Search results for "iron overload"

The MalaCard for "iron overload" has been retired.
Searching MalaCards for entries containing "iron overload"

634 hits were found for 'iron overload'

# Family MCID Name MIFTS Score
1
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 14 7.794
2
IRN008 Iron Overload in Africa 29 6.965
3
c HMC034 Hemochromatosis, Type 5 29 6.324
4
c ANM027 Anemia, Hypochromic Microcytic, with Iron Overload 2 19 6.317
5
GRC001 Gracile Syndrome 32 5.204
6
ANM030 Anemia, Hypochromic Microcytic 37 5.201
7
GNT037 Genetic Hyperferritinemia Without Iron Overload 5 2.619
8
c HMC009 Hemochromatosis Type 2 35 2.614
9
FRR002 Ferro-Cerebro-Cutaneous Syndrome 9 2.589
10
c PRX059 Peroxisome Biogenesis Disorder 1a 52 2.573
11
DFC004 Deficiency Anemia 65 0.565
12
P HMC003 Hemochromatosis 72 0.440
13
IRN001 Iron Deficiency Anemia 51 0.434
14
IRN002 Iron Metabolism Disease 43 0.430
15
P THL005 Thalassemia 61 0.390
16
TNP003 Tn Polyagglutination Syndrome, Somatic 44 0.319
17
P HPT021 Hepatitis 70 0.317
18
THL018 Thalassemia Major 42 0.265
19
NTR005 Nutritional Deficiency Disease 39 0.255
20
LPD004 Lipoid Nephrosis 48 0.247
21
P HML002 Hemolytic Anemia 60 0.215
22
HMG005 Hemoglobinopathy 50 0.214
23
THL017 Thalassemia Intermedia 40 0.213
24
THL010 Thalassemia Minor 38 0.208
25
c CNG027 Congenital Hemolytic Anemia 48 0.207
26
MYL009 Myelodysplastic Syndrome 74 0.198
27
HPT023 Hepatocellular Carcinoma 91 0.191
28
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.188
29
HMS001 Hemosiderosis 45 0.182
30
SCK003 Sickle Cell Anemia 68 0.179
31
SCK005 Sickle Cell Disease 49 0.178
32
c HPT001 Hepatitis C 68 0.177
33
P LVR013 Liver Disease 72 0.173
34
P SDR002 Siderosis 44 0.168
35
MRC001 Marchiafava Bignami Disease 50 0.166
36
MRG013 Mirage Syndrome 26 0.163
37
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.153
38
BNM001 Bone Marrow Cancer 52 0.151
39
P LKM002 Leukemia 70 0.150
40
P PRP029 Porphyria 58 0.150
41
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.144
42
P PRP003 Porphyria Cutanea Tarda 64 0.143
43
IMP003 Impaired Renal Function Disease 37 0.142
44
NRN002 Neuronitis 42 0.141
45
P HRT032 Heart Disease 76 0.139
46
c INH020 Inherited Metabolic Disorder 49 0.139
47
c PRM023 Pre-Malignant Neoplasm 43 0.137
48
MCR018 Microcytic Anemia 42 0.137
49
c HMC010 Hemochromatosis, Type 3 38 0.137
50
P APL001 Aplastic Anemia 73 0.136
51
HYP266 Hypoxia 55 0.136
52
CNG034 Congestive Heart Failure 71 0.135
53
c CHR089 Chronic Kidney Failure 66 0.129
54
HMT018 Hematopoietic Stem Cell Transplantation 41 0.127
55
P SDR003 Sideroblastic Anemia 39 0.125
56
NNL002 Nonalcoholic Steatohepatitis 53 0.121
57
END072 Endotheliitis 42 0.118
58
MTL002 Metal Metabolism Disorder 38 0.118
59
P CRD011 Cardiomyopathy 67 0.114
60
LVR012 Liver Cirrhosis 67 0.112
61
c ACT073 Acute Leukemia 62 0.112
62
P SCK034 Sickle Beta Thalassemia 31 0.112
63
MTH009 Mouth Disease 63 0.112
64
c CRN214 Coronary Heart Disease 5 23 0.111
65
HRT007 Heart Cancer 50 0.110
66
P HRT017 Heart Tumor 35 0.110
67
c ADL079 Adult Heart Tumor 19 0.110
68
c HPT073 Hepatitis C Virus 72 0.107
69
URN009 Urinary System Disease 53 0.106
70
P URF003 Urofacial Syndrome 1 52 0.105
71
c HMG004 Hemoglobin D Disease 33 0.104
72
VTM003 Vitamin Metabolic Disorder 33 0.104
73
HMT002 Hematologic Cancer 64 0.104
74
c CRN172 Coronary Heart Disease 3 21 0.103
75
CNG028 Congenital Hypoplastic Anemia 49 0.103
76
P CRN178 Coronary Heart Disease 6 24 0.103
77
ACR006 Aceruloplasminemia 43 0.103
78
DDN006 Duodenitis 44 0.102
79
END030 End Stage Renal Failure 52 0.102
80
c HMG001 Hemoglobin C Disease 47 0.101
81
P OBS005 Obesity 93 0.101
82
P MYL006 Myeloid Leukemia 67 0.100
83
ADL002 Adult Syndrome 53 0.100
84
PLS009 Plasma Cell Neoplasm 48 0.100
85
PNC034 Pancreas Disease 57 0.098
86
c PNC106 Pancreatic Agenesis 1 40 0.098
87
P ATX004 Ataxia 53 0.098
88
RFR010 Refractory Anemia 45 0.098
89
ACD009 Acid-Labile Subunit, Deficiency of 48 0.098
90
P DMN001 Diamond-Blackfan Anemia 68 0.097
91
TBR010 Tuberculosis 69 0.097
92
RTN023 Retinitis 49 0.097
93
HRT029 Heart Tumor of the Child 17 0.096
94
FTT001 Fatty Liver Disease 60 0.093
95
PYR013 Pyruvate Kinase Deficiency 58 0.092
96
ALR002 Al-Raqad Syndrome 36 0.092
97
P ART022 Arthritis 75 0.092
98
SNG003 Single Ventricular Heart 24 0.091
99
P LYM026 Lymphoblastic Leukemia 60 0.089
100
PRR002 Pure Red-Cell Aplasia 46 0.089
101
P KDN017 Kidney Cancer 67 0.088
102
c HMG003 Hemoglobin E Disease 44 0.088
103
P LYM118 Lymphoma 70 0.087
104
c CRN177 Coronary Heart Disease 7 22 0.087
105
PRP027 Peripheral Vascular Disease 69 0.086
106
P PLM037 Pulmonary Hypertension 79 0.085
107
c CRN173 Coronary Heart Disease 8 20 0.085
108
P LYM033 Lymphoproliferative Syndrome 53 0.084
109
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 31 0.083
110
ACT118 Acute Non Lymphoblastic Leukemia 29 0.083
111
BLD054 Blood Protein Disease 40 0.083
112
c CRN175 Coronary Heart Disease 4 21 0.083
113
HYP080 Hypogonadism 54 0.082
114
LYM023 Lymphatic System Cancer 35 0.082
115
ADJ001 Adjustment Disorder 38 0.082
116
c CHR064 Chronic Monocytic Leukemia 43 0.082
117
P MYL005 Myelofibrosis 67 0.081
118
LYM067 Lymphoid Leukemia 43 0.081
119
P HYP086 Hypothyroidism 65 0.081
120
ANM029 Anemia, Sideroblastic, X-Linked 49 0.081
121
c LKM061 Leukemia, Acute Myeloid 71 0.080
122
P FRD001 Friedreich Ataxia 62 0.080
123
PLS010 Plasma Protein Metabolism Disease 38 0.080
124
PCK002 Pick Disease 67 0.078
125
P MLT019 Multiple Myeloma 80 0.078
126
ATR060 Atrial Standstill, Digenic 53 0.078
127
PLC008 Placenta Disease 36 0.078
128
P HYP060 Hyperinsulinism 59 0.078
129
SYS003 Systolic Heart Failure 43 0.078
130
VSC008 Vascular Hemostatic Disease 33 0.077
131
CRB009 Cerebritis 38 0.077
132
LYM024 Lymphatic System Disease 50 0.076
133
c LKM062 Leukemia, Acute Lymphoblastic 64 0.076
134
P ACT074 Acute Lymphocytic Leukemia 55 0.076
135
LYM040 Lymphoblastic Lymphoma 54 0.076
136
c ADL052 Adult Acute Lymphocytic Leukemia 42 0.076
137
P CNG003 Congenital Dyserythropoietic Anemia 39 0.076
138
c LYM107 Lymphoproliferative Syndrome 2 34 0.076
139
BNL002 Bone Lymphoma 33 0.076
140
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.076
141
PRM151 Primary Bone Lymphoma 27 0.076
142
c DMN005 Diamond-Blackfan Anemia 2 23 0.076
143
c LKM055 Leukemia, Acute Lymphoblastic 2 22 0.076
144
P CTR002 Cataract 57 0.076
145
c VRL010 Viral Hepatitis 61 0.076
146
ISC004 Ischemia 59 0.076
147
P HMR003 Hemorrhagic Disease 57 0.076
148
c CRN174 Coronary Heart Disease 2 22 0.076
149
SPL012 Splenic Disease 47 0.075
150
IMM127 Immune System Cancer 42 0.075
151
P BLD051 Blood Coagulation Disease 45 0.074
152
c TRC078 Trichohepatoenteric Syndrome 2 31 0.073
153
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.073
154
CHL071 Child Syndrome 58 0.073
155
KDS001 Kid Syndrome 53 0.073
156
c DMN023 Diamond-Blackfan Anemia 1 38 0.072
157
VND001 Vein Disease 52 0.071
158
CMP005 Campomelic Dysplasia 72 0.071
159
P ACQ009 Acquired Metabolic Disease 41 0.071
160
LYM019 Lymphosarcoma 53 0.071
161
c HMC035 Hemochromatosis, Type 4 39 0.071
162
GLT021 Glutaricaciduria, Type I 48 0.070
163
HYP099 Hyperferritinemia-Cataract Syndrome 42 0.070
164
VSC006 Vascular Cancer 54 0.070
165
PLS016 Plasma Cell Leukemia 42 0.070
166
c ADL001 Adult Lymphoma 41 0.070
167
RFR004 Refractory Hematologic Cancer 29 0.070
168
c LKM060 Leukemia, Acute Lymphoblastic 3 52 0.069
169
c LYM106 Lymphoproliferative Syndrome 1 34 0.069
170
ACR041 Acromelic Frontonasal Dysostosis 46 0.068
171
ATH003 Atherosclerosis 62 0.068
172
ALL026 Allergic Hypersensitivity Disease 53 0.068
173
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.068
174
P RTN016 Retinal Degeneration 54 0.068
175
CSY001 C Syndrome 49 0.068
176
c CHR418 Chronic Leukemia 48 0.068
177
CRD118 Cardiovascular Cancer 47 0.068
178
PLS003 Plasmacytic Leukemia 23 0.068
179
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.067
180
P ADN016 Adenocarcinoma 69 0.067
181
P MYP004 Myopathy 67 0.067
182
INT253 Intestinal Benign Neoplasm 50 0.067
183
WLS001 Wilson Disease 72 0.066
184
P NRB001 Neuroblastoma 69 0.066
185
P SPS003 Spastic Diplegia 53 0.066
186
BRT030 Birth Defects 43 0.066
187
MSC004 Muscle Tissue Disease 36 0.066
188
P HRD011 Hereditary Spherocytosis 53 0.066
189
BNC003 Bone Cancer 45 0.066
190
SPL011 Spleen Cancer 37 0.066
191
ANG049 Angioedema Induced by Ace Inhibitors 35 0.065
192
c DMN024 Diamond-Blackfan Anemia 7 28 0.065
193
c HPT016 Hepatitis B 64 0.065
194
LPD008 Lipid Metabolism Disorder 58 0.065
195
c CHR096 Chronic Pulmonary Heart Disease 40 0.064
196
c ACT020 Acute T Cell Leukemia 39 0.064
197
P BRS047 Breast Cancer 100 0.064
198
HV1006 Hiv-1 82 0.063
199
ADN018 Adenoma 59 0.063
200
WLL006 Wells Syndrome 56 0.063
201
GDS001 Good Syndrome 45 0.063
202
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.063
203
AMN006 Aminoaciduria 42 0.063
204
HMG015 Hemoglobin S Beta-Thalassemia 17 0.063
205
ALN001 Aland Island Eye Disease 45 0.063
206
PRM025 Primary Bacterial Infectious Disease 43 0.063
207
MNR003 Mineral Metabolism Disease 41 0.063
208
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.063
209
P LCT001 Lactic Acidosis 52 0.062
210
BRN106 Burns 52 0.062
211
c SCK008 Sickle Delta Beta Thalassemia 11 0.062
212
c CHR090 Chronic Lymphocytic Leukemia 74 0.062
213
P INF032 Infertility 61 0.062
214
EXF001 Exfoliation Syndrome 57 0.062
215
P PLN008 Peeling Skin Syndrome 47 0.062
216
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.062
217
ANX002 Anxiety Disorder 69 0.061
218
c FNC027 Fanconi Anemia, Complementation Group a 73 0.060
219
P LKM068 Leukemia, Chronic Myeloid, Somatic 66 0.060
220
P OST002 Osteoporosis 64 0.060
221
MSS002 Mass Syndrome 59 0.060
222
P MLT074 Multiple Endocrine Neoplasia 55 0.060
223
FRB001 Farber Lipogranulomatosis 51 0.060
224
P FNC026 Fanconi Renotubular Syndrome 1 51 0.060
225
MYL004 Myelodysplastic Myeloproliferative Cancer 47 0.060
226
ATN005 Autonomic Dysfunction 45 0.060
227
P CHR562 Chronic Myelocytic Leukemia 41 0.060
228
LVR006 Liver Lymphoma 29 0.060
229
P MYC007 Myocardial Infarction 79 0.060
230
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.060
231
P ENC018 Encephalopathy 59 0.060
232
PHY002 Physical Disorder 44 0.060
233
CNT098 Central Core Disease 66 0.060
234
LYM115 Lymphoma, Non-Hodgkin 65 0.060
235
P BCL006 B-Cell Lymphomas 64 0.060
236
P NRV006 Nervous System Cancer 62 0.060
237
INT066 Interstitial Lung Disease 58 0.060
238
c LKM004 Leukemia, B-Cell, Chronic 25 0.060
239
c LKM050 Leukemia, Chronic Lymphocytic 1 22 0.060
240
c LKM051 Leukemia, Chronic Lymphocytic 3 22 0.060
241
c HYP595 Hypertension, Essential 69 0.058
242
P PNM006 Pneumoconiosis 51 0.058
243
GRW007 Growth Hormone Deficiency 48 0.058
244
P PRS040 Prostate Cancer 89 0.058
245
P OST012 Osteoarthritis 82 0.058
246
P FLL037 Follicular Lymphoma 66 0.058
247
P ART023 Arthropathy 63 0.058
248
P ESP024 Esophagitis 62 0.058
249
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.058
250
LYM104 Lymphoma, Malt, Somatic 54 0.058
251
END035 Endocrine Gland Cancer 52 0.058
252
MRG003 Marginal Zone B-Cell Lymphoma 50 0.058
253
c FLL041 Follicular Lymphoma 1 46 0.058
254
SPL004 Splenic Marginal Zone Lymphoma 43 0.058
255
CLL014 Cll/sll 43 0.058
256
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.058
257
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.058
258
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 35 0.058
259
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 31 0.058
260
c LKM056 Leukemia, Chronic Lymphocytic 2 24 0.058
261
RFR001 Refractory Plasma Cell Neoplasm 18 0.058
262
c ACT071 Acute Kidney Failure 50 0.058
263
RNL025 Renal Hypoplasia 41 0.058
264
c DMN021 Diamond-Blackfan Anemia 6 36 0.058
265
c DMN017 Diamond-Blackfan Anemia 10 30 0.058
266
VSC001 Vascular Myelopathy 25 0.058
267
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 17 0.058
268
CHL068 Cholestasis 58 0.057
269
FML039 Female Reproductive System Disease 48 0.057
270
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.057
271
P MDL005 Medulloblastoma 77 0.056
272
HDG012 Hodgkin Lymphoma 73 0.056
273
MNT001 Mantle Cell Lymphoma 70 0.056
274
c ADL017 Adult T-Cell Leukemia 58 0.056
275
PRS047 Prostatitis 56 0.056
276
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.056
277
P CTN015 Cutaneous T Cell Lymphoma 50 0.056
278
ATN002 Autonomic Nervous System Disease 47 0.056
279
LKC003 Leukocyte Disease 47 0.056
280
MXD023 Mixed Cell Type Cancer 47 0.056
281
P TCL004 T-Cell Leukemia 46 0.056
282
VSC047 Vascular Malformation 45 0.056
283
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.056
284
VSC018 Visceral Steatosis 37 0.056
285
HDG004 Hodgkin's Granuloma 26 0.056
286
c LKM005 Leukemia, T-Cell, Chronic 22 0.056
287
HDG006 Hodgkin's Paragranuloma 20 0.056
288
RSP006 Respiratory System Disease 62 0.055
289
OCL009 Ocular Cancer 62 0.055
290
P MSC033 Muscle Disorders 52 0.055
291
TST021 Testicular Germ Cell Tumor 70 0.054
292
MYC006 Mycosis Fungoides 66 0.054
293
BRK010 Burkitt Lymphoma 66 0.054
294
EWN003 Ewing Sarcoma 64 0.054
295
P NRP001 Neuropathy 60 0.054
296
ANR040 Aneurysm 57 0.054
297
DFF005 Diffuse Large B-Cell Lymphoma 56 0.054
298
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.054
299
SZR001 Sezary's Disease 53 0.054
300
RTC005 Reticulosarcoma 48 0.054
301
PTT009 Pituitary Gland Disease 48 0.054
302
RTC009 Reticulum Cell Sarcoma 48 0.054
303
PLS025 Plasmablastic Lymphoma 45 0.054
304
GND003 Gonadal Disease 43 0.054
305
GRM001 Germ Cell and Embryonal Cancer 39 0.054
306
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.054
307
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 28 0.054
308
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 0.054
309
PRM128 Primary Cutaneous Follicle Center Lymphoma 26 0.054
310
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 22 0.054
311
BND002 B- and T-Cell Mixed Leukemia 20 0.054
312
HML018 Homologous Wasting Disease 17 0.054
313
P CRN211 Coronary Artery Disease 75 0.054
314
LNG099 Lung Disease 62 0.054
315
LRN003 Learning Disability 51 0.054
316
P TRC086 Trichohepatoenteric Syndrome 1 46 0.054
317
c PLN021 Peeling Skin Syndrome 3 31 0.054
318
P HYP024 Hypoparathyroidism 52 0.052
319
P RNL015 Renal Hypertension 47 0.052
320
ART111 Artery Disease 57 0.052
321
BRN071 Brain Injury 52 0.052
322
GLC008 Glucose Metabolism Disease 47 0.052
323
P OVR042 Ovarian Cancer 75 0.052
324
c MLT024 Multiple Endocrine Neoplasia Iia 65 0.052
325
WST001 West Syndrome 61 0.052
326
P ALC004 Alcohol Abuse 60 0.052
327
P OVR049 Ovarian Disease 55 0.052
328
GLM004 Gliomatosis Cerebri 53 0.052
329
CHL061 Childhood Leukemia 48 0.052
330
BLR008 Bilirubin Metabolic Disorder 47 0.052
331
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.052
332
ANX004 Anoxia 44 0.052
333
END038 Endocrine Pancreas Disease 43 0.052
334
HPT067 Hepatocellular Adenoma 42 0.052
335
c NRB015 Neuroblastoma 2 31 0.052
336
ARG006 Aregenerative Anemia 23 0.052
337
c CRN176 Coronary Heart Disease 9 20 0.052
338
c NRB013 Neuroblastoma 6 19 0.052
339
P PNC035 Pancreatic Cancer 85 0.050
340
c HPT003 Hepatitis a 59 0.050
341
P LTR001 Lateral Sclerosis 52 0.050
342
AYM001 Ayme-Gripp Syndrome 45 0.050
343
c PLN018 Peeling Skin Syndrome 2 35 0.050
344
c PLN017 Peeling Skin Syndrome 1 33 0.050
345
ZYG002 Zygomycosis 33 0.050
346
c MLT136 Multiple Endocrine Neoplasia 1 68 0.049
347
PLM033 Pulmonary Embolism 59 0.049
348
ABL002 Ablepharon-Macrostomia Syndrome 57 0.049
349
CHR285 Chronic Myelomonocytic Leukemia 55 0.049
350
TST014 Testicular Cancer 52 0.049
351
c CHR417 Chronic Graft Versus Host Disease 50 0.049
352
URM002 Uremia 50 0.049
353
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 48 0.049
354
DST006 Diastolic Heart Failure 46 0.049
355
TST015 Testicular Disease 45 0.049
356
OVR094 Ovarian Epithelial Cancer 45 0.049
357
PRP036 Peripheral T-Cell Lymphoma 45 0.049
358
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.049
359
EPS006 Epstein Syndrome 40 0.049
360
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.049
361
LYM127 Lymphatic Malformations 37 0.049
362
TST004 Testicular Lymphoma 37 0.049
363
OVR021 Ovarian Lymphoma 33 0.049
364
TST003 Testicular Leukemia 32 0.049
365
BRS001 Breast Lymphoma 32 0.049
366
c DMN006 Diamond-Blackfan Anemia 3 30 0.049
367
DFF027 Diffuse Lymphatic Malformation 30 0.049
368
OVR056 Ovarian Primitive Germ Cell Tumor 29 0.049
369
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 29 0.049
370
HFS001 Hfe-Associated Hereditary Hemochromatosis 28 0.049
371
c DMN020 Diamond-Blackfan Anemia 8 27 0.049
372
P ABD016 Abdominal Obesity-Metabolic Syndrome 26 0.049
373
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 25 0.049
374
PRM200 Primary Fanconi Syndrome 24 0.049
375
OVR069 Ovarian Germ Cell Tumor 23 0.049
376
BNP001 Bone Peripheral Neuroepithelioma 18 0.049
377
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 17 0.049
378
P MSC007 Muscle Hypertrophy 59 0.049
379
P ESN007 Eosinophilia 61 0.048
380
ETN001 Eating Disorder 60 0.048
381
PLS011 Plasmacytoma 56 0.048
382
P PNC001 Pancytopenia 52 0.048
383
NSD001 Nose Disease 52 0.048
384
THY030 Thyroid Gland Disease 51 0.048
385
BRN004 Brain Edema 51 0.048
386
MCR004 Macroglobulinemia 50 0.048
387
c HMC021 Hemochromatosis, Type 2a 28 0.048
388
HMC038 Hemochromatosis, Neonatal 27 0.048
389
ANP010 Anaplastic Plasmacytoma 21 0.048
390
c DLT001 Delta Chain Disease 16 0.048
391
P HYP117 Hypertriglyceridemia 65 0.046
392
P MYC008 Myocarditis 54 0.046
393
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.046
394
P HRT035 Heart Block, Congenital 39 0.046
395
c DMN022 Diamond-Blackfan Anemia 9 27 0.046
396
VBR003 Vibrio Vulnificus Infection 23 0.046
397
c TFR001 Tfr2-Related Hereditary Hemochromatosis 12 0.046
398
SKN016 Skin Disease 68 0.046
399
P EPL164 Epilepsy 66 0.046
400
CNN005 Connective Tissue Disease 61 0.046
401
P ADL010 Adult Respiratory Distress Syndrome 60 0.046
402
P HST010 Histiocytosis 55 0.046
403
FML038 Female Reproductive Organ Cancer 51 0.046
404
FML037 Female Breast Cancer 51 0.046
405
P DYS021 Dysautonomia 47 0.046
406
SXL003 Sexual Disorder 47 0.046
407
MLR006 Male Reproductive Organ Cancer 47 0.046
408
NTR003 Natural Killer Cell Leukemia 47 0.046
409
BLD053 Blood Platelet Disease 46 0.046
410
GRN017 Granulocytopenia 42 0.046
411
ANT018 Anthracosis 42 0.046
412
MYF002 Myofascial Pain Syndrome 40 0.046
413
SXD001 Sex Differentiation Disease 40 0.046
414
MLR007 Male Reproductive System Disease 37 0.046
415
LPD027 Lip Disease 36 0.046
416
CTN011 Cutaneous Porphyria 31 0.046
417
P GNR027 Generalized Peeling Skin Syndrome 22 0.046
418
c DYS033 Dysautonomia Like Disorder 19 0.046
419
BRN028 Brain Cancer 70 0.044
420
ART016 Aortic Aneurysm 67 0.044
421
P WLD002 Waldenstrom Macroglobulinemia 62 0.044
422
HRY003 Hairy Cell Leukemia 60 0.044
423
VRL011 Viral Infectious Disease 59 0.044
424
ALC006 Alcoholic Hepatitis 59 0.044
425
P ANP001 Anaplastic Large Cell Lymphoma 58 0.044
426
STR026 Star Syndrome 56 0.044
427
JNT002 Joint Disorders 56 0.044
428
P MMB011 Membranous Nephropathy 56 0.044
429
PST046 Post-Transplant Lymphoproliferative Disease 53 0.044
430
P ACT135 Acute Graft Versus Host Disease 53 0.044
431
P LPC002 Lip Cancer 53 0.044
432
INT007 Intermediate Coronary Syndrome 52 0.044
433
c HPT015 Hepatitis D 52 0.044
434
MST017 Mast Cell Disease 52 0.044
435
CLN015 Colon Adenocarcinoma 49 0.044
436
MST002 Mast-Cell Leukemia 48 0.044
437
LYM051 Lymphomatoid Granulomatosis 46 0.044
438
ANG046 Angioimmunoblastic T-Cell Lymphoma 45 0.044
439
P ABD003 Abdominal Aortic Aneurysm 43 0.044
440
MST006 Mast Syndrome 43 0.044
441
MST004 Mast Cell Neoplasm 42 0.044
442
BND014 Bone Development Disease 42 0.044
443
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 41 0.044
444
PRM026 Primary Systemic Mycosis 41 0.044
445
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.044
446
SPC003 Specific Developmental Disorder 40 0.044
447
SLT001 Solitary Osseous Plasmacytoma 38 0.044
448
ACR002 Acrocapitofemoral Dysplasia 36 0.044
449
c CNN010 Connective Tissue Benign Neoplasm 35 0.044
450
RNL021 Renal Tubular Transport Disease 35 0.044
451
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 34 0.044
452
RFR002 Refractory Hairy Cell Leukemia 31 0.044
453
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.044
454
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 25 0.044
455
c MCR162 Macroglobulinemia, Waldenstrom 2 20 0.044
456
HRY001 Hairy Cell Leukemia of Spleen 18 0.044
457
c ANP011 Anaplastic Small Cell Lymphoma 17 0.044
458
PRM165 Primary Plasmacytoma of the Bone 15 0.044
459
GTR002 Goiter 54 0.043
460
P TYR004 Tyrosinemia 45 0.043
461
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 23 0.043
462
ESP021 Esophageal Cancer 75 0.041
463
CHR066 Chronic Fatigue Syndrome 64 0.041
464
P SPN301 Spinocerebellar Ataxia 2 63 0.041
465
c SVR001 Severe Acute Respiratory Syndrome 57 0.041
466
SBS003 Substance Abuse 56 0.041
467
P SML016 Small Intestine Cancer 54 0.041
468
THL016 Thalassemias, Alpha- 54 0.041
469
TTH006 Tooth Disease 52 0.041
470
c HMN021 Human T-Cell Leukemia Virus Type 1 51 0.041
471
MYC002 Mycobacterium Avium Complex Disease 51 0.041
472
HPT074 Hepatic Adenoma, Somatic 51 0.041
473
OCL006 Ocular Hypertension 48 0.041
474
ATR002 Atransferrinemia 47 0.041
475
INT054 Intraocular Lymphoma 45 0.041
476
P CNN004 Connective Tissue Cancer 45 0.041
477
RNL097 Renal Artery Disease 45 0.041
478
CHR008 Choroiditis 43 0.041
479
PRP080 Peripheral Artery Disease 36 0.041
480
GLB003 Globe Disease 35 0.041
481
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 35 0.041
482
INT271 Interstitial Lung and Liver Disease 34 0.041
483
c EYL003 Eye Lymphoma 33 0.041
484
c NRB014 Neuroblastoma 3 30 0.041
485
c DMN019 Diamond-Blackfan Anemia 4 28 0.041
486
HNM002 Hinman Syndrome 25 0.041
487
ACQ016 Acquired Pure Red Cell Aplasia 24 0.041
488
HPD002 Hepadnavirus Infection 23 0.041
489
XLN067 X-Linked Protoporphyria 22 0.041
490
c NRB012 Neuroblastoma 5 20 0.041
491
LPN002 Lip and Oral Cavity Cancer 18 0.041
492
MLG026 Male Genital Organ Vascular Disease 17 0.041
493
P ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 11 0.041
494
ADP002 Adiponectin Deficiency 31 0.038
495
BLN006 Blind Loop Syndrome 30 0.038
496
P SCH015 Schizophrenia 76 0.038
497
ISC006 Ischemic Heart Disease 68 0.038
498
THY028 Thyroid Cancer 68 0.038
499
ALC007 Alcohol Dependence 65 0.038
500
P CMR001 Camurati-Engelmann Disease 59 0.038
501
c SYS004 Systemic Mastocytosis 59 0.038
502
P HYP069 Hyperparathyroidism 57 0.038
503
P BRN009 Burning Mouth Syndrome 57 0.038
504
PLM010 Pulmonary Edema 56 0.038
505
TTH002 Tooth Agenesis 55 0.038
506
P PRP019 Peripheral Nervous System Disease 54 0.038
507
P MST009 Mastocytosis 54 0.038
508
LTT002 Letterer-Siwe Disease 54 0.038
509
BLM002 Bulimia Nervosa 54 0.038
510
P GND004 Gonadal Dysgenesis 53 0.038
511
MSC072 Muscle Cancer 51 0.038
512
P HYP098 Hypereosinophilic Syndrome 51 0.038
513
CRN030 Coronary Stenosis 50 0.038
514
c MLT086 Multiple Endocrine Neoplasia, Type Iv 49 0.038
515
HYD046 Hydatidiform Mole, Recurrent, 1 49 0.038
516
CTN014 Cutaneous Mastocytosis 48 0.038
517
ADR038 Adermatoglyphia 48 0.038
518
HND003 Hand-Foot-Uterus Syndrome 47 0.038
519
CHR563 Chronic Eosinophilic Leukemia 47 0.038
520
ATY042 Atypical Chronic Myeloid Leukemia 45 0.038
521
PTT037 Pituitary Tumors 45 0.038
522
c MTR002 Mitral Valve Insufficiency 44 0.038
523
c HMN022 Human T-Cell Leukemia Virus Type 2 44 0.038
524
CHR286 Chronic Neutrophilic Leukemia 44 0.038
525
SML008 Small Intestine Lymphoma 41 0.038
526
CYS036 Cystinosis, Nephropathic 41 0.038
527
DFF001 Diffuse Cutaneous Mastocytosis 41 0.038
528
HPT070 Hepatosplenic T-Cell Lymphoma 41 0.038
529
P TST026 Testicular Germ Cell Cancer 41 0.038
530
LNG013 Lung Lymphoma 40 0.038
531
c PRM149 Primary Hypereosinophilic Syndrome 39 0.038
532
NSY001 N Syndrome 39 0.038
533
SBS006 Sebastian Syndrome 37 0.038
534
TRP005 Trophoblastic Neoplasm 36 0.038
535
MLG088 Malignant Germ Cell Tumor 36 0.038
536
P MXD016 Mixed Gonadal Dysgenesis 36 0.038
537
MYL015 Myeloproliferative Disorder with Eosinophilia 35 0.038
538
P OVR075 Ovarian Dysgenesis 1 34 0.038
539
MXD025 Mixed Germ Cell Cancer 33 0.038
540
c OVR076 Ovarian Dysgenesis 2 33 0.038
541
CVT001 Cavitary Optic Disc Anomalies 32 0.038
542
MXD032 Mixed Germ Cell Tumor 31 0.038
543
c PNC111 Pancreatic Cancer 2 30 0.038
544
c DMN018 Diamond-Blackfan Anemia 5 29 0.038
545
c PNC094 Pancreatic Cancer 1 29 0.038
546
UND007 Undifferentiated Connective Tissue Disease 29 0.038
547
GST059 Gestational Trophoblastic Tumor 28 0.038
548
c DMN028 Diamond-Blackfan Anemia 12 27 0.038
549
c OVR102 Ovarian Dysgenesis 3 25 0.038
550
PRM133 Primary Pulmonary Lymphoma 24 0.038
551
c TST017 Testicular Malignant Germ Cell Cancer 24 0.038
552
SCK020 Sickle Cell - Hemoglobin D Disease 24 0.038
553
OVR015 Ovarian Mixed Germ Cell Neoplasm 22 0.038
554
VSC009 Vascular Skin Disease 22 0.038
555
ADL082 Adult Pulmonary Langerhans Cell Histiocytosis 22 0.038
556
NRC007 Neuroectodermal Endocrine Syndrome 22 0.038
557
TST040 Testicular Trophoblastic Tumor 21 0.038
558
DSS003 Disseminated Eosinophilic Collagen Disease 18 0.038
559
WSC001 Wisconsin Syndrome 17 0.038
560
c SML023 Small Cell Lung Cancer, Adult 17 0.038
561
ISL032 Isolated Bone Marrow Mastocytosis 16 0.038
562
LYM117 Lymphocytic Hypereosinophilic Syndrome 16 0.038
563
c HMN023 Human T-Cell Leukemia Virus Type 3 16 0.038
564
c SCN042 Secondary Hypereosinophilic Syndrome 16 0.038
565
MXD024 Mixed Epithelial Tumor of Ovary 16 0.038
566
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 15 0.038
567
MLG035 Malignant Ovarian Mixed Epithelial Neoplasm 15 0.038
568
HDG010 Hodgkin Lymphoma, During Pregnancy 14 0.038
569
NNH004 Non-Hodgkin Lymphoma, During Pregnancy 14 0.038
570
P ENC004 Encephalitis 61 0.035
571
BRN002 Bronchiolitis 56 0.035
572
PTT006 Pituitary Adenoma 55 0.035
573
TMR010 Tumor Predisposition Syndrome 52 0.035
574
PRC013 Pericarditis 52 0.035
575
HYP005 Hypokalemia 51 0.035
576
P MSC003 Muscular Atrophy 51 0.035
577
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.035
578
MSS001 Masa Syndrome 49 0.035
579
P APL006 Aplasia Cutis Congenita 48 0.035
580
BNN003 Bone Inflammation Disease 46 0.035
581
HPT046 Hepatic Veno-Occlusive Disease 45 0.035
582
PTT008 Pituitary Carcinoma 44 0.035
583
P PNC045 Pancreatic Agenesis 44 0.035
584
NRR001 Neuroretinitis 42 0.035
585
VGN023 Vaginitis 42 0.035
586
ACT103 Acute Lymphoblastic Leukemia, Childhood 42 0.035
587
HRT012 Heart Valve Disease 41 0.035
588
PDT001 Pediatric Lymphoma 40 0.035
589
NNF001 Non-Functioning Pancreatic Endocrine Tumor 38 0.035
590
MTL005 Metal Allergy 34 0.035
591
JNS003 Jensen Syndrome 34 0.035
592
HRZ001 Huriez Syndrome 33 0.035
593
PTT001 Pituitary Hypoplasia 31 0.035
594
HRT003 Heart Lymphoma 31 0.035
595
PNC092 Pancreatic Agenesis and Congenital Heart Defects 28 0.035
596
c MYL058 Myeloproliferative Syndrome, Transient 23 0.035
597
MNG003 Mungan Syndrome 22 0.035
598
c PNC105 Pancreatic Agenesis 2 22 0.035
599
CRT057 Critical Congenital Heart Disease 20 0.035
600
MYC003 Myocardium Cancer 17 0.035
601
FNC012 Functioning Pancreatic Endocrine Tumor 16 0.035
602
SPT004 Septic Arthritis 59 0.030
603
P MTR012 Mitral Valve Disease 59 0.030
604
P GT001 Gout 58 0.030
605
c ATM011 Autoimmune Hepatitis 58 0.030
606
c SRC025 Sarcoidosis 1 58 0.030
607
CRT002 Cartilage-Hair Hypoplasia 58 0.030
608
P GLM007 Glomerulonephritis 56 0.030
609
LST001 Listeriosis 54 0.030
610
PLM012 Pulmonary Sarcoidosis 54 0.030
611
HPT022 Hepatoblastoma 53 0.030
612
DBN001 Dubin-Johnson Syndrome 52 0.030
613
PRP032 Porphyria Variegata 52 0.030
614
PRC012 Pericardial Effusion 50 0.030
615
HYP037 Hyperhomocysteinemia 50 0.030
616
HPT009 Hepatopulmonary Syndrome 48 0.030
617
RNL077 Renal Fibrosis 47 0.030
618
RNL011 Renal Osteodystrophy 47 0.030
619
HPT014 Hepatorenal Syndrome 46 0.030
620
ADN001 Adenosine Deaminase Deficiency 45 0.030
621
CRD001 Cardiac Tamponade 44 0.030
622
P ART018 Aortic Valve Insufficiency 42 0.030
623
c ATM022 Autoimmune Myocarditis 41 0.030
624
PRR013 Prurigo Nodularis 37 0.030
625
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.030
626
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 32 0.030
627
ATY004 Atypical Neurofibroma 30 0.030
628
ATH010 Athyreosis 30 0.030
629
WRF003 Warfarin Syndrome 28 0.030
630
SPN331 Spondyloocular Syndrome 27 0.030
631
RHS001 Rh Isoimmunization 27 0.030
632
END003 Endometrial Stromal Nodule 23 0.030
633
P STM009 Stomatocytosis I 20 0.030
634
CMP052 Complication in Hemodialysis 16 0.030