Search results for "iron overload"

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

648 hits were found for 'iron overload'

# Family MCID Name MIFTS Score
1
IRN008 Iron Overload in Africa 31 7.793
2
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 14 7.719
3
c HMC034 Hemochromatosis, Type 5 30 7.224
4
c ANM027 Anemia, Hypochromic Microcytic, with Iron Overload 2 19 6.256
5
GRC001 Gracile Syndrome 33 5.155
6
ANM030 Anemia, Hypochromic Microcytic 36 5.152
7
HMS001 Hemosiderosis 46 4.212
8
c HMC009 Hemochromatosis Type 2 39 2.602
9
GNT037 Genetic Hyperferritinemia Without Iron Overload 5 2.594
10
FRR002 Ferro-Cerebro-Cutaneous Syndrome 9 2.564
11
ZLL001 Zellweger Syndrome 56 2.539
12
DFC004 Deficiency Anemia 64 0.577
13
IRN001 Iron Deficiency Anemia 52 0.448
14
P HMC003 Hemochromatosis 72 0.443
15
IRN002 Iron Metabolism Disease 41 0.439
16
P THL005 Thalassemia 64 0.395
17
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.321
18
P HPT021 Hepatitis 69 0.321
19
NTR005 Nutritional Deficiency Disease 36 0.275
20
THL018 Thalassemia Major 48 0.270
21
LPD004 Lipoid Nephrosis 48 0.252
22
HMG005 Hemoglobinopathy 52 0.217
23
THL017 Thalassemia Intermedia 40 0.216
24
P HML002 Hemolytic Anemia 62 0.216
25
THL010 Thalassemia Minor 39 0.211
26
c CNG027 Congenital Hemolytic Anemia 48 0.208
27
MYL009 Myelodysplastic Syndrome 73 0.201
28
P HPT023 Hepatocellular Carcinoma 92 0.194
29
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.191
30
SCK003 Sickle Cell Anemia 71 0.182
31
SCK005 Sickle Cell Disease 51 0.181
32
c HPT001 Hepatitis C 68 0.181
33
P LVR013 Liver Disease 75 0.175
34
P SDR002 Siderosis 44 0.169
35
MRG013 Mirage Syndrome 29 0.164
36
P KDN018 Kidney Disease 66 0.162
37
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.153
38
P PRP029 Porphyria 59 0.152
39
BNM001 Bone Marrow Cancer 51 0.152
40
P LKM002 Leukemia 71 0.148
41
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.147
42
P HRT032 Heart Disease 75 0.147
43
CNG034 Congestive Heart Failure 72 0.146
44
IMP003 Impaired Renal Function Disease 34 0.144
45
P PRP003 Porphyria Cutanea Tarda 64 0.144
46
NRN002 Neuronitis 41 0.144
47
P APL001 Aplastic Anemia 75 0.141
48
MCR018 Microcytic Anemia 43 0.138
49
c INH020 Inherited Metabolic Disorder 49 0.138
50
c PRM023 Pre-Malignant Neoplasm 41 0.138
51
HYP266 Hypoxia 56 0.137
52
c HMC010 Hemochromatosis, Type 3 39 0.135
53
c CHR089 Chronic Kidney Failure 66 0.133
54
P SDR003 Sideroblastic Anemia 40 0.129
55
HMT018 Hematopoietic Stem Cell Transplantation 41 0.127
56
PRM243 Primary Bone Cancer 29 0.126
57
NNL002 Nonalcoholic Steatohepatitis 50 0.120
58
P CRD011 Cardiomyopathy 68 0.120
59
END072 Endotheliitis 42 0.119
60
c ACT073 Acute Leukemia 60 0.117
61
P SCK034 Sickle Beta Thalassemia 30 0.116
62
MTL002 Metal Metabolism Disorder 35 0.115
63
c CRN214 Coronary Heart Disease 5 22 0.113
64
MTH009 Mouth Disease 61 0.113
65
c HMG001 Hemoglobin C Disease 47 0.113
66
LVR012 Liver Cirrhosis 67 0.113
67
c HPT073 Hepatitis C Virus 73 0.112
68
HRT007 Heart Cancer 46 0.111
69
P HRT017 Heart Tumor 32 0.111
70
c ADL079 Adult Heart Tumor 16 0.111
71
c HMG004 Hemoglobin D Disease 31 0.110
72
VTM003 Vitamin Metabolic Disorder 30 0.108
73
ACR006 Aceruloplasminemia 45 0.108
74
URN009 Urinary System Disease 50 0.106
75
P URF003 Urofacial Syndrome 1 50 0.106
76
P CRN178 Coronary Heart Disease 6 21 0.105
77
PNC034 Pancreas Disease 58 0.104
78
c PNC106 Pancreatic Agenesis 1 37 0.104
79
CNG028 Congenital Hypoplastic Anemia 48 0.104
80
DDN006 Duodenitis 42 0.103
81
END030 End Stage Renal Failure 55 0.103
82
HMT002 Hematologic Cancer 64 0.103
83
c CRN172 Coronary Heart Disease 3 19 0.102
84
P OBS005 Obesity 92 0.102
85
RTN023 Retinitis 50 0.102
86
P ATX004 Ataxia 53 0.101
87
P MYL006 Myeloid Leukemia 66 0.100
88
RFR010 Refractory Anemia 45 0.099
89
PLS009 Plasma Cell Neoplasm 48 0.099
90
TBR010 Tuberculosis 70 0.098
91
ACD009 Acid-Labile Subunit, Deficiency of 45 0.098
92
P DMN001 Diamond-Blackfan Anemia 69 0.098
93
HRT029 Heart Tumor of the Child 15 0.096
94
P LYM026 Lymphoblastic Leukemia 62 0.095
95
P LYM033 Lymphoproliferative Syndrome 56 0.095
96
ADL002 Adult Syndrome 52 0.094
97
ALR002 Al-Raqad Syndrome 36 0.094
98
P ART022 Arthritis 75 0.093
99
PYR013 Pyruvate Kinase Deficiency 58 0.093
100
FTT001 Fatty Liver Disease 59 0.092
101
c HMG003 Hemoglobin E Disease 44 0.091
102
PRR002 Pure Red-Cell Aplasia 47 0.089
103
SNG003 Single Ventricular Heart 22 0.089
104
ISC004 Ischemia 61 0.088
105
LYM024 Lymphatic System Disease 52 0.088
106
P LYM118 Lymphoma 69 0.088
107
P CNG003 Congenital Dyserythropoietic Anemia 40 0.088
108
P KDN017 Kidney Cancer 65 0.087
109
LYM067 Lymphoid Leukemia 44 0.087
110
c CRN177 Coronary Heart Disease 7 20 0.087
111
PRP027 Peripheral Vascular Disease 69 0.087
112
BLD054 Blood Protein Disease 37 0.086
113
P PLM037 Pulmonary Hypertension 79 0.086
114
c CRN173 Coronary Heart Disease 8 18 0.085
115
SYS003 Systolic Heart Failure 43 0.084
116
ADJ001 Adjustment Disorder 38 0.084
117
ACT118 Acute Non Lymphoblastic Leukemia 30 0.084
118
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.084
119
HYP080 Hypogonadism 53 0.083
120
LYM023 Lymphatic System Cancer 33 0.083
121
ANM029 Anemia, Sideroblastic, X-Linked 48 0.083
122
c LKM062 Leukemia, Acute Lymphoblastic 64 0.082
123
P ACT074 Acute Lymphocytic Leukemia 56 0.082
124
LYM040 Lymphoblastic Lymphoma 53 0.082
125
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.082
126
c CHR064 Chronic Monocytic Leukemia 42 0.082
127
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.082
128
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.082
129
PLS010 Plasma Protein Metabolism Disease 34 0.082
130
P MYL005 Myelofibrosis 67 0.081
131
P FRD001 Friedreich Ataxia 62 0.081
132
c LKM061 Leukemia, Acute Myeloid 73 0.080
133
P HYP086 Hypothyroidism 64 0.080
134
ATR060 Atrial Standstill, Digenic 51 0.080
135
BRT030 Birth Defects 43 0.080
136
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.080
137
GLT021 Glutaricaciduria, Type I 46 0.079
138
PLC008 Placenta Disease 33 0.079
139
P MLT019 Multiple Myeloma 83 0.078
140
CRB009 Cerebritis 39 0.078
141
c CRN175 Coronary Heart Disease 4 19 0.078
142
c VRL010 Viral Hepatitis 60 0.078
143
P SPS003 Spastic Diplegia 52 0.078
144
VSC008 Vascular Hemostatic Disease 30 0.078
145
P CTR002 Cataract 58 0.077
146
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.077
147
c ADL001 Adult Lymphoma 39 0.077
148
PCK002 Pick Disease 68 0.077
149
P HMR003 Hemorrhagic Disease 57 0.076
150
c CRN174 Coronary Heart Disease 2 20 0.076
151
P HYP060 Hyperinsulinism 58 0.076
152
c LYM107 Lymphoproliferative Syndrome 2 50 0.076
153
BNL002 Bone Lymphoma 32 0.076
154
PRM151 Primary Bone Lymphoma 26 0.076
155
c DMN005 Diamond-Blackfan Anemia 2 22 0.076
156
SPL012 Splenic Disease 46 0.075
157
P BLD051 Blood Coagulation Disease 42 0.075
158
c TRC078 Trichohepatoenteric Syndrome 2 29 0.074
159
P NRB001 Neuroblastoma 70 0.073
160
CHL071 Child Syndrome 58 0.073
161
KDS001 Kid Syndrome 53 0.073
162
VND001 Vein Disease 47 0.072
163
c DMN023 Diamond-Blackfan Anemia 1 38 0.072
164
LPD008 Lipid Metabolism Disorder 58 0.072
165
P RTN016 Retinal Degeneration 54 0.072
166
LYM019 Lymphosarcoma 53 0.072
167
MYL031 Myeloproliferative Neoplasm 58 0.072
168
c ACT020 Acute T Cell Leukemia 35 0.072
169
c HMC035 Hemochromatosis, Type 4 39 0.071
170
HYP099 Hyperferritinemia-Cataract Syndrome 42 0.071
171
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.070
172
VSC006 Vascular Cancer 51 0.070
173
PLS016 Plasma Cell Leukemia 42 0.070
174
RFR004 Refractory Hematologic Cancer 28 0.070
175
c LKM060 Leukemia, Acute Lymphoblastic 3 50 0.070
176
P ACQ009 Acquired Metabolic Disease 38 0.070
177
c LYM106 Lymphoproliferative Syndrome 1 32 0.070
178
MLN008 Melanoma 62 0.069
179
ALL026 Allergic Hypersensitivity Disease 52 0.069
180
P ENC018 Encephalopathy 59 0.069
181
MSC004 Muscle Tissue Disease 34 0.069
182
CSY001 C Syndrome 50 0.068
183
c CHR418 Chronic Leukemia 47 0.068
184
INC022 Inclusion-Cell Disease 46 0.068
185
CRD118 Cardiovascular Cancer 44 0.068
186
c CHR096 Chronic Pulmonary Heart Disease 40 0.068
187
PLS003 Plasmacytic Leukemia 21 0.068
188
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.068
189
LVR006 Liver Lymphoma 27 0.068
190
ATH003 Atherosclerosis 65 0.067
191
INT253 Intestinal Benign Neoplasm 47 0.067
192
WLS001 Wilson Disease 72 0.067
193
ACR041 Acromelic Frontonasal Dysostosis 45 0.067
194
P HRD011 Hereditary Spherocytosis 54 0.066
195
SPL011 Spleen Cancer 36 0.066
196
THR024 Thrombosis 57 0.066
197
ANG049 Angioedema Induced by Ace Inhibitors 34 0.066
198
c HPT016 Hepatitis B 65 0.066
199
c DMN024 Diamond-Blackfan Anemia 7 28 0.066
200
P BRS047 Breast Cancer 100 0.065
201
P ADN016 Adenocarcinoma 69 0.065
202
CRB025 Carbohydrate Metabolic Disorder 46 0.065
203
MNR003 Mineral Metabolism Disease 38 0.065
204
WLL006 Wells Syndrome 59 0.064
205
ADN018 Adenoma 58 0.064
206
GDS001 Good Syndrome 44 0.064
207
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.064
208
PRM025 Primary Bacterial Infectious Disease 41 0.064
209
AMN006 Aminoaciduria 41 0.063
210
HMG015 Hemoglobin S Beta-Thalassemia 14 0.063
211
BRN106 Burns 52 0.063
212
P LCT001 Lactic Acidosis 51 0.063
213
VSC047 Vascular Malformation 45 0.063
214
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.063
215
c SCK008 Sickle Delta Beta Thalassemia 9 0.063
216
c CHR090 Chronic Lymphocytic Leukemia 76 0.062
217
P INF032 Infertility 59 0.062
218
EXF001 Exfoliation Syndrome 57 0.062
219
P PLN008 Peeling Skin Syndrome 45 0.062
220
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.062
221
GRW007 Growth Hormone Deficiency 50 0.062
222
ALN001 Aland Island Eye Disease 45 0.062
223
P MYC007 Myocardial Infarction 79 0.061
224
ACT058 Active Peptic Ulcer Disease 43 0.061
225
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.061
226
CHL068 Cholestasis 59 0.061
227
P PNC035 Pancreatic Cancer 87 0.060
228
P BCL006 B-Cell Lymphomas 65 0.060
229
CNT098 Central Core Disease 65 0.060
230
LYM115 Lymphoma, Non-Hodgkin 63 0.060
231
INT066 Interstitial Lung Disease 59 0.060
232
c LKM004 Leukemia, B-Cell, Chronic 24 0.060
233
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.060
234
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.060
235
c FNC027 Fanconi Anemia, Complementation Group a 71 0.060
236
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.060
237
P OST002 Osteoporosis 64 0.060
238
P MLT074 Multiple Endocrine Neoplasia 56 0.060
239
FRB001 Farber Lipogranulomatosis 53 0.060
240
P FNC004 Fanconi Syndrome 49 0.060
241
ATN005 Autonomic Dysfunction 49 0.060
242
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.060
243
P CHR562 Chronic Myelocytic Leukemia 41 0.060
244
P PNM006 Pneumoconiosis 51 0.059
245
P PRS040 Prostate Cancer 90 0.058
246
P OST012 Osteoarthritis 83 0.058
247
HV1006 Hiv-1 80 0.058
248
P FLL037 Follicular Lymphoma 70 0.058
249
P ART023 Arthropathy 64 0.058
250
P ESP024 Esophagitis 61 0.058
251
P NRV006 Nervous System Cancer 60 0.058
252
BNC003 Bone Cancer 58 0.058
253
LYM104 Lymphoma, Malt, Somatic 54 0.058
254
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.058
255
MRG003 Marginal Zone B-Cell Lymphoma 52 0.058
256
c FLL041 Follicular Lymphoma 1 45 0.058
257
SPL004 Splenic Marginal Zone Lymphoma 44 0.058
258
CLL014 Cll/sll 42 0.058
259
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.058
260
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.058
261
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 34 0.058
262
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 29 0.058
263
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.058
264
RFR001 Refractory Plasma Cell Neoplasm 16 0.058
265
c ACT071 Acute Kidney Failure 49 0.058
266
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.058
267
RNL025 Renal Hypoplasia 42 0.058
268
LYM127 Lymphatic Malformations 39 0.058
269
c DMN021 Diamond-Blackfan Anemia 6 35 0.058
270
c DMN017 Diamond-Blackfan Anemia 10 29 0.058
271
VSC001 Vascular Myelopathy 23 0.058
272
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.058
273
ANX002 Anxiety Disorder 67 0.058
274
LNG099 Lung Disease 64 0.058
275
FML039 Female Reproductive System Disease 48 0.058
276
PHY002 Physical Disorder 43 0.058
277
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.058
278
HDG012 Hodgkin Lymphoma 77 0.056
279
MNT001 Mantle Cell Lymphoma 72 0.056
280
c ADL017 Adult T-Cell Leukemia 60 0.056
281
P NRP001 Neuropathy 59 0.056
282
PRS047 Prostatitis 56 0.056
283
P CTN015 Cutaneous T Cell Lymphoma 50 0.056
284
END035 Endocrine Gland Cancer 49 0.056
285
ATN002 Autonomic Nervous System Disease 48 0.056
286
P TCL004 T-Cell Leukemia 47 0.056
287
MXD023 Mixed Cell Type Cancer 45 0.056
288
LKC003 Leukocyte Disease 43 0.056
289
VSC018 Visceral Steatosis 37 0.056
290
HDG004 Hodgkin's Granuloma 24 0.056
291
c LKM005 Leukemia, T-Cell, Chronic 20 0.056
292
HDG006 Hodgkin's Paragranuloma 17 0.056
293
c HYP595 Hypertension, Essential 69 0.056
294
RSP006 Respiratory System Disease 58 0.056
295
P MSC033 Muscle Disorders 52 0.056
296
P TRC086 Trichohepatoenteric Syndrome 1 48 0.056
297
P MDL005 Medulloblastoma 77 0.054
298
BRK010 Burkitt Lymphoma 69 0.054
299
MYC006 Mycosis Fungoides 66 0.054
300
P ALC004 Alcohol Abuse 59 0.054
301
DFF005 Diffuse Large B-Cell Lymphoma 59 0.054
302
ANR040 Aneurysm 57 0.054
303
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.054
304
SZR001 Sezary's Disease 52 0.054
305
RTC005 Reticulosarcoma 48 0.054
306
PTT009 Pituitary Gland Disease 47 0.054
307
RTC009 Reticulum Cell Sarcoma 47 0.054
308
PLS025 Plasmablastic Lymphoma 46 0.054
309
GND003 Gonadal Disease 39 0.054
310
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.054
311
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.054
312
PRM128 Primary Cutaneous Follicle Center Lymphoma 26 0.054
313
LYM048 Lymphoma, Large-Cell, Immunoblastic 25 0.054
314
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 0.054
315
BND002 B- and T-Cell Mixed Leukemia 17 0.054
316
HML018 Homologous Wasting Disease 13 0.054
317
OCL009 Ocular Cancer 59 0.054
318
LRN003 Learning Disability 49 0.054
319
c PLN021 Peeling Skin Syndrome 3 29 0.054
320
P MSC007 Muscle Hypertrophy 58 0.054
321
c HPT003 Hepatitis a 59 0.052
322
ART111 Artery Disease 55 0.052
323
P LTR001 Lateral Sclerosis 53 0.052
324
HPT074 Hepatic Adenoma, Somatic 50 0.052
325
HMC038 Hemochromatosis, Neonatal 29 0.052
326
HNM002 Hinman Syndrome 25 0.052
327
P HYP024 Hypoparathyroidism 53 0.052
328
P RNL015 Renal Hypertension 48 0.052
329
P OVR042 Ovarian Cancer 76 0.052
330
TST021 Testicular Germ Cell Tumor 69 0.052
331
EWN003 Ewing Sarcoma 66 0.052
332
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.052
333
WST001 West Syndrome 57 0.052
334
P OVR049 Ovarian Disease 56 0.052
335
GLM004 Gliomatosis Cerebri 49 0.052
336
CHL061 Childhood Leukemia 49 0.052
337
MSS002 Mass Syndrome 48 0.052
338
ANX004 Anoxia 43 0.052
339
HPT067 Hepatocellular Adenoma 42 0.052
340
BLR008 Bilirubin Metabolic Disorder 42 0.052
341
END038 Endocrine Pancreas Disease 41 0.052
342
GRM001 Germ Cell and Embryonal Cancer 36 0.052
343
17B002 17-Beta-Hydroxysteroid Dehydrogenase X Deficiency 31 0.052
344
c NRB015 Neuroblastoma 2 28 0.052
345
ARG006 Aregenerative Anemia 22 0.052
346
c CRN176 Coronary Heart Disease 9 18 0.052
347
c NRB013 Neuroblastoma 6 16 0.052
348
P CRN211 Coronary Artery Disease 74 0.051
349
CRB039 Cerebrovascular Disease 63 0.051
350
BRN071 Brain Injury 52 0.051
351
TCL003 T Cell Deficiency 45 0.051
352
GLC008 Glucose Metabolism Disease 42 0.051
353
AYM001 Ayme-Gripp Syndrome 41 0.051
354
c PLN018 Peeling Skin Syndrome 2 40 0.051
355
c PLN017 Peeling Skin Syndrome 1 34 0.051
356
ZYG002 Zygomycosis 33 0.051
357
c MLT136 Multiple Endocrine Neoplasia 1 69 0.049
358
ABL002 Ablepharon-Macrostomia Syndrome 57 0.049
359
CHR285 Chronic Myelomonocytic Leukemia 56 0.049
360
TST014 Testicular Cancer 53 0.049
361
c CHR417 Chronic Graft Versus Host Disease 51 0.049
362
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.049
363
DST006 Diastolic Heart Failure 46 0.049
364
PRP036 Peripheral T-Cell Lymphoma 45 0.049
365
TST015 Testicular Disease 44 0.049
366
OVR094 Ovarian Epithelial Cancer 43 0.049
367
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.049
368
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.049
369
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.049
370
EPS006 Epstein Syndrome 39 0.049
371
TST004 Testicular Lymphoma 37 0.049
372
OVR021 Ovarian Lymphoma 32 0.049
373
BRS001 Breast Lymphoma 32 0.049
374
TST003 Testicular Leukemia 31 0.049
375
c DMN006 Diamond-Blackfan Anemia 3 29 0.049
376
c DYS170 Dyserythropoietic Anemia, Congenital, Type Ii 28 0.049
377
c PNC111 Pancreatic Cancer 2 28 0.049
378
OVR056 Ovarian Primitive Germ Cell Tumor 28 0.049
379
c PNC094 Pancreatic Cancer 1 27 0.049
380
c DMN020 Diamond-Blackfan Anemia 8 26 0.049
381
OVR069 Ovarian Germ Cell Tumor 24 0.049
382
c PRM200 Primary Fanconi Syndrome 24 0.049
383
DFF027 Diffuse Lymphatic Malformation 22 0.049
384
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 22 0.049
385
BNP001 Bone Peripheral Neuroepithelioma 17 0.049
386
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 15 0.049
387
ETN001 Eating Disorder 58 0.049
388
PLS011 Plasmacytoma 56 0.049
389
P PNC001 Pancytopenia 52 0.049
390
MCR004 Macroglobulinemia 50 0.049
391
NSD001 Nose Disease 48 0.049
392
DWR001 Dwarfism 47 0.049
393
PRD011 Proud Syndrome 42 0.049
394
SXD001 Sex Differentiation Disease 38 0.049
395
c HMC021 Hemochromatosis, Type 2a 29 0.049
396
ANP010 Anaplastic Plasmacytoma 19 0.049
397
c DLT001 Delta Chain Disease 13 0.049
398
SKN016 Skin Disease 66 0.046
399
P EPL164 Epilepsy 66 0.046
400
VRL011 Viral Infectious Disease 55 0.046
401
BRN004 Brain Edema 52 0.046
402
c HPT015 Hepatitis D 52 0.046
403
FML038 Female Reproductive Organ Cancer 50 0.046
404
FML037 Female Breast Cancer 50 0.046
405
LPD009 Lipid Storage Disease 49 0.046
406
THY030 Thyroid Gland Disease 48 0.046
407
NTR003 Natural Killer Cell Leukemia 47 0.046
408
BLD053 Blood Platelet Disease 46 0.046
409
GRN017 Granulocytopenia 44 0.046
410
P DYS021 Dysautonomia 44 0.046
411
MLR006 Male Reproductive Organ Cancer 43 0.046
412
SXL003 Sexual Disorder 42 0.046
413
ANT018 Anthracosis 42 0.046
414
BND014 Bone Development Disease 40 0.046
415
MYF002 Myofascial Pain Syndrome 39 0.046
416
MLR007 Male Reproductive System Disease 34 0.046
417
ACR002 Acrocapitofemoral Dysplasia 33 0.046
418
CTN011 Cutaneous Porphyria 30 0.046
419
LPD027 Lip Disease 28 0.046
420
P GNR027 Generalized Peeling Skin Syndrome 19 0.046
421
c DYS033 Dysautonomia Like Disorder 16 0.046
422
PLM033 Pulmonary Embolism 60 0.046
423
P MYC008 Myocarditis 54 0.046
424
URM002 Uremia 48 0.046
425
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.046
426
P HRT035 Heart Block, Congenital 38 0.046
427
c DMN022 Diamond-Blackfan Anemia 9 26 0.046
428
VBR003 Vibrio Vulnificus Infection 23 0.046
429
c TFR001 Tfr2-Related Hereditary Hemochromatosis 13 0.046
430
BRN028 Brain Cancer 70 0.044
431
ART016 Aortic Aneurysm 69 0.044
432
CNN005 Connective Tissue Disease 62 0.044
433
P ADL010 Adult Respiratory Distress Syndrome 61 0.044
434
ALC006 Alcoholic Hepatitis 59 0.044
435
P HST010 Histiocytosis 58 0.044
436
P WLD002 Waldenstrom Macroglobulinemia 58 0.044
437
HRY003 Hairy Cell Leukemia 57 0.044
438
P ANP001 Anaplastic Large Cell Lymphoma 57 0.044
439
STR026 Star Syndrome 57 0.044
440
JNT002 Joint Disorders 55 0.044
441
P MMB011 Membranous Nephropathy 54 0.044
442
PST046 Post-Transplant Lymphoproliferative Disease 54 0.044
443
P LPC002 Lip Cancer 53 0.044
444
TTH006 Tooth Disease 52 0.044
445
INT007 Intermediate Coronary Syndrome 50 0.044
446
CLN015 Colon Adenocarcinoma 50 0.044
447
MST017 Mast Cell Disease 50 0.044
448
MST002 Mast-Cell Leukemia 48 0.044
449
ATR002 Atransferrinemia 48 0.044
450
LYM051 Lymphomatoid Granulomatosis 47 0.044
451
P ABD003 Abdominal Aortic Aneurysm 45 0.044
452
LYM012 Lymphoplasmacytic Lymphoma 44 0.044
453
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.044
454
MST006 Mast Syndrome 43 0.044
455
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.044
456
MST004 Mast Cell Neoplasm 40 0.044
457
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.044
458
SPC003 Specific Developmental Disorder 38 0.044
459
LTH001 Lethal Midline Granuloma 37 0.044
460
PRM026 Primary Systemic Mycosis 37 0.044
461
SLT001 Solitary Osseous Plasmacytoma 36 0.044
462
c CNN010 Connective Tissue Benign Neoplasm 32 0.044
463
RNL021 Renal Tubular Transport Disease 32 0.044
464
RFR002 Refractory Hairy Cell Leukemia 29 0.044
465
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.044
466
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 26 0.044
467
c MCR162 Macroglobulinemia, Waldenstrom 2 17 0.044
468
c ANP011 Anaplastic Small Cell Lymphoma 14 0.044
469
PRM165 Primary Plasmacytoma of the Bone 12 0.044
470
P HYP117 Hypertriglyceridemia 61 0.043
471
GTR002 Goiter 52 0.043
472
P TYR004 Tyrosinemia 45 0.043
473
DHY014 Dehydrated Hereditary Stomatocytosis with or Without Pseudohyperkalemia and/or Perinatal Edema 22 0.043
474
ESP021 Esophageal Cancer 76 0.041
475
CHR066 Chronic Fatigue Syndrome 64 0.041
476
SBS003 Substance Abuse 54 0.041
477
THL016 Thalassemias, Alpha- 53 0.041
478
P ACT135 Acute Graft Versus Host Disease 53 0.041
479
P SML016 Small Intestine Cancer 52 0.041
480
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.041
481
MYC002 Mycobacterium Avium Complex Disease 52 0.041
482
OCL006 Ocular Hypertension 48 0.041
483
INT054 Intraocular Lymphoma 45 0.041
484
CHR008 Choroiditis 44 0.041
485
RNL097 Renal Artery Disease 43 0.041
486
P CNN004 Connective Tissue Cancer 40 0.041
487
PRP080 Peripheral Artery Disease 37 0.041
488
c DYS156 Dyserythropoietic Anemia, Congenital, Type Ia 35 0.041
489
INT271 Interstitial Lung and Liver Disease 33 0.041
490
GLB003 Globe Disease 32 0.041
491
HFS001 Hfe-Associated Hereditary Hemochromatosis 29 0.041
492
c NRB014 Neuroblastoma 3 28 0.041
493
c DMN019 Diamond-Blackfan Anemia 4 27 0.041
494
ACQ016 Acquired Pure Red Cell Aplasia 25 0.041
495
HPD002 Hepadnavirus Infection 22 0.041
496
XLN067 X-Linked Protoporphyria 21 0.041
497
c NRB012 Neuroblastoma 5 18 0.041
498
LPN002 Lip and Oral Cavity Cancer 15 0.041
499
MLG026 Male Genital Organ Vascular Disease 14 0.041
500
P ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 12 0.041
501
P SCH015 Schizophrenia 77 0.038
502
ISC006 Ischemic Heart Disease 68 0.038
503
P HYP098 Hypereosinophilic Syndrome 63 0.038
504
ALC007 Alcohol Dependence 63 0.038
505
MXD005 Mixed Connective Tissue Disease 62 0.038
506
c SYS004 Systemic Mastocytosis 60 0.038
507
P CMR001 Camurati-Engelmann Disease 58 0.038
508
P HYP069 Hyperparathyroidism 58 0.038
509
c SVR001 Severe Acute Respiratory Syndrome 57 0.038
510
P MST009 Mastocytosis 56 0.038
511
LTT002 Letterer-Siwe Disease 56 0.038
512
PRP019 Peripheral Nervous System Disease 55 0.038
513
TTH002 Tooth Agenesis 54 0.038
514
P BRN009 Burning Mouth Syndrome 54 0.038
515
OLV001 Olivopontocerebellar Atrophy 53 0.038
516
BLM002 Bulimia Nervosa 52 0.038
517
MSS001 Masa Syndrome 52 0.038
518
P GND004 Gonadal Dysgenesis 51 0.038
519
c MLT086 Multiple Endocrine Neoplasia, Type Iv 51 0.038
520
CRN030 Coronary Stenosis 51 0.038
521
HND003 Hand-Foot-Uterus Syndrome 50 0.038
522
MSC072 Muscle Cancer 49 0.038
523
CTN014 Cutaneous Mastocytosis 49 0.038
524
ATY042 Atypical Chronic Myeloid Leukemia 48 0.038
525
ADR038 Adermatoglyphia 46 0.038
526
CHR563 Chronic Eosinophilic Leukemia 46 0.038
527
PTT037 Pituitary Tumors 45 0.038
528
c MTR002 Mitral Valve Insufficiency 44 0.038
529
BNN003 Bone Inflammation Disease 44 0.038
530
c HMN022 Human T-Cell Leukemia Virus Type 2 44 0.038
531
DFF001 Diffuse Cutaneous Mastocytosis 43 0.038
532
CHR286 Chronic Neutrophilic Leukemia 43 0.038
533
HYD046 Hydatidiform Mole, Recurrent, 1 41 0.038
534
CYS036 Cystinosis, Nephropathic 41 0.038
535
GST010 Gestational Trophoblastic Neoplasm 41 0.038
536
SML008 Small Intestine Lymphoma 40 0.038
537
P TST026 Testicular Germ Cell Cancer 39 0.038
538
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.038
539
c PRM149 Primary Hypereosinophilic Syndrome 38 0.038
540
MLG088 Malignant Germ Cell Tumor 38 0.038
541
LNG013 Lung Lymphoma 38 0.038
542
NSY001 N Syndrome 36 0.038
543
TRP005 Trophoblastic Neoplasm 36 0.038
544
SBS006 Sebastian Syndrome 35 0.038
545
P MXD016 Mixed Gonadal Dysgenesis 34 0.038
546
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.038
547
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.038
548
MXD032 Mixed Germ Cell Tumor 34 0.038
549
P XLN007 X-Linked Disease 34 0.038
550
P CHR084 Chromosomal Disease 32 0.038
551
P OVR075 Ovarian Dysgenesis 1 32 0.038
552
CVT001 Cavitary Optic Disc Anomalies 31 0.038
553
c OVR076 Ovarian Dysgenesis 2 31 0.038
554
MXD025 Mixed Germ Cell Cancer 31 0.038
555
c EYL003 Eye Lymphoma 30 0.038
556
UND007 Undifferentiated Connective Tissue Disease 30 0.038
557
c DMN018 Diamond-Blackfan Anemia 5 29 0.038
558
c DMN028 Diamond-Blackfan Anemia 12 27 0.038
559
GST059 Gestational Trophoblastic Tumor 26 0.038
560
c TST017 Testicular Malignant Germ Cell Cancer 24 0.038
561
PRM133 Primary Pulmonary Lymphoma 23 0.038
562
c OVR102 Ovarian Dysgenesis 3 22 0.038
563
SCK020 Sickle Cell - Hemoglobin D Disease 22 0.038
564
OVR015 Ovarian Mixed Germ Cell Neoplasm 21 0.038
565
ADL082 Adult Pulmonary Langerhans Cell Histiocytosis 21 0.038
566
TST040 Testicular Trophoblastic Tumor 20 0.038
567
NRC007 Neuroectodermal Endocrine Syndrome 19 0.038
568
VSC009 Vascular Skin Disease 19 0.038
569
PNL011 Pineal Region Germinoma 17 0.038
570
ISL032 Isolated Bone Marrow Mastocytosis 16 0.038
571
DSS003 Disseminated Eosinophilic Collagen Disease 15 0.038
572
c SML023 Small Cell Lung Cancer, Adult 15 0.038
573
WSC001 Wisconsin Syndrome 14 0.038
574
c SCN042 Secondary Hypereosinophilic Syndrome 14 0.038
575
c HMN023 Human T-Cell Leukemia Virus Type 3 14 0.038
576
LYM117 Lymphocytic Hypereosinophilic Syndrome 14 0.038
577
MXD024 Mixed Epithelial Tumor of Ovary 13 0.038
578
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 12 0.038
579
MLG035 Malignant Ovarian Mixed Epithelial Neoplasm 12 0.038
580
HDG010 Hodgkin Lymphoma, During Pregnancy 12 0.038
581
NNH004 Non-Hodgkin Lymphoma, During Pregnancy 12 0.038
582
P LNG028 Long Qt Syndrome 64 0.038
583
ADP002 Adiponectin Deficiency 30 0.038
584
BLN006 Blind Loop Syndrome 28 0.038
585
THY028 Thyroid Cancer 69 0.035
586
P ENC004 Encephalitis 63 0.035
587
KND001 Kindler Syndrome 57 0.035
588
PTT006 Pituitary Adenoma 56 0.035
589
DBN001 Dubin-Johnson Syndrome 54 0.035
590
PLM010 Pulmonary Edema 54 0.035
591
P APL006 Aplasia Cutis Congenita 52 0.035
592
PRC013 Pericarditis 51 0.035
593
P MSC003 Muscular Atrophy 50 0.035
594
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.035
595
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.035
596
TMR010 Tumor Predisposition Syndrome 47 0.035
597
PTT008 Pituitary Carcinoma 45 0.035
598
P PLM040 Pulmonary Valve Disease 43 0.035
599
VGN023 Vaginitis 42 0.035
600
NRR001 Neuroretinitis 42 0.035
601
P PNC045 Pancreatic Agenesis 42 0.035
602
ACT103 Acute Lymphoblastic Leukemia, Childhood 41 0.035
603
HRT012 Heart Valve Disease 40 0.035
604
PDT001 Pediatric Lymphoma 38 0.035
605
NNF001 Non-Functioning Pancreatic Endocrine Tumor 35 0.035
606
c MYL058 Myeloproliferative Syndrome, Transient 33 0.035
607
MTL005 Metal Allergy 33 0.035
608
KDN013 Kidney Hypertrophy 31 0.035
609
FNC012 Functioning Pancreatic Endocrine Tumor 31 0.035
610
GST014 Gastrointestinal Lymphoma 31 0.035
611
PTT001 Pituitary Hypoplasia 31 0.035
612
JNS003 Jensen Syndrome 31 0.035
613
PNC092 Pancreatic Agenesis and Congenital Heart Defects 30 0.035
614
HRZ001 Huriez Syndrome 30 0.035
615
HRT003 Heart Lymphoma 30 0.035
616
MNG003 Mungan Syndrome 22 0.035
617
c PNC105 Pancreatic Agenesis 2 21 0.035
618
CRT057 Critical Congenital Heart Disease 20 0.035
619
PNC007 Pancreas Lymphoma 17 0.035
620
MYC003 Myocardium Cancer 14 0.035
621
CMP052 Complication in Hemodialysis 13 0.035
622
P MSC005 Muscular Dystrophy 65 0.030
623
c ATM011 Autoimmune Hepatitis 60 0.030
624
SPT004 Septic Arthritis 60 0.030
625
P GLM007 Glomerulonephritis 59 0.030
626
P GT001 Gout 58 0.030
627
P MTR012 Mitral Valve Disease 58 0.030
628
CRT002 Cartilage-Hair Hypoplasia 57 0.030
629
BRN002 Bronchiolitis 56 0.030
630
HPT022 Hepatoblastoma 55 0.030
631
LST001 Listeriosis 53 0.030
632
PRC012 Pericardial Effusion 51 0.030
633
HPT046 Hepatic Veno-Occlusive Disease 50 0.030
634
PRP032 Porphyria Variegata 50 0.030
635
HPT009 Hepatopulmonary Syndrome 48 0.030
636
RNL077 Renal Fibrosis 47 0.030
637
ADN001 Adenosine Deaminase Deficiency 45 0.030
638
RNL011 Renal Osteodystrophy 45 0.030
639
CRD001 Cardiac Tamponade 44 0.030
640
HRT008 Heart Conduction Disease 42 0.030
641
GRW015 Growth Hormone Deficiency, Isolated, Type Ia 41 0.030
642
P MCR240 Microcephalic Osteodysplastic Primordial Dwarfism, Type I 38 0.030
643
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.030
644
PRR013 Prurigo Nodularis 35 0.030
645
RHS001 Rh Isoimmunization 28 0.030
646
WRF003 Warfarin Syndrome 28 0.030
647
SPN331 Spondyloocular Syndrome 27 0.030
648
P STM009 Stomatocytosis I 26 0.030