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"

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

# Family MCID Name MIFTS Score
1
c HMG001 Hemoglobin C Disease 47 6.222
2
SCK003 Sickle Cell Anemia 71 3.039
3
c VRL010 Viral Hepatitis 60 0.228
4
P BRS047 Breast Cancer 100 0.184
5
NRN002 Neuronitis 41 0.156
6
PRS047 Prostatitis 56 0.145
7
HMG012 Hemoglobin Constant Spring 18 0.142
8
P PRS040 Prostate Cancer 90 0.136
9
P MYC007 Myocardial Infarction 79 0.135
10
P NRB001 Neuroblastoma 70 0.132
11
P LNG032 Lung Cancer 95 0.128
12
P CLR023 Colorectal Cancer 97 0.120
13
CSY001 C Syndrome 50 0.119
14
HV1006 Hiv-1 80 0.118
15
SQM006 Squamous Cell Carcinoma 70 0.118
16
GST053 Gastric Cancer 78 0.117
17
ATH003 Atherosclerosis 65 0.117
18
P OBS005 Obesity 92 0.117
19
RTN023 Retinitis 50 0.117
20
MLN008 Melanoma 62 0.116
21
P ADN016 Adenocarcinoma 69 0.115
22
c HPT015 Hepatitis D 52 0.114
23
HYP266 Hypoxia 56 0.114
24
ART111 Artery Disease 55 0.112
25
P CRN211 Coronary Artery Disease 74 0.111
26
P HYP607 Hypercholesterolemia, Familial 76 0.107
27
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.104
28
c ACT075 Acute Myocardial Infarction 60 0.098
29
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.097
30
PRT036 Peritonitis 63 0.096
31
P RNL014 Renal Cell Carcinoma 82 0.095
32
ACQ007 Acquired Immunodeficiency Syndrome 60 0.095
33
P ESP024 Esophagitis 61 0.095
34
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.093
35
GLC008 Glucose Metabolism Disease 42 0.091
36
HMG009 Hemoglobin Zurich 16 0.088
37
P CRV039 Cervicitis 45 0.088
38
P MTH007 Methemoglobinemia 45 0.086
39
IMP003 Impaired Renal Function Disease 34 0.086
40
MDY003 Mody, Type Ii 36 0.085
41
LPD008 Lipid Metabolism Disorder 58 0.085
42
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.084
43
c HPT007 Hepatitis E 54 0.083
44
TBR010 Tuberculosis 70 0.082
45
P OVR042 Ovarian Cancer 76 0.081
46
P GLB002 Glioblastoma 68 0.081
47
P NRP001 Neuropathy 59 0.081
48
VSC007 Vascular Disease 67 0.079
49
GST033 Gestational Diabetes 57 0.079
50
c HMG029 Hemoglobin Se Disease 28 0.079
51
P MLT019 Multiple Myeloma 83 0.078
52
HYP066 Hyperglycemia 61 0.077
53
SRC014 Sarcoma 66 0.076
54
P AST005 Asthma 82 0.075
55
URN009 Urinary System Disease 50 0.075
56
P URF003 Urofacial Syndrome 1 50 0.074
57
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.074
58
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.072
59
PRP027 Peripheral Vascular Disease 69 0.070
60
DMN002 Dementia 65 0.070
61
HYP056 Hypoglycemia 61 0.070
62
ISC006 Ischemic Heart Disease 68 0.070
63
c CHR090 Chronic Lymphocytic Leukemia 76 0.069
64
P PLY018 Polycythemia 58 0.069
65
P INF037 Inflammatory Bowel Disease 63 0.068
66
SXL003 Sexual Disorder 42 0.068
67
HMG002 Hemoglobinuria 48 0.067
68
VSC011 Vasculitis 62 0.067
69
c PND001 Pain Disorder 54 0.067
70
ANG054 Angina Pectoris 50 0.066
71
P PLY011 Polycystic Ovary Syndrome 65 0.066
72
P MCR129 Microvascular Complications of Diabetes 1 54 0.065
73
P LYM026 Lymphoblastic Leukemia 62 0.065
74
P NTR004 Neutropenia 59 0.065
75
ADL002 Adult Syndrome 52 0.065
76
PLS007 Plasmodium Falciparum Malaria 55 0.064
77
IMM071 Immunodeficiency 12 26 0.064
78
P DRR001 Diarrhea 60 0.064
79
P NSP012 Nasopharyngeal Carcinoma 66 0.064
80
PRD007 Periodontal Disease 60 0.063
81
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.063
82
TRN018 Transitional Cell Carcinoma 53 0.063
83
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.062
84
PRT014 Protein S Deficiency 53 0.062
85
PLM033 Pulmonary Embolism 60 0.061
86
P HYP060 Hyperinsulinism 58 0.061
87
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.061
88
MRF001 Marfan Syndrome 73 0.061
89
P EXN002 Exanthem 57 0.060
90
CLT003 Colitis 60 0.060
91
LNG099 Lung Disease 64 0.060
92
IMM076 Immunodeficiency 24 27 0.060
93
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.060
94
GLC003 Glucose Intolerance 55 0.060
95
ANR040 Aneurysm 57 0.059
96
c CNT068 Central Pain Syndrome 29 0.059
97
VTM003 Vitamin Metabolic Disorder 30 0.059
98
c ATM011 Autoimmune Hepatitis 60 0.059
99
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 9 0.057
100
BRN004 Brain Edema 52 0.057
101
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.057
102
GLC006 Galactosemia 64 0.057
103
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.057
104
HPT074 Hepatic Adenoma, Somatic 50 0.057
105
HNM002 Hinman Syndrome 25 0.057
106
ATM052 Autoimmune Disease 1 25 0.057
107
CHR005 Chorioamnionitis 48 0.056
108
P PLM036 Pulmonary Fibrosis 71 0.056
109
PHR003 Pharyngitis 56 0.056
110
HYD038 Hydrops Fetalis, Nonimmune 40 0.055
111
STR067 Stroke, Ischemic 75 0.055
112
c CRN174 Coronary Heart Disease 2 20 0.055
113
P ALC004 Alcohol Abuse 59 0.055
114
P END044 Endometriosis 66 0.055
115
P GT001 Gout 58 0.055
116
P ESS003 Essential Thrombocythemia 70 0.055
117
c TRC078 Trichohepatoenteric Syndrome 2 29 0.054
118
ATM053 Autoimmune Disease 2 16 0.054
119
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.053
120
P FML035 Familial Hyperlipidemia 48 0.053
121
c THR092 Thrombophilia Due to Thrombin Defect 54 0.052
122
SCH014 Schistosomiasis 58 0.052
123
SPN051 Spondylitis 51 0.052
124
LRN003 Learning Disability 49 0.052
125
P CLR108 Colorectal Adenoma 60 0.052
126
c PRC016 Pre-Eclampsia 56 0.052
127
P HYP069 Hyperparathyroidism 58 0.052
128
PLC008 Placenta Disease 33 0.052
129
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 51 0.051
130
P CNJ013 Conjunctivitis 64 0.051
131
P DBT083 Diabetes Mellitus, Permanent Neonatal 55 0.051
132
MSC004 Muscle Tissue Disease 34 0.051
133
P ENC004 Encephalitis 63 0.051
134
P ECL001 Eclampsia 54 0.051
135
ATM014 Autoimmune Disease of Endocrine System 36 0.051
136
P HYP086 Hypothyroidism 64 0.050
137
SKN023 Skin Tag 44 0.050
138
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.050
139
VSC006 Vascular Cancer 51 0.050
140
P SYP003 Syphilis 53 0.050
141
LYM019 Lymphosarcoma 53 0.050
142
CYN002 Cyanosis, Transient Neonatal 28 0.049
143
OST017 Osteomyelitis 61 0.049
144
c MYC058 Myocardial Infarction 2 28 0.049
145
BRN071 Brain Injury 52 0.049
146
P PLY019 Polyneuropathy 56 0.049
147
RFR010 Refractory Anemia 45 0.048
148
ART016 Aortic Aneurysm 69 0.048
149
P PLY014 Polycystic Kidney Disease 53 0.048
150
P MYL005 Myelofibrosis 67 0.048
151
SYS003 Systolic Heart Failure 43 0.048
152
HPY002 H. Pylori Infection 61 0.048
153
P GST044 Gastritis 56 0.048
154
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 43 0.047
155
TXC005 Toxic Shock Syndrome 60 0.047
156
PLS009 Plasma Cell Neoplasm 48 0.047
157
P NRV006 Nervous System Cancer 60 0.046
158
CHL067 Cholecystitis 57 0.046
159
CHR008 Choroiditis 44 0.046
160
P HYP117 Hypertriglyceridemia 61 0.046
161
RSP006 Respiratory System Disease 58 0.046
162
BRN080 Brain Ischemia 41 0.046
163
INT002 Intermittent Claudication 56 0.046
164
LMB062 Limb Ischemia 48 0.045
165
ACD009 Acid-Labile Subunit, Deficiency of 45 0.045
166
BNF002 Bone Fracture 50 0.045
167
BCL002 B Cell Deficiency 49 0.045
168
c ADL001 Adult Lymphoma 39 0.045
169
ATN002 Autonomic Nervous System Disease 48 0.045
170
ATM012 Autoimmune Disease of Blood 35 0.045
171
ATM055 Autoimmune Disease 4 15 0.045
172
GNG011 Gingival Disease 46 0.045
173
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.044
174
GRN017 Granulocytopenia 44 0.044
175
c THR037 Thrombocytopenia 2 35 0.044
176
P CRT072 Creutzfeldt-Jakob Disease 61 0.044
177
INS001 Insulinoma 61 0.044
178
DBT010 Diabetic Neuropathy 55 0.044
179
ATN005 Autonomic Dysfunction 49 0.044
180
CRB025 Carbohydrate Metabolic Disorder 46 0.044
181
P RTN014 Retinal Artery Occlusion 44 0.044
182
ADP007 Adie Pupil 34 0.044
183
MDY005 Mody, Type I 30 0.044
184
LSH001 Leishmaniasis 66 0.044
185
NSY001 N Syndrome 36 0.044
186
P SDD001 Sudden Infant Death Syndrome 61 0.043
187
HNZ001 Heinz Body Anemia 39 0.043
188
P RSP003 Respiratory Failure 71 0.043
189
MLT021 Multiple System Atrophy 70 0.043
190
RNL101 Renal Cell Carcinoma, Papillary 63 0.043
191
SLP005 Sleep Disorder 53 0.043
192
RDN001 Reading Disorder 34 0.043
193
APH001 Aphthous Stomatitis 62 0.043
194
ATR060 Atrial Standstill, Digenic 51 0.043
195
P LPR003 Leprosy 69 0.042
196
P BPL003 Bipolar Disorder 62 0.042
197
c TYP024 Type Ii Mixed Cryoglobulinemia 33 0.042
198
P HMR012 Hemorrhagic Fever 56 0.042
199
ALC007 Alcohol Dependence 63 0.042
200
P LCT001 Lactic Acidosis 51 0.042
201
c CHR418 Chronic Leukemia 47 0.042
202
ANM001 Anemia of Prematurity 41 0.041
203
BRC012 Brucellosis 66 0.041
204
CRV047 Cervical Cancer, Somatic 65 0.041
205
SPT004 Septic Arthritis 60 0.041
206
KRT002 Keratomalacia 52 0.041
207
STM007 Stomatitis 50 0.041
208
FML039 Female Reproductive System Disease 48 0.041
209
AYM001 Ayme-Gripp Syndrome 41 0.041
210
c DRR009 Diarrhea 6 29 0.041
211
BRS051 Breast Disease 61 0.040
212
c ACT071 Acute Kidney Failure 49 0.040
213
HYP099 Hyperferritinemia-Cataract Syndrome 42 0.040
214
c HYP595 Hypertension, Essential 69 0.040
215
MYL031 Myeloproliferative Neoplasm 58 0.040
216
VGT001 Vogt-Koyanagi-Harada Disease 55 0.040
217
TTH006 Tooth Disease 52 0.040
218
KLD001 Keloids 51 0.040
219
P AGG001 Aggressive Periodontitis 50 0.040
220
c CNG415 Congenital Disorder of Glycosylation, Type Ia 45 0.040
221
CRB004 Cerebral Artery Occlusion 45 0.040
222
CRT015 Carotid Artery Occlusion 43 0.040
223
c THR048 Thrombocytopenia 4 27 0.040
224
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.040
225
P CLC005 Celiac Disease 68 0.040
226
SHW002 Shwachman-Diamond Syndrome 61 0.040
227
RHM001 Rheumatic Fever 54 0.040
228
P PYL005 Pyelonephritis 52 0.040
229
CRT049 Critical Limb Ischemia 51 0.040
230
SHH001 Sheehan Syndrome 44 0.039
231
TRM010 Traumatic Brain Injury 52 0.039
232
CRB085 Cerebral Hemorrhage 46 0.039
233
PRP021 Peripheral Nervous System Neoplasm 46 0.039
234
MXD023 Mixed Cell Type Cancer 45 0.039
235
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 25 0.038
236
SNS023 Sensory System Cancer 43 0.038
237
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.038
238
MND006 Mondor Disease 21 0.038
239
FRB001 Farber Lipogranulomatosis 53 0.037
240
HYP457 Hypertrophic Scars 45 0.037
241
DNG002 Dengue Hemorrhagic Fever 63 0.037
242
DBT062 Diabetic Foot Ulcers 51 0.037
243
c ACT042 Acute Pyelonephritis 45 0.037
244
c CNT028 Central Retinal Artery Occlusion 37 0.037
245
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 36 0.037
246
FRN014 Fournier Gangrene 35 0.037
247
CRZ001 Crouzon Syndrome 70 0.037
248
BLL006 Bullous Pemphigoid 59 0.037
249
P RBL001 Rubella 57 0.037
250
TRN015 Transient Cerebral Ischemia 56 0.037
251
CRV040 Cervix Carcinoma 53 0.037
252
P DMY001 Demyelinating Polyneuropathy 43 0.037
253
HML006 Hemolytic Anemia Due to G6pd Deficiency 33 0.037
254
P ANR002 Aniridia 64 0.036
255
ESP020 Esophageal Atresia 50 0.036
256
URM002 Uremia 48 0.036
257
P TRC086 Trichohepatoenteric Syndrome 1 48 0.036
258
LYM067 Lymphoid Leukemia 44 0.036
259
P THR027 Thoracic Aortic Aneurysms and Aortic Dissections 43 0.036
260
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.035
261
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 22 0.035
262
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.035
263
P SHR029 Short Syndrome 58 0.035
264
P END033 Endocarditis 54 0.035
265
CRN030 Coronary Stenosis 51 0.035
266
GRW007 Growth Hormone Deficiency 50 0.035
267
FML038 Female Reproductive Organ Cancer 50 0.035
268
P INT063 Intellectual Disability 49 0.035
269
P ATR005 Atrophic Gastritis 45 0.035
270
P DYS021 Dysautonomia 44 0.035
271
PTY001 Pityriasis Rosea 42 0.035
272
P CHL066 Cholangitis 42 0.035
273
ORL004 Oral Submucous Fibrosis 51 0.034
274
INT007 Intermediate Coronary Syndrome 50 0.034
275
SDD007 Sudden Cardiac Death 47 0.034
276
BLL004 Bullous Keratopathy 44 0.034
277
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 0.034
278
PRN049 Paraneoplastic Pemphigus 40 0.034
279
ALX002 Alexithymia 37 0.034
280
ATM015 Autoimmune Disease of Gastrointestinal Tract 34 0.034
281
c LKM004 Leukemia, B-Cell, Chronic 24 0.034
282
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.033
283
PRS036 Parasitic Protozoa Infectious Disease 41 0.033
284
ANM030 Anemia, Hypochromic Microcytic 36 0.033
285
c DMN006 Diamond-Blackfan Anemia 3 29 0.033
286
SPN331 Spondyloocular Syndrome 27 0.033
287
c DYS168 Dyserythropoietic Anemia, Congenital, Type Iv 25 0.033
288
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.033
289
P RCK004 Rickets 61 0.033
290
P SZR006 Seizure Disorder 56 0.033
291
VSC003 Visceral Leishmaniasis 56 0.033
292
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 55 0.033
293
P MTC069 Mitochondrial Disorders 53 0.033
294
CRV069 Cervix Disease 32 0.033
295
c AST037 Asthma 1 29 0.033
296
MNT045 Montefiore Syndrome 10 0.033
297
ART017 Aortic Disease 57 0.032
298
GLS001 Gliosarcoma 55 0.032
299
VSC002 Vascular Dementia 54 0.032
300
FML037 Female Breast Cancer 50 0.032
301
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.032
302
NSD001 Nose Disease 48 0.032
303
CRN017 Coronary Thrombosis 48 0.032
304
SYN036 Syncope 47 0.032
305
c CNG206 Congenital Disorder of Glycosylation, Type Ie 47 0.032
306
NLS001 Nelson Syndrome 47 0.032
307
PRT082 Preterm Premature Rupture of the Membranes 46 0.032
308
c SVR056 Severe Hemophilia a 43 0.032
309
LCH009 Lichen Sclerosus 41 0.032
310
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.032
311
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 38 0.032
312
IDP074 Idiopathic Bronchiectasis 36 0.032
313
TYP027 Type 1 Diabetes Mellitus 10 27 0.032
314
BSL036 Basal Cell Nevus Syndrome 65 0.030
315
P MCR010 Microcephaly 58 0.030
316
PRP083 Porphyria, Acute Intermittent 54 0.030
317
P DBT005 Diabetes Insipidus 53 0.030
318
LPR001 Lepromatous Leprosy 50 0.030
319
HLL004 Hellp Syndrome 50 0.030
320
ACT049 Acute Disseminated Encephalomyelitis 49 0.030
321
RTN003 Retinal Ischemia 48 0.030
322
P GRN010 Granular Cell Tumor 47 0.030
323
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.030
324
CRD137 Cardiogenic Shock 46 0.030
325
P ANL018 Analbuminemia 44 0.030
326
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.030
327
DBT008 Diabetic Angiopathy 44 0.030
328
P ERY048 Erythrocytosis, Familial, 2 42 0.030
329
SYM002 Sympathetic Ophthalmia 40 0.030
330
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.030
331
GST029 Gastric Cardia Adenocarcinoma 39 0.030
332
c ACT004 Acute Diarrhea 39 0.030
333
OST115 Osteonecrosis of the Jaw 38 0.030
334
CPL005 Capillary Disease 36 0.030
335
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 34 0.030
336
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 30 0.030
337
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.030
338
c DYS033 Dysautonomia Like Disorder 16 0.030
339
PLY125 Polycythemia Vera, Somatic 63 0.029
340
LPT001 Leptospirosis 62 0.029
341
P THR003 Thoracic Aortic Aneurysm 57 0.029
342
P HYP083 Hypopituitarism 54 0.029
343
PTT049 Pituitary Adenoma, Acth-Secreting 53 0.029
344
P STR020 Strabismus 51 0.029
345
PST021 Postpartum Depression 49 0.029
346
c CNG411 Congenital Disorder of Glycosylation, Type in 49 0.029
347
URN003 Urinary Schistosomiasis 48 0.029
348
BRN056 Bronchopulmonary Dysplasia 48 0.029
349
GGR001 Geographic Tongue 46 0.029
350
HYP085 Hypothalamic Disease 44 0.029
351
PRD004 Prediabetes Syndrome 43 0.029
352
NRR001 Neuroretinitis 42 0.029
353
BLR008 Bilirubin Metabolic Disorder 42 0.029
354
c ACQ012 Acquired Angioedema 39 0.029
355
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.029
356
MTC005 Mitochondrial Metabolism Disease 36 0.029
357
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.029
358
ISL010 Isolated 17-Linked Lissencephaly 28 0.029
359
NSP003 Nasopharyngeal Disease 26 0.029
360
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 24 0.029
361
VSC009 Vascular Skin Disease 19 0.029
362
ATM013 Autoimmune Disease of Cardiovascular System 13 0.029
363
P DYS007 Dyskeratosis Congenita 63 0.027
364
P NRC002 Narcolepsy 62 0.027
365
TKY002 Takayasu Arteritis 61 0.027
366
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 57 0.027
367
GLL022 Guillain-Barre Syndrome 56 0.027
368
c MYT020 Myotonic Dystrophy 2 56 0.027
369
PLS006 Plasmodium Vivax Malaria 53 0.027
370
ACH005 Achalasia 52 0.027
371
P DRM007 Dermatitis Herpetiformis 51 0.027
372
ATR002 Atransferrinemia 48 0.027
373
FML089 Familial Thoracic Aortic Aneurysm and Dissection 46 0.027
374
TBR006 Tuberculoid Leprosy 43 0.027
375
P SLL003 Salla Disease 43 0.027
376
ACT087 Acth Deficiency 43 0.027
377
SYN031 Synovial Chondromatosis 42 0.027
378
ESN002 Eosinophilia-Myalgia Syndrome 42 0.027
379
MRB001 Marburg Hemorrhagic Fever 41 0.027
380
PHM001 Phimosis 37 0.027
381
FNC002 Functional Diarrhea 37 0.027
382
FLC001 Folic Acid Deficiency Anemia 34 0.027
383
MLN003 Melancholia 34 0.027
384
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 0.027
385
MDY006 Mody, Type Iv 30 0.027
386
c AML016 Amelogenesis Imperfecta, Type 1e 30 0.027
387
IMM070 Immunodeficiency 13 27 0.027
388
LGD001 Leg Dermatosis 16 0.027
389
ORL014 Oral Pharyngeal Disorders 11 0.027
390
P CRG003 Crigler-Najjar Syndrome, Type I 59 0.025
391
LYS001 Loeys-Dietz Syndrome 58 0.025
392
P AVS004 Avascular Necrosis of the Femoral Head 56 0.025
393
P EXP004 Exophthalmos 53 0.025
394
c PRM012 Primary Polycythemia 52 0.025
395
RHM028 Rheumatic Heart Disease 50 0.025
396
WHP001 Whipple Disease 49 0.025
397
TWN001 Twin-to-Twin Transfusion Syndrome 48 0.025
398
MCR191 Microscopic Colitis 47 0.025
399
PST095 Post-Thrombotic Syndrome 47 0.025
400
ALB002 Albinism 46 0.025
401
IDP024 Idiopathic Inflammatory Myopathy 46 0.025
402
ADN001 Adenosine Deaminase Deficiency 45 0.025
403
PNT038 Peanut Allergy 44 0.025
404
PRM020 Premenstrual Tension 44 0.025
405
BMF001 Bamforth-Lazarus Syndrome 42 0.025
406
MCR017 Macrocytic Anemia 42 0.025
407
RCR004 Recurrent Respiratory Papillomatosis 42 0.025
408
PRC003 Proctitis 41 0.025
409
DNT001 Dental Fluorosis 41 0.025
410
FTL021 Fetal Macrosomia 41 0.025
411
c CHR546 Chronic Mountain Sickness 40 0.025
412
DYS015 Dysentery 40 0.025
413
PRX034 Peroxisome Disorders 39 0.025
414
PRL019 Prolidase Deficiency 38 0.025
415
CYC007 Cyclic Thrombocytopenia 37 0.025
416
PNL013 Penile Disease 34 0.025
417
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 34 0.025
418
SPN185 Spinal Cord Infarction 34 0.025
419
FNT004 Fainting 33 0.025
420
ACT056 Acute Cor Pulmonale 33 0.025
421
GGN002 Gigantism 32 0.025
422
LVD002 Livedoid Vasculopathy 32 0.025
423
TMT002 Temtamy Preaxial Brachydactyly Syndrome 27 0.025
424
c DMN028 Diamond-Blackfan Anemia 12 27 0.025
425
KTT001 Ketothiolase Deficiency 24 0.025
426
SBC016 Subacute Delirium 24 0.025
427
RHM029 Rheumatic Fever-Related Antigen Rheumatic Fever, Acute, Susceptibility to, Included 23 0.025
428
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 22 0.025
429
ULC005 Ulcer of Lower Limbs 20 0.025
430
HMG024 Hemoglobinopathy Toms River 5 0.025