Search results for "iron overload"

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

649 hits were found for 'iron overload'

# Family MCID Name MIFTS Score
1
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 15 7.803
2
IRN008 Iron Overload in Africa 29 6.966
3
c HMC034 Hemochromatosis, Type 5 28 5.779
4
c ANM027 Anemia, Hypochromic Microcytic, with Iron Overload 2 20 5.774
5
GRC001 Gracile Syndrome 33 5.206
6
ANM030 Anemia, Hypochromic Microcytic 37 4.547
7
GNT037 Genetic Hyperferritinemia Without Iron Overload 3 2.620
8
c HMC009 Hemochromatosis Type 2 30 2.619
9
FRR002 Ferro-Cerebro-Cutaneous Syndrome 9 2.590
10
P ZLL001 Zellweger Syndrome 49 2.565
11
DFC004 Deficiency Anemia 64 0.562
12
P HMC003 Hemochromatosis 71 0.437
13
IRN001 Iron Deficiency Anemia 51 0.430
14
IRN002 Iron Metabolism Disease 38 0.421
15
P THL005 Thalassemia 61 0.388
16
P HPT021 Hepatitis 74 0.319
17
THL018 Thalassemia Major 31 0.262
18
ANM029 Anemia, Sideroblastic, X-Linked 53 0.249
19
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.248
20
NTR005 Nutritional Deficiency Disease 51 0.236
21
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.225
22
LPD004 Lipoid Nephrosis 49 0.221
23
P HML002 Hemolytic Anemia 60 0.215
24
HMG005 Hemoglobinopathy 49 0.213
25
THL017 Thalassemia Intermedia 38 0.213
26
THL010 Thalassemia Minor 38 0.208
27
c CNG027 Congenital Hemolytic Anemia 46 0.207
28
MYL009 Myelodysplastic Syndrome 73 0.197
29
c CNG401 Congenital Heart Disease 67 0.196
30
HPT023 Hepatocellular Carcinoma 90 0.191
31
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 61 0.187
32
HMS001 Hemosiderosis 42 0.183
33
SCK003 Sickle Cell Anemia 72 0.178
34
SCK005 Sickle Cell Disease 51 0.178
35
c HPT001 Hepatitis C 68 0.176
36
P SDR002 Siderosis 44 0.171
37
P LVR013 Liver Disease 76 0.168
38
MRC001 Marchiafava Bignami Disease 33 0.164
39
SPN041 Spinal Cord Disease 50 0.161
40
P KDN018 Kidney Disease 64 0.156
41
BNM001 Bone Marrow Cancer 56 0.149
42
P PRP029 Porphyria 56 0.148
43
P LKM002 Leukemia 70 0.148
44
MCR018 Microcytic Anemia 41 0.147
45
ACD009 Acid-Labile Subunit, Deficiency of 37 0.143
46
P PRP003 Porphyria Cutanea Tarda 63 0.141
47
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.140
48
NRN002 Neuronitis 40 0.140
49
c INH020 Inherited Metabolic Disorder 49 0.139
50
IMP003 Impaired Renal Function Disease 36 0.138
51
HYP266 Hypoxia 55 0.136
52
c PRM023 Pre-Malignant Neoplasm 42 0.135
53
P APL001 Aplastic Anemia 74 0.135
54
c HMC010 Hemochromatosis, Type 3 38 0.135
55
CNG034 Congestive Heart Failure 72 0.132
56
P SDR003 Sideroblastic Anemia 40 0.130
57
c CHR089 Chronic Kidney Failure 67 0.126
58
HMT018 Hematopoietic Stem Cell Transplantation 39 0.125
59
END072 Endotheliitis 41 0.119
60
MTL002 Metal Metabolism Disorder 37 0.116
61
MTH009 Mouth Disease 63 0.116
62
P URF003 Urofacial Syndrome 1 51 0.115
63
P CRN178 Coronary Heart Disease 6 22 0.111
64
ALR002 Al-Raqad Syndrome 36 0.111
65
HMT002 Hematologic Cancer 62 0.111
66
P SCK034 Sickle Beta Thalassemia 33 0.110
67
LVR012 Liver Cirrhosis 71 0.110
68
c ACT073 Acute Leukemia 61 0.109
69
ADL002 Adult Syndrome 53 0.108
70
P CRD011 Cardiomyopathy 66 0.106
71
c HPT073 Hepatitis C Virus 72 0.106
72
TBR010 Tuberculosis 70 0.105
73
ACR006 Aceruloplasminemia 46 0.105
74
HRT007 Heart Cancer 51 0.105
75
P HRT017 Heart Tumor 34 0.105
76
c ADL079 Adult Heart Tumor 17 0.105
77
NNL002 Nonalcoholic Steatohepatitis 49 0.105
78
DDN006 Duodenitis 44 0.104
79
c CRN214 Coronary Heart Disease 5 22 0.104
80
CNG028 Congenital Hypoplastic Anemia 48 0.102
81
VTM003 Vitamin Metabolic Disorder 31 0.102
82
c HMG004 Hemoglobin D Disease 32 0.102
83
P OBS005 Obesity 91 0.101
84
RTN023 Retinitis 49 0.100
85
END030 End Stage Renal Failure 53 0.099
86
P ATX004 Ataxia 53 0.099
87
P MYL006 Myeloid Leukemia 67 0.097
88
c HMG001 Hemoglobin C Disease 46 0.097
89
CLC007 Calcium Metabolism Disease 39 0.097
90
RFR010 Refractory Anemia 43 0.097
91
P DMN001 Diamond-Blackfan Anemia 69 0.096
92
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.095
93
PNC034 Pancreas Disease 56 0.095
94
PLS009 Plasma Cell Neoplasm 47 0.095
95
c PNC106 Pancreatic Agenesis 1 31 0.095
96
c CRN172 Coronary Heart Disease 3 19 0.094
97
P ART022 Arthritis 73 0.093
98
PYR013 Pyruvate Kinase Deficiency 58 0.092
99
FTT001 Fatty Liver Disease 60 0.091
100
P LYM118 Lymphoma 68 0.090
101
c CRN175 Coronary Heart Disease 4 19 0.089
102
HRT029 Heart Tumor of the Child 16 0.089
103
P HRT032 Heart Disease 64 0.088
104
SNG003 Single Ventricular Heart 23 0.088
105
PRR002 Pure Red-Cell Aplasia 47 0.087
106
P KDN017 Kidney Cancer 67 0.085
107
P LYM026 Lymphoblastic Leukemia 60 0.085
108
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.085
109
HYP080 Hypogonadism 54 0.084
110
c CRN177 Coronary Heart Disease 7 21 0.084
111
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.084
112
P PLM037 Pulmonary Hypertension 78 0.083
113
PCK002 Pick Disease 66 0.082
114
c HMG003 Hemoglobin E Disease 44 0.082
115
BNC003 Bone Cancer 44 0.082
116
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 35 0.082
117
IMM127 Immune System Cancer 41 0.082
118
CHL071 Child Syndrome 58 0.081
119
KDS001 Kid Syndrome 53 0.081
120
BNS002 Bone Structure Disease 37 0.081
121
c CRN173 Coronary Heart Disease 8 19 0.081
122
ACT118 Acute Non Lymphoblastic Leukemia 27 0.080
123
BLD054 Blood Protein Disease 38 0.080
124
P HYP086 Hypothyroidism 63 0.080
125
CRB009 Cerebritis 36 0.080
126
P FRD001 Friedreich Ataxia 62 0.079
127
c LKM061 Leukemia, Acute Myeloid 71 0.078
128
c CHR064 Chronic Monocytic Leukemia 42 0.078
129
c CRN174 Coronary Heart Disease 2 19 0.078
130
P MYL005 Myelofibrosis 67 0.078
131
LYM024 Lymphatic System Disease 49 0.078
132
LYM023 Lymphatic System Cancer 35 0.078
133
P CTR002 Cataract 57 0.077
134
PRP027 Peripheral Vascular Disease 69 0.077
135
PLC008 Placenta Disease 33 0.076
136
P HYP060 Hyperinsulinism 58 0.076
137
LYM067 Lymphoid Leukemia 38 0.076
138
ADJ001 Adjustment Disorder 38 0.076
139
ISC004 Ischemia 56 0.076
140
PLS010 Plasma Protein Metabolism Disease 37 0.076
141
P MYL007 Myeloma 52 0.075
142
P CNG003 Congenital Dyserythropoietic Anemia 38 0.074
143
c DMN005 Diamond-Blackfan Anemia 2 22 0.074
144
c MLT019 Multiple Myeloma 77 0.073
145
ATR060 Atrial Standstill, Digenic 51 0.073
146
LYM019 Lymphosarcoma 52 0.073
147
ACR041 Acromelic Frontonasal Dysostosis 45 0.073
148
c VRL010 Viral Hepatitis 60 0.073
149
BRT030 Birth Defects 44 0.073
150
VSC008 Vascular Hemostatic Disease 30 0.073
151
c LKM062 Leukemia, Acute Lymphoblastic 63 0.072
152
c LYM107 Lymphoproliferative Syndrome 2 32 0.072
153
P ACT074 Acute Lymphocytic Leukemia 54 0.072
154
LYM040 Lymphoblastic Lymphoma 51 0.072
155
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 31 0.072
156
c LKM055 Leukemia, Acute Lymphoblastic 2 21 0.072
157
BNL002 Bone Lymphoma 34 0.072
158
c ADL052 Adult Acute Lymphocytic Leukemia 41 0.072
159
SYS003 Systolic Heart Failure 42 0.072
160
PRM151 Primary Bone Lymphoma 26 0.072
161
HYP099 Hyperferritinemia-Cataract Syndrome 43 0.072
162
P ACQ009 Acquired Metabolic Disease 42 0.071
163
c TRC078 Trichohepatoenteric Syndrome 2 30 0.071
164
c DMN023 Diamond-Blackfan Anemia 1 39 0.070
165
URN009 Urinary System Disease 52 0.070
166
P BLD051 Blood Coagulation Disease 44 0.070
167
ATH003 Atherosclerosis 63 0.070
168
VND001 Vein Disease 51 0.070
169
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.070
170
SPL012 Splenic Disease 48 0.070
171
MNR003 Mineral Metabolism Disease 39 0.068
172
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.068
173
P RTN016 Retinal Degeneration 50 0.068
174
c CHR092 Chronic Myeloproliferative Disease 50 0.068
175
MLN008 Melanoma 61 0.067
176
P HRD011 Hereditary Spherocytosis 51 0.066
177
P LCT001 Lactic Acidosis 52 0.066
178
P ADN016 Adenocarcinoma 69 0.066
179
ORL011 Oral Cancer 53 0.066
180
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.065
181
c LYM106 Lymphoproliferative Syndrome 1 33 0.065
182
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.065
183
WLS001 Wilson Disease 72 0.065
184
P NRB001 Neuroblastoma 70 0.065
185
ALN001 Aland Island Eye Disease 45 0.065
186
ADN018 Adenoma 59 0.065
187
P BRS047 Breast Cancer 100 0.065
188
GLT021 Glutaricaciduria, Type I 47 0.065
189
CSY001 C Syndrome 49 0.064
190
INC022 Inclusion-Cell Disease 46 0.064
191
VSC006 Vascular Cancer 51 0.064
192
PLS016 Plasma Cell Leukemia 52 0.064
193
RFR004 Refractory Hematologic Cancer 27 0.064
194
c HPT016 Hepatitis B 61 0.064
195
LNG099 Lung Disease 63 0.064
196
P SPS003 Spastic Diplegia 49 0.064
197
P ORL007 Oral Cavity Cancer 58 0.063
198
c DMN024 Diamond-Blackfan Anemia 7 28 0.063
199
AMN006 Aminoaciduria 39 0.063
200
HMG015 Hemoglobin S Beta-Thalassemia 16 0.063
201
c CHR418 Chronic Leukemia 48 0.062
202
PLS003 Plasmacytic Leukemia 22 0.062
203
c ADL001 Adult Lymphoma 40 0.062
204
c CHR096 Chronic Pulmonary Heart Disease 40 0.062
205
INT066 Interstitial Lung Disease 60 0.062
206
MSC004 Muscle Tissue Disease 35 0.062
207
P ENC018 Encephalopathy 59 0.062
208
ANG049 Angioedema Induced by Ace Inhibitors 35 0.062
209
INT253 Intestinal Benign Neoplasm 48 0.062
210
PRM025 Primary Bacterial Infectious Disease 42 0.060
211
SPL011 Spleen Cancer 38 0.060
212
BRN106 Burns 52 0.060
213
c SCK008 Sickle Delta Beta Thalassemia 9 0.060
214
HV1006 Hiv-1 80 0.060
215
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.060
216
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.060
217
LPD008 Lipid Metabolism Disorder 42 0.060
218
P MYC007 Myocardial Infarction 80 0.059
219
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.059
220
CNT098 Central Core Disease 68 0.058
221
c MTB001 Metabolic Syndrome X 61 0.058
222
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 36 0.058
223
EXF001 Exfoliation Syndrome 56 0.058
224
HPT074 Hepatic Adenoma, Somatic 35 0.058
225
WLL006 Wells Syndrome 57 0.058
226
P PLN008 Peeling Skin Syndrome 45 0.058
227
GDS001 Good Syndrome 46 0.058
228
P NRP001 Neuropathy 57 0.058
229
GLC008 Glucose Metabolism Disease 44 0.058
230
P OST002 Osteoporosis 63 0.058
231
FRB001 Farber Lipogranulomatosis 54 0.058
232
c FNC027 Fanconi Anemia, Complementation Group a 71 0.058
233
P FNC004 Fanconi Syndrome 54 0.058
234
MYL004 Myelodysplastic Myeloproliferative Cancer 46 0.058
235
P MLT074 Multiple Endocrine Neoplasia 55 0.058
236
c ACT020 Acute T Cell Leukemia 38 0.058
237
LVR006 Liver Lymphoma 29 0.058
238
CHL068 Cholestasis 57 0.057
239
P CRN211 Coronary Artery Disease 74 0.057
240
ANX002 Anxiety Disorder 67 0.057
241
c HMC035 Hemochromatosis, Type 4 38 0.057
242
GRW007 Growth Hormone Deficiency 49 0.057
243
P PNM006 Pneumoconiosis 51 0.057
244
c CHR090 Chronic Lymphocytic Leukemia 73 0.056
245
P OST012 Osteoarthritis 81 0.056
246
P INF032 Infertility 61 0.056
247
P ART023 Arthropathy 63 0.056
248
PRS047 Prostatitis 56 0.056
249
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 0.055
250
c DMN017 Diamond-Blackfan Anemia 10 28 0.055
251
c ACT071 Acute Kidney Failure 48 0.055
252
c DMN021 Diamond-Blackfan Anemia 6 26 0.055
253
ATN005 Autonomic Dysfunction 44 0.055
254
RNL025 Renal Hypoplasia 40 0.055
255
VSC001 Vascular Myelopathy 25 0.055
256
P CHR562 Chronic Myelocytic Leukemia 39 0.055
257
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 16 0.055
258
P PRS040 Prostate Cancer 89 0.054
259
PLM033 Pulmonary Embolism 59 0.054
260
LYM115 Lymphoma, Non-Hodgkin 64 0.054
261
P BCL006 B-Cell Lymphomas 64 0.054
262
END035 Endocrine Gland Cancer 50 0.054
263
c LKM004 Leukemia, B-Cell, Chronic 24 0.054
264
VSC018 Visceral Steatosis 37 0.054
265
c LKM050 Leukemia, Chronic Lymphocytic 1 21 0.054
266
c LKM051 Leukemia, Chronic Lymphocytic 3 21 0.054
267
HPT067 Hepatocellular Adenoma 41 0.054
268
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.054
269
PHY002 Physical Disorder 43 0.054
270
P HYP024 Hypoparathyroidism 52 0.052
271
P RNL015 Renal Hypertension 47 0.052
272
ART111 Artery Disease 56 0.052
273
BRN071 Brain Injury 51 0.052
274
P MDL005 Medulloblastoma 76 0.052
275
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.052
276
ATN002 Autonomic Nervous System Disease 46 0.052
277
MNT001 Mantle Cell Lymphoma 72 0.052
278
P NRV006 Nervous System Cancer 62 0.052
279
c FLL041 Follicular Lymphoma 1 45 0.052
280
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.052
281
P FLL037 Follicular Lymphoma 68 0.052
282
PTT009 Pituitary Gland Disease 45 0.052
283
P CTN015 Cutaneous T Cell Lymphoma 41 0.052
284
P MYC008 Myocarditis 56 0.052
285
P ALC004 Alcohol Abuse 57 0.052
286
ANR040 Aneurysm 56 0.052
287
LKC003 Leukocyte Disease 45 0.052
288
SPL004 Splenic Marginal Zone Lymphoma 43 0.052
289
GND003 Gonadal Disease 41 0.052
290
c LKM056 Leukemia, Chronic Lymphocytic 2 40 0.052
291
ANX004 Anoxia 45 0.052
292
CHL061 Childhood Leukemia 47 0.052
293
CLL014 Cll/sll 42 0.052
294
RFR001 Refractory Plasma Cell Neoplasm 17 0.052
295
MRG003 Marginal Zone B-Cell Lymphoma 50 0.052
296
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.052
297
c CLL013 Cell Type Cancer 46 0.052
298
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 30 0.052
299
VSC047 Vascular Malformation 45 0.052
300
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 36 0.052
301
RSP006 Respiratory System Disease 61 0.050
302
P TRC086 Trichohepatoenteric Syndrome 1 46 0.050
303
OCL009 Ocular Cancer 61 0.050
304
P ESP024 Esophagitis 62 0.050
305
c PLN021 Peeling Skin Syndrome 3 30 0.050
306
AYM001 Ayme-Gripp Syndrome 40 0.050
307
P MSC033 Muscle Disorders 52 0.050
308
P OVR042 Ovarian Cancer 73 0.049
309
HDG012 Hodgkin Lymphoma 75 0.049
310
EWN003 Ewing Sarcoma 63 0.049
311
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.049
312
WST001 West Syndrome 61 0.049
313
BRK010 Burkitt Lymphoma 66 0.049
314
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 29 0.049
315
MYC006 Mycosis Fungoides 66 0.049
316
TST021 Testicular Germ Cell Tumor 67 0.049
317
BLR008 Bilirubin Metabolic Disorder 46 0.049
318
P HYP117 Hypertriglyceridemia 65 0.049
319
MSS002 Mass Syndrome 49 0.049
320
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.049
321
SZR001 Sezary's Disease 51 0.049
322
c ADL017 Adult T-Cell Leukemia 59 0.049
323
HDG004 Hodgkin's Granuloma 25 0.049
324
P OVR049 Ovarian Disease 54 0.049
325
MNG003 Mungan Syndrome 21 0.049
326
RTC005 Reticulosarcoma 46 0.049
327
RTC009 Reticulum Cell Sarcoma 46 0.049
328
DFF005 Diffuse Large B-Cell Lymphoma 57 0.049
329
MXD023 Mixed Cell Type Cancer 45 0.049
330
HDG006 Hodgkin's Paragranuloma 18 0.049
331
HFS001 Hfe-Associated Hereditary Hemochromatosis 28 0.049
332
PLS025 Plasmablastic Lymphoma 46 0.049
333
HML018 Homologous Wasting Disease 14 0.049
334
GRM001 Germ Cell and Embryonal Cancer 38 0.049
335
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 27 0.049
336
P TCL004 T-Cell Leukemia 44 0.049
337
c LKM005 Leukemia, T-Cell, Chronic 21 0.049
338
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 19 0.049
339
c CRN176 Coronary Heart Disease 9 19 0.049
340
PRM128 Primary Cutaneous Follicle Center Lymphoma 25 0.049
341
LYM048 Lymphoma, Large-Cell, Immunoblastic 19 0.049
342
BND002 B- and T-Cell Mixed Leukemia 18 0.049
343
END038 Endocrine Pancreas Disease 42 0.049
344
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.049
345
ARG006 Aregenerative Anemia 21 0.049
346
P MSC007 Muscle Hypertrophy 55 0.049
347
P PNC035 Pancreatic Cancer 86 0.048
348
c HMC021 Hemochromatosis, Type 2a 29 0.048
349
P ADL010 Adult Respiratory Distress Syndrome 60 0.048
350
P ESN007 Eosinophilia 61 0.048
351
LRN003 Learning Disability 49 0.048
352
ZYG002 Zygomycosis 33 0.048
353
FML039 Female Reproductive System Disease 49 0.048
354
P LTR001 Lateral Sclerosis 50 0.048
355
BRN004 Brain Edema 51 0.048
356
c MLT136 Multiple Endocrine Neoplasia 1 68 0.046
357
TST014 Testicular Cancer 55 0.046
358
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 40 0.046
359
TST015 Testicular Disease 47 0.046
360
ABL002 Ablepharon-Macrostomia Syndrome 51 0.046
361
EPS006 Epstein Syndrome 40 0.046
362
P ACT117 Acute Myelomonocytic Leukemia 46 0.046
363
c DMN006 Diamond-Blackfan Anemia 3 29 0.046
364
P HRT035 Heart Block, Congenital 40 0.046
365
c NRB015 Neuroblastoma 2 31 0.046
366
c CHR285 Chronic Myelomonocytic Leukemia 54 0.046
367
c DMN022 Diamond-Blackfan Anemia 9 25 0.046
368
c DMN020 Diamond-Blackfan Anemia 8 26 0.046
369
DFF027 Diffuse Lymphatic Malformation 28 0.046
370
GLM004 Gliomatosis Cerebri 48 0.046
371
OVR094 Ovarian Epithelial Cancer 48 0.046
372
URM002 Uremia 36 0.046
373
c CHR417 Chronic Graft Versus Host Disease 50 0.046
374
LYM127 Lymphatic Malformations 38 0.046
375
PRP036 Peripheral T-Cell Lymphoma 44 0.046
376
DST006 Diastolic Heart Failure 45 0.046
377
BNP001 Bone Peripheral Neuroepithelioma 17 0.046
378
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 39 0.046
379
c NRB013 Neuroblastoma 6 19 0.046
380
BRS001 Breast Lymphoma 31 0.046
381
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 24 0.046
382
TST004 Testicular Lymphoma 34 0.046
383
c PRM200 Primary Fanconi Syndrome 24 0.046
384
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 16 0.046
385
c FNC011 Fanconi Like Syndrome 18 0.046
386
OVR021 Ovarian Lymphoma 33 0.046
387
OVR056 Ovarian Primitive Germ Cell Tumor 29 0.046
388
TST003 Testicular Leukemia 32 0.046
389
OVR069 Ovarian Germ Cell Tumor 21 0.046
390
VBR003 Vibrio Vulnificus Infection 23 0.046
391
c PLN018 Peeling Skin Syndrome 2 36 0.046
392
ALL026 Allergic Hypersensitivity Disease 53 0.046
393
HMC038 Hemochromatosis, Neonatal 27 0.046
394
c HPT003 Hepatitis a 55 0.046
395
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 35 0.046
396
c PLN017 Peeling Skin Syndrome 1 32 0.046
397
P PNC001 Pancytopenia 53 0.046
398
P EPL164 Epilepsy 60 0.046
399
ALC006 Alcoholic Hepatitis 60 0.046
400
c DLT001 Delta Chain Disease 14 0.046
401
P LFR001 Li-Fraumeni Syndrome 79 0.044
402
ART016 Aortic Aneurysm 67 0.044
403
INT007 Intermediate Coronary Syndrome 52 0.044
404
STR026 Star Syndrome 57 0.044
405
C3D001 C3 Deficiency 50 0.044
406
ETN001 Eating Disorder 59 0.044
407
P MMB011 Membranous Nephropathy 53 0.044
408
P ABD003 Abdominal Aortic Aneurysm 43 0.044
409
THY030 Thyroid Gland Disease 52 0.044
410
ANT018 Anthracosis 41 0.044
411
BRS051 Breast Disease 57 0.044
412
LPD027 Lip Disease 35 0.044
413
MCR004 Macroglobulinemia 48 0.044
414
P GNR027 Generalized Peeling Skin Syndrome 21 0.044
415
GTR002 Goiter 54 0.043
416
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 33 0.043
417
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 25 0.043
418
P TYR004 Tyrosinemia 44 0.043
419
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.043
420
SPN331 Spondyloocular Syndrome 27 0.043
421
END003 Endometrial Stromal Nodule 24 0.043
422
ATY004 Atypical Neurofibroma 31 0.043
423
ATH010 Athyreosis 31 0.043
424
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 35 0.041
425
ATR002 Atransferrinemia 48 0.041
426
INT271 Interstitial Lung and Liver Disease 32 0.041
427
NSD001 Nose Disease 51 0.041
428
c SVR001 Severe Acute Respiratory Syndrome 56 0.041
429
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 32 0.041
430
P HST010 Histiocytosis 56 0.041
431
PLM010 Pulmonary Edema 56 0.041
432
P LPC002 Lip Cancer 50 0.041
433
MXD005 Mixed Connective Tissue Disease 63 0.041
434
CNN005 Connective Tissue Disease 60 0.041
435
PLS011 Plasmacytoma 57 0.041
436
SXL003 Sexual Disorder 45 0.041
437
FML038 Female Reproductive Organ Cancer 50 0.041
438
OCL006 Ocular Hypertension 47 0.041
439
JNT002 Joint Disorders 55 0.041
440
BLD053 Blood Platelet Disease 44 0.041
441
FML037 Female Breast Cancer 49 0.041
442
ANP010 Anaplastic Plasmacytoma 21 0.041
443
CLN015 Colon Adenocarcinoma 55 0.041
444
P DYS021 Dysautonomia 47 0.041
445
CRN030 Coronary Stenosis 50 0.041
446
GRN017 Granulocytopenia 39 0.041
447
c EYL003 Eye Lymphoma 33 0.041
448
c DYS033 Dysautonomia Like Disorder 18 0.041
449
THY028 Thyroid Cancer 71 0.038
450
ALC007 Alcohol Dependence 66 0.038
451
THL016 Thalassemias, Alpha- 55 0.038
452
P PLR004 Pleuropulmonary Blastoma 63 0.038
453
VRL011 Viral Infectious Disease 56 0.038
454
MST006 Mast Syndrome 44 0.038
455
CHR066 Chronic Fatigue Syndrome 63 0.038
456
P SML016 Small Intestine Cancer 54 0.038
457
HRY003 Hairy Cell Leukemia 56 0.038
458
c HPT015 Hepatitis D 51 0.038
459
P WLD002 Waldenstrom Macroglobulinemia 62 0.038
460
P ANP001 Anaplastic Large Cell Lymphoma 58 0.038
461
ACR002 Acrocapitofemoral Dysplasia 35 0.038
462
NTR003 Natural Killer Cell Leukemia 46 0.038
463
TTH006 Tooth Disease 52 0.038
464
RPR002 Reproductive System Disease 45 0.038
465
P HYP069 Hyperparathyroidism 57 0.038
466
MST017 Mast Cell Disease 52 0.038
467
c DMN019 Diamond-Blackfan Anemia 4 29 0.038
468
MYC002 Mycobacterium Avium Complex Disease 52 0.038
469
MLR006 Male Reproductive Organ Cancer 46 0.038
470
MST002 Mast-Cell Leukemia 50 0.038
471
c MCR161 Macroglobulinemia, Waldenstrom 1 28 0.038
472
ANG046 Angioimmunoblastic T-Cell Lymphoma 42 0.038
473
HPT046 Hepatic Veno-Occlusive Disease 46 0.038
474
LYM012 Lymphoplasmacytic Lymphoma 46 0.038
475
ACQ016 Acquired Pure Red Cell Aplasia 25 0.038
476
MLR007 Male Reproductive System Disease 36 0.038
477
BRN002 Bronchiolitis 56 0.038
478
LYM051 Lymphomatoid Granulomatosis 46 0.038
479
MST004 Mast Cell Neoplasm 40 0.038
480
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 22 0.038
481
P ACT135 Acute Graft Versus Host Disease 52 0.038
482
c HMN021 Human T-Cell Leukemia Virus Type 1 51 0.038
483
PST046 Post-Transplant Lymphoproliferative Disease 53 0.038
484
SPC003 Specific Developmental Disorder 39 0.038
485
GLB003 Globe Disease 34 0.038
486
RNL097 Renal Artery Disease 44 0.038
487
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 41 0.038
488
SLT001 Solitary Osseous Plasmacytoma 38 0.038
489
SXD001 Sex Differentiation Disease 39 0.038
490
CTN011 Cutaneous Porphyria 29 0.038
491
MLG026 Male Genital Organ Vascular Disease 16 0.038
492
PTT037 Pituitary Tumors 45 0.038
493
PRP080 Peripheral Artery Disease 35 0.038
494
c MCR162 Macroglobulinemia, Waldenstrom 2 19 0.038
495
RNL021 Renal Tubular Transport Disease 35 0.038
496
HRY001 Hairy Cell Leukemia of Spleen 17 0.038
497
RFR002 Refractory Hairy Cell Leukemia 31 0.038
498
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.038
499
c ANP011 Anaplastic Small Cell Lymphoma 16 0.038
500
BND014 Bone Development Disease 40 0.038
501
PRM026 Primary Systemic Mycosis 40 0.038
502
PRM165 Primary Plasmacytoma of the Bone 14 0.038
503
LPN002 Lip and Oral Cavity Cancer 16 0.038
504
RNL077 Renal Fibrosis 48 0.038
505
P LNG028 Long Qt Syndrome 67 0.038
506
ADP002 Adiponectin Deficiency 30 0.038
507
BLN006 Blind Loop Syndrome 29 0.038
508
P SCH015 Schizophrenia 78 0.035
509
SKN016 Skin Disease 69 0.035
510
CYS036 Cystinosis, Nephropathic 40 0.035
511
P CMR001 Camurati-Engelmann Disease 63 0.035
512
MSS001 Masa Syndrome 49 0.035
513
c SRC025 Sarcoidosis 1 58 0.035
514
LNG024 Langerhans-Cell Histiocytosis 64 0.035
515
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 50 0.035
516
HND003 Hand-Foot-Uterus Syndrome 46 0.035
517
JNS003 Jensen Syndrome 33 0.035
518
ADR038 Adermatoglyphia 39 0.035
519
HYD046 Hydatidiform Mole, Recurrent, 1 41 0.035
520
TMR010 Tumor Predisposition Syndrome 58 0.035
521
PNC092 Pancreatic Agenesis and Congenital Heart Defects 27 0.035
522
P OVR075 Ovarian Dysgenesis 1 33 0.035
523
c MLT086 Multiple Endocrine Neoplasia, Type Iv 49 0.035
524
OLV001 Olivopontocerebellar Atrophy 53 0.035
525
P MST009 Mastocytosis 54 0.035
526
c OVR076 Ovarian Dysgenesis 2 32 0.035
527
SBS006 Sebastian Syndrome 36 0.035
528
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.035
529
c SYS004 Systemic Mastocytosis 60 0.035
530
GST010 Gestational Trophoblastic Neoplasm 40 0.035
531
c MTR002 Mitral Valve Insufficiency 42 0.035
532
P BRN009 Burning Mouth Syndrome 54 0.035
533
P HYP098 Hypereosinophilic Syndrome 48 0.035
534
P ART018 Aortic Valve Insufficiency 38 0.035
535
c NRB014 Neuroblastoma 3 29 0.035
536
c DMN018 Diamond-Blackfan Anemia 5 29 0.035
537
P ENC004 Encephalitis 60 0.035
538
TTH002 Tooth Agenesis 54 0.035
539
c PNC105 Pancreatic Agenesis 2 22 0.035
540
c PNC111 Pancreatic Cancer 2 33 0.035
541
c PNC094 Pancreatic Cancer 1 27 0.035
542
c DMN028 Diamond-Blackfan Anemia 12 27 0.035
543
NSY001 N Syndrome 42 0.035
544
P GND004 Gonadal Dysgenesis 51 0.035
545
HRZ001 Huriez Syndrome 33 0.035
546
P MSC003 Muscular Atrophy 51 0.035
547
P APL006 Aplasia Cutis Congenita 48 0.035
548
c OVR102 Ovarian Dysgenesis 3 24 0.035
549
DFF001 Diffuse Cutaneous Mastocytosis 42 0.035
550
CTN014 Cutaneous Mastocytosis 49 0.035
551
SBS003 Substance Abuse 54 0.035
552
SCK020 Sickle Cell - Hemoglobin D Disease 23 0.035
553
PRC013 Pericarditis 52 0.035
554
HPT014 Hepatorenal Syndrome 47 0.035
555
MCH010 Michels Syndrome 24 0.035
556
TRP005 Trophoblastic Neoplasm 33 0.035
557
MSC072 Muscle Cancer 47 0.035
558
VGN023 Vaginitis 41 0.035
559
CHR286 Chronic Neutrophilic Leukemia 44 0.035
560
LTT002 Letterer-Siwe Disease 32 0.035
561
PTT006 Pituitary Adenoma 54 0.035
562
CVT001 Cavitary Optic Disc Anomalies 25 0.035
563
PTT008 Pituitary Carcinoma 45 0.035
564
ACT103 Acute Lymphoblastic Leukemia, Childhood 22 0.035
565
HYP037 Hyperhomocysteinemia 49 0.035
566
c MYL058 Myeloproliferative Syndrome, Transient 23 0.035
567
PLM012 Pulmonary Sarcoidosis 54 0.035
568
c SBC004 Subacute Myeloid Leukemia 34 0.035
569
c CNN010 Connective Tissue Benign Neoplasm 31 0.035
570
NNF001 Non-Functioning Pancreatic Endocrine Tumor 38 0.035
571
VSC009 Vascular Skin Disease 21 0.035
572
P CNN004 Connective Tissue Cancer 44 0.035
573
INT054 Intraocular Lymphoma 46 0.035
574
BNN003 Bone Inflammation Disease 46 0.035
575
GST059 Gestational Trophoblastic Tumor 27 0.035
576
NRR001 Neuroretinitis 41 0.035
577
MXD025 Mixed Germ Cell Cancer 32 0.035
578
P TST026 Testicular Germ Cell Cancer 41 0.035
579
HRT012 Heart Valve Disease 39 0.035
580
P PNC045 Pancreatic Agenesis 44 0.035
581
MYC003 Myocardium Cancer 16 0.035
582
CHR563 Chronic Eosinophilic Leukemia 46 0.035
583
TND003 Toni-Debre-Fanconi Syndrome 16 0.035
584
c HMN022 Human T-Cell Leukemia Virus Type 2 45 0.035
585
OVR015 Ovarian Mixed Germ Cell Neoplasm 17 0.035
586
P MXD016 Mixed Gonadal Dysgenesis 35 0.035
587
UND007 Undifferentiated Connective Tissue Disease 27 0.035
588
CHR008 Choroiditis 43 0.035
589
c PRM149 Primary Hypereosinophilic Syndrome 39 0.035
590
c NRB012 Neuroblastoma 5 20 0.035
591
NRC007 Neuroectodermal Endocrine Syndrome 20 0.035
592
LNG013 Lung Lymphoma 40 0.035
593
LYM117 Lymphocytic Hypereosinophilic Syndrome 15 0.035
594
c HMN023 Human T-Cell Leukemia Virus Type 3 15 0.035
595
HRT003 Heart Lymphoma 31 0.035
596
PTT001 Pituitary Hypoplasia 29 0.035
597
c SCN042 Secondary Hypereosinophilic Syndrome 15 0.035
598
HPT070 Hepatosplenic T-Cell Lymphoma 40 0.035
599
PDT001 Pediatric Lymphoma 39 0.035
600
PNL011 Pineal Region Germinoma 18 0.035
601
MLG035 Malignant Ovarian Mixed Epithelial Neoplasm 14 0.035
602
MXD024 Mixed Epithelial Tumor of Ovary 15 0.035
603
SML008 Small Intestine Lymphoma 43 0.035
604
c TST017 Testicular Malignant Germ Cell Cancer 22 0.035
605
CRT057 Critical Congenital Heart Disease 19 0.035
606
ADL082 Adult Pulmonary Langerhans Cell Histiocytosis 21 0.035
607
MTL005 Metal Allergy 34 0.035
608
c SML023 Small Cell Lung Cancer, Adult 17 0.035
609
WSC001 Wisconsin Syndrome 16 0.035
610
PRM133 Primary Pulmonary Lymphoma 24 0.035
611
TST040 Testicular Trophoblastic Tumor 21 0.035
612
c ATM022 Autoimmune Myocarditis 39 0.035
613
DSS003 Disseminated Eosinophilic Collagen Disease 17 0.035
614
HPD002 Hepadnavirus Infection 20 0.035
615
ISL032 Isolated Bone Marrow Mastocytosis 16 0.035
616
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 15 0.035
617
P ORG009 Organ System Cancer 45 0.035
618
MLG088 Malignant Germ Cell Tumor 27 0.035
619
MXD032 Mixed Germ Cell Tumor 31 0.035
620
FNC012 Functioning Pancreatic Endocrine Tumor 14 0.035
621
HDG010 Hodgkin Lymphoma, During Pregnancy 13 0.035
622
NNH004 Non-Hodgkin Lymphoma, During Pregnancy 13 0.035
623
PRP032 Porphyria Variegata 51 0.030
624
DBN001 Dubin-Johnson Syndrome 52 0.030
625
CRT002 Cartilage-Hair Hypoplasia 57 0.030
626
P HYP061 Hypertrophic Cardiomyopathy 64 0.030
627
PRP019 Peripheral Nervous System Disease 52 0.030
628
P GT001 Gout 58 0.030
629
SPT004 Septic Arthritis 60 0.030
630
LST001 Listeriosis 53 0.030
631
P MTR012 Mitral Valve Disease 59 0.030
632
ADN001 Adenosine Deaminase Deficiency 45 0.030
633
c ATM011 Autoimmune Hepatitis 62 0.030
634
P STM009 Stomatocytosis I 20 0.030
635
HYP005 Hypokalemia 52 0.030
636
HPT022 Hepatoblastoma 57 0.030
637
WRF003 Warfarin Syndrome 30 0.030
638
RNL011 Renal Osteodystrophy 48 0.030
639
PRC012 Pericardial Effusion 50 0.030
640
P GLM007 Glomerulonephritis 56 0.030
641
ISC006 Ischemic Heart Disease 54 0.030
642
CRD001 Cardiac Tamponade 43 0.030
643
PRR013 Prurigo Nodularis 37 0.030
644
HPT009 Hepatopulmonary Syndrome 48 0.030
645
MMB002 Membranous Glomerulonephritis 47 0.030
646
RHS001 Rh Isoimmunization 27 0.030
647
XLN067 X-Linked Protoporphyria 19 0.030
648
c TFR001 Tfr2-Related Hereditary Hemochromatosis 13 0.030
649
CMP052 Complication in Hemodialysis 14 0.030