156
GNG011 Gingival Disease 51 0.046
157
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 45 0.046
158
P NRV006 Nervous System Cancer 62 0.046
159
BRN106 Burns 52 0.046
160
BRN080 Brain Ischemia 41 0.046
161
LMB062 Limb Ischemia 48 0.045
162
P RTN014 Retinal Artery Occlusion 43 0.045
163
ATM012 Autoimmune Disease of Blood 37 0.045
164
ACD009 Acid-Labile Subunit, Deficiency of 48 0.045
165
c THR037 Thrombocytopenia 2 37 0.045
166
INS001 Insulinoma 59 0.045
167
DBT010 Diabetic Neuropathy 55 0.045
168
CRB025 Carbohydrate Metabolic Disorder 47 0.045
169
ATM055 Autoimmune Disease 4 18 0.045
170
SCH014 Schistosomiasis 58 0.044
171
BCL002 B Cell Deficiency 50 0.044
172
BNF002 Bone Fracture 47 0.044
173
P SKN013 Skin Benign Neoplasm 46 0.044
174
GRN017 Granulocytopenia 42 0.044
175
HNZ001 Heinz Body Anemia 38 0.044
176
P RSP003 Respiratory Failure 70 0.044
177
LSH001 Leishmaniasis 62 0.044
178
P CRT072 Creutzfeldt-Jakob Disease 63 0.044
179
APH001 Aphthous Stomatitis 62 0.044
180
MLT021 Multiple System Atrophy 71 0.043
181
RDN001 Reading Disorder 39 0.043
182
P BPL003 Bipolar Disorder 62 0.043
183
PPL022 Papilloma 55 0.043
184
ATR060 Atrial Standstill, Digenic 53 0.043
185
KWS001 Kwashiorkor 44 0.043
186
ANM001 Anemia of Prematurity 43 0.043
187
P LPR003 Leprosy 68 0.042
188
ALC007 Alcohol Dependence 65 0.042
189
P LCT001 Lactic Acidosis 52 0.042
190
c DRR009 Diarrhea 6 31 0.042
191
BRC012 Brucellosis 65 0.041
192
c BSL007 Basal Cell Carcinoma 64 0.041
193
BRS051 Breast Disease 62 0.041
194
SPT004 Septic Arthritis 59 0.041
195
STM007 Stomatitis 50 0.041
196
FML039 Female Reproductive System Disease 48 0.041
197
CRT015 Carotid Artery Occlusion 43 0.041
198
KRT002 Keratomalacia 54 0.041
199
c CHR418 Chronic Leukemia 48 0.041
200
CRB004 Cerebral Artery Occlusion 46 0.041
201
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.040
202
SHW002 Shwachman-Diamond Syndrome 60 0.040
203
P PYL005 Pyelonephritis 52 0.040
204
CRT049 Critical Limb Ischemia 51 0.040
205
RHM001 Rheumatic Fever 50 0.040
206
c HYP595 Hypertension, Essential 69 0.040
207
RNL101 Renal Cell Carcinoma, Papillary 67 0.040
208
c THR048 Thrombocytopenia 4 29 0.040
209
TTH006 Tooth Disease 52 0.039
210
c ACT071 Acute Kidney Failure 50 0.039
211
PRP021 Peripheral Nervous System Neoplasm 50 0.039
212
MXD023 Mixed Cell Type Cancer 47 0.039
213
CRB085 Cerebral Hemorrhage 43 0.039
214
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 21 0.039
215
P THY097 Thyroid Hormone Resistance 54 0.039
216
TRM010 Traumatic Brain Injury 52 0.039
217
FRB001 Farber Lipogranulomatosis 51 0.039
218
SNS023 Sensory System Cancer 46 0.039
219
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 29 0.039
220
MND006 Mondor Disease 21 0.039
221
c ACT042 Acute Pyelonephritis 46 0.038
222
c CNT028 Central Retinal Artery Occlusion 35 0.038
223
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 24 0.038
224
CRV047 Cervical Cancer, Somatic 65 0.038
225
CHL069 Cholesteatoma 51 0.038
226
TRN015 Transient Cerebral Ischemia 56 0.037
227
P INT063 Intellectual Disability 53 0.037
228
CRV040 Cervix Carcinoma 53 0.037
229
HML006 Hemolytic Anemia Due to G6pd Deficiency 35 0.037
230
DBT062 Diabetic Foot Ulcers 52 0.036
231
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 23 0.036
232
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 19 0.036
233
ANR002 Aniridia 60 0.036
234
GTR002 Goiter 54 0.036
235
THY030 Thyroid Gland Disease 51 0.036
236
CRN030 Coronary Stenosis 50 0.036
237
URM002 Uremia 50 0.036
238
P EPD002 Epidermolytic Hyperkeratosis 49 0.036
239
P PCH015 Pachyonychia Congenita 1 49 0.036
240
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.036
241
ATN005 Autonomic Dysfunction 45 0.036
242
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.035
243
P SHR029 Short Syndrome 60 0.035
244
P SZR006 Seizure Disorder 57 0.035
245
INT007 Intermediate Coronary Syndrome 52 0.035
246
FML038 Female Reproductive Organ Cancer 51 0.035
247
GRW007 Growth Hormone Deficiency 48 0.035
248
P ATR005 Atrophic Gastritis 45 0.035
249
MDY005 Mody, Type I 33 0.035
250
CRZ001 Crouzon Syndrome 70 0.034
251
P HMR012 Hemorrhagic Fever 55 0.034
252
ORL004 Oral Submucous Fibrosis 51 0.034
253
CRN017 Coronary Thrombosis 48 0.034
254
SDD007 Sudden Cardiac Death 46 0.034
255
c GRV008 Graves Disease 1 45 0.034
256
AYM001 Ayme-Gripp Syndrome 45 0.034
257
LYM067 Lymphoid Leukemia 43 0.034
258
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 39 0.034
259
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.034
260
ALX002 Alexithymia 37 0.034
261
KTT001 Ketothiolase Deficiency 25 0.034
262
CLR065 Colorectal Adenomatous Polyposis, Autosomal Recessive, with Pilomatricomas 46 0.034
263
GLC009 Glucosephosphate Dehydrogenase Deficiency 40 0.034
264
P MRC003 Mercury Poisoning 38 0.034
265
ANM030 Anemia, Hypochromic Microcytic 37 0.034
266
c DMN006 Diamond-Blackfan Anemia 3 30 0.034
267
c DYS168 Dyserythropoietic Anemia, Congenital, Type Iv 25 0.034
268
P CWD006 Cowden Syndrome 1 68 0.033
269
VSC003 Visceral Leishmaniasis 55 0.033
270
P MTC069 Mitochondrial Disorders 52 0.033
271
PRT038 Protein-Energy Malnutrition 49 0.033
272
P TRC086 Trichohepatoenteric Syndrome 1 46 0.033
273
EPD065 Epidermolytic Ichthyosis 35 0.033
274
CRV069 Cervix Disease 34 0.033
275
c AST037 Asthma 1 31 0.033
276
MNT045 Montefiore Syndrome 13 0.033
277
P CLC005 Celiac Disease 67 0.032
278
P RCK004 Rickets 59 0.032
279
GLS001 Gliosarcoma 55 0.032
280
VSC002 Vascular Dementia 54 0.032
281
NSD001 Nose Disease 52 0.032
282
FML037 Female Breast Cancer 51 0.032
283
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.032
284
HLL004 Hellp Syndrome 49 0.032
285
SYN036 Syncope 47 0.032
286
PRT082 Preterm Premature Rupture of the Membranes 47 0.032
287
EPD047 Epidermolysis Bullosa Simplex, Koebner Type 42 0.032
288
c GLL024 Gallbladder Disease 1 38 0.032
289
P ATX010 Ataxia Neuropathy Spectrum 28 0.032
290
c LKM004 Leukemia, B-Cell, Chronic 25 0.032
291
EPD036 Epidermolysis Bullosa Simplex, Other Generalized 20 0.032
292
P MCR010 Microcephaly 58 0.031
293
PRP083 Porphyria, Acute Intermittent 55 0.031
294
P STR020 Strabismus 53 0.031
295
KRT009 Keratosis 50 0.031
296
LPR001 Lepromatous Leprosy 49 0.031
297
RTN003 Retinal Ischemia 48 0.031
298
RSP002 Respiratory Syncytial Virus Infectious Disease 48 0.031
299
PLM102 Palmoplantar Keratoderma, Epidermolytic 48 0.031
300
CRD137 Cardiogenic Shock 46 0.031
301
P ANL018 Analbuminemia 46 0.031
302
DBT008 Diabetic Angiopathy 45 0.031
303
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.031
304
CPL005 Capillary Disease 40 0.031
305
c ACT004 Acute Diarrhea 38 0.031
306
OST032 Osteofibrous Dysplasia 38 0.031
307
PRS127 Pearson Marrow-Pancreas Syndrome 34 0.031
308
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 26 0.031
309
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 23 0.031
310
PLY125 Polycythemia Vera, Somatic 63 0.029
311
DNG002 Dengue Hemorrhagic Fever 62 0.029
312
ACH005 Achalasia 54 0.029
313
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.029
314
BRN056 Bronchopulmonary Dysplasia 49 0.029
315
URN003 Urinary Schistosomiasis 47 0.029
316
P GRN010 Granular Cell Tumor 47 0.029
317
DCB001 Decubitus Ulcer 44 0.029
318
EPD028 Epidermolysis Bullosa Simplex, Dowling-Meara Type 44 0.029
319
ICH002 Ichthyosis Bullosa of Siemens 43 0.029
320
PRD004 Prediabetes Syndrome 43 0.029
321
NRR001 Neuroretinitis 42 0.029
322
MTC005 Mitochondrial Metabolism Disease 38 0.029
323
VTM001 Vitamin K Deficiency Hemorrhagic Disease 36 0.029
324
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.029
325
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.029
326
NSP003 Nasopharyngeal Disease 30 0.029
327
PLM135 Palmoplantar Keratoderma, Bothnian Type 29 0.029
328
HRN022 Hearing Loss/deafness 25 0.029
329
VSC009 Vascular Skin Disease 22 0.029
330
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 19 0.029
331
ATM013 Autoimmune Disease of Cardiovascular System 15 0.029
332
P DYS007 Dyskeratosis Congenita 63 0.028
333
P EPD003 Epidermolysis Bullosa Simplex 51 0.028
334
AML029 Ameloblastoma 46 0.028
335
ADN001 Adenosine Deaminase Deficiency 45 0.028
336
ESN011 Eisenmenger Syndrome 44 0.028
337
P SLL003 Salla Disease 43 0.028
338
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.028
339
c CHR546 Chronic Mountain Sickness 42 0.028
340
FTL021 Fetal Macrosomia 41 0.028
341
BSL006 Basaloid Squamous Cell Carcinoma 41 0.028
342
CHR034 Chromophobe Adenoma 41 0.028
343
GST028 Gastric Squamous Cell Carcinoma 39 0.028
344
FNC002 Functional Diarrhea 38 0.028
345
CYC007 Cyclic Thrombocytopenia 37 0.028
346
PHM001 Phimosis 37 0.028
347
SPN185 Spinal Cord Infarction 36 0.028
348
FRN014 Fournier Gangrene 34 0.028
349
FNT004 Fainting 33 0.028
350
MDY006 Mody, Type Iv 33 0.028
351
ACT056 Acute Cor Pulmonale 31 0.028
352
IMM070 Immunodeficiency 13 29 0.028
353
HYP029 Hyperthyroxinemia 25 0.028
354
ORL014 Oral Pharyngeal Disorders 14 0.028
355
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 58 0.026
356
P AVS004 Avascular Necrosis of the Femoral Head 56 0.026
357
P EXP004 Exophthalmos 54 0.026
358
CRN036 Craniopharyngioma 52 0.026
359
PLC005 Placental Insufficiency 50 0.026
360
PST095 Post-Thrombotic Syndrome 50 0.026
361
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 46 0.026
362
TWN001 Twin-to-Twin Transfusion Syndrome 46 0.026
363
VLV044 Vulvar Intraepithelial Neoplasia 46 0.026
364
PRS036 Parasitic Protozoa Infectious Disease 45 0.026
365
P ICH001 Ichthyosis Vulgaris 44 0.026
366
PRC003 Proctitis 43 0.026
367
ALB002 Albinism 43 0.026
368
P ERY048 Erythrocytosis, Familial, 2 42 0.026
369
CHR100 Chronic Ulcer of Skin 42 0.026
370
STT007 Steatocystoma Multiplex 42 0.026
371
MCR017 Macrocytic Anemia 41 0.026
372
DYS015 Dysentery 41 0.026
373
EPD041 Epidermolysis Bullosa Simplex, Weber-Cockayne Type 41 0.026
374
PRX034 Peroxisome Disorders 40 0.026
375
MRS001 Marasmus 39 0.026
376
PRL019 Prolidase Deficiency 38 0.026
377
ETH004 Euthyroid Sick Syndrome 38 0.026
378
BRS063 Breast Squamous Cell Carcinoma 37 0.026
379
OSG001 Osgood-Schlatter's Disease 36 0.026
380
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 35 0.026
381
ODN006 Odontoma 34 0.026
382
PNC019 Pancreatoblastoma 32 0.026
383
c DFN280 Deafness, Autosomal Recessive 31 0.026
384
c MLG080 Malignant Secondary Hypertension 30 0.026
385
c EPD058 Epidermolysis Bullosa Simplex, Recessive 1 29 0.026
386
SBC016 Subacute Delirium 27 0.026
387
c DMN028 Diamond-Blackfan Anemia 12 27 0.026
388
GGN002 Gigantism 27 0.026
389
TXC004 Toxic Diffuse Goiter 27 0.026
390
ICH036 Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis 24 0.026
391
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 23 0.026
392
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 23 0.026
393
ULC005 Ulcer of Lower Limbs 22 0.026
394
P DYS070 Dysalbuminemic Hyperthyroxinemia 20 0.026
395
LGD001 Leg Dermatosis 19 0.026
396
PRM123 Paramyloidosis 16 0.026