Search results for iron overload

397 hits were found for iron overload

# Family MCID Name MIFTS Score
1
IRN008 Iron Overload in Africa 32 8.334
2
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 16 7.394
3
c HMC034 Hemochromatosis, Type 5 30 7.330
4
GRC001 Gracile Syndrome 31 5.812
5
c ANM027 Anemia, Hypochromic Microcytic, with Iron Overload 2 24 5.789
6
HMS001 Hemosiderosis 50 5.574
7
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 24 5.254
8
c HMC009 Hemochromatosis Type 2 43 2.710
9
GNT037 Genetic Hyperferritinemia Without Iron Overload 10 2.628
10
FRR002 Ferro-Cerebro-Cutaneous Syndrome 10 2.590
11
P ZLL001 Zellweger Syndrome 56 2.560
12
IRN002 Iron Metabolism Disease 45 0.737
13
IRN001 Iron Deficiency Anemia 55 0.611
14
DFC004 Deficiency Anemia 62 0.550
15
P THL005 Thalassemia 65 0.501
16
P HPT021 Hepatitis 75 0.404
17
c HMC039 Hemochromatosis, Type 1 71 0.351
18
c BTT014 Beta-Thalassemia 70 0.335
19
HMG005 Hemoglobinopathy 53 0.273
20
P KDN018 Kidney Disease 69 0.262
21
MYL009 Myelodysplastic Syndrome 75 0.255
22
c CHR089 Chronic Kidney Failure 72 0.230
23
c HPT001 Hepatitis C 73 0.223
24
SCK005 Sickle Cell Disease 54 0.222
25
AGN016 Aging 65 0.220
26
SCK003 Sickle Cell Anemia 73 0.219
27
P LVR013 Liver Disease 76 0.214
28
CNG034 Congestive Heart Failure 74 0.212
29
P SDR002 Siderosis 48 0.210
30
URN009 Urinary System Disease 58 0.206
31
P LKM002 Leukemia 75 0.201
32
P PRP029 Porphyria 62 0.193
33
c HMC010 Hemochromatosis, Type 3 42 0.190
34
c BLD140 Blood Group, I System 37 0.187
35
NRN002 Neuronitis 43 0.186
36
P PRP003 Porphyria Cutanea Tarda 67 0.186
37
MCR018 Microcytic Anemia 43 0.183
38
HYP266 Hypoxia 61 0.174
39
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.171
40
P HRT032 Heart Disease 80 0.167
41
P SDR003 Sideroblastic Anemia 43 0.158
42
APL001 Aplastic Anemia 74 0.154
43
ACR006 Aceruloplasminemia 65 0.151
44
HMT018 Hematopoietic Stem Cell Transplantation 58 0.150
45
END072 Endotheliitis 46 0.147
46
LVR012 Liver Cirrhosis 73 0.145
47
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.142
48
c ANM036 Anemia, Sideroblastic, 1 55 0.142
49
P HPT023 Hepatocellular Carcinoma 94 0.140
50
P LYM118 Lymphoma 71 0.140
51
NNL002 Nonalcoholic Steatohepatitis 56 0.139
52
c HPT073 Hepatitis C Virus 73 0.136
53
END030 End Stage Renal Failure 59 0.134
54
DDN006 Duodenitis 46 0.129
55
RTN023 Retinitis 52 0.126
56
P PLM037 Pulmonary Hypertension 79 0.126
57
LNG099 Lung Disease 67 0.124
58
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.123
59
P MYL006 Myeloid Leukemia 69 0.123
60
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.122
61
P LYM026 Lymphoblastic Leukemia 66 0.121
62
FTT001 Fatty Liver Disease 62 0.120
63
c HMC035 Hemochromatosis, Type 4 40 0.120
64
c LKM061 Leukemia, Acute Myeloid 81 0.119
65
P DMN001 Diamond-Blackfan Anemia 70 0.119
66
LYM019 Lymphosarcoma 58 0.118
67
P ART022 Arthritis 77 0.118
68
PYR041 Pyruvate Kinase Deficiency of Red Cells 54 0.117
69
c ACT073 Acute Leukemia 61 0.117
70
CNG028 Congenital Hypoplastic Anemia 50 0.115
71
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.114
72
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.114
73
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.114
74
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.114
75
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.114
76
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.114
77
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.114
78
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.114
79
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.114
80
PRR002 Pure Red-Cell Aplasia 52 0.113
81
LYM024 Lymphatic System Disease 45 0.110
82
P MYC084 Mycobacterium Tuberculosis 1 69 0.110
83
P CNG003 Congenital Dyserythropoietic Anemia 42 0.107
84
ISC004 Ischemia 66 0.107
85
LYM067 Lymphoid Leukemia 43 0.107
86
P HYP086 Hypothyroidism 62 0.106
87
ATR002 Atransferrinemia 52 0.106
88
HYP001 Hypochromic Microcytic Anemia 34 0.106
89
HYP080 Hypogonadism 54 0.104
90
ANX010 Anxiety 72 0.102
91
P DBT009 Diabetes Mellitus 72 0.102
92
HYP801 Hyperferritinemia with or Without Cataract 39 0.102
93
RFR010 Refractory Anemia 48 0.102
94
P FRD012 Friedreich Ataxia 1 58 0.102
95
CRB009 Cerebritis 41 0.102
96
HMC038 Hemochromatosis, Neonatal 38 0.101
97
c LKM062 Leukemia, Acute Lymphoblastic 64 0.101
98
P ACT074 Acute Lymphocytic Leukemia 61 0.101
99
P MYL005 Myelofibrosis 75 0.100
100
P BRS047 Breast Cancer 100 0.099
101
SPS003 Spastic Diplegia 55 0.099
102
ACT118 Acute Non Lymphoblastic Leukemia 32 0.098
103
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 32 0.098
104
P CTR002 Cataract 60 0.097
105
MYL069 Myeloma, Multiple 86 0.096
106
ALR002 Al-Raqad Syndrome 30 0.096
107
P HML002 Hemolytic Anemia 62 0.096
108
HYP060 Hyperinsulinism 56 0.096
109
ANX004 Anoxia 49 0.094
110
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.094
111
RSP006 Respiratory System Disease 63 0.093
112
PLC008 Placenta Disease 48 0.093
113
c HMC021 Hemochromatosis, Type 2a 36 0.092
114
P ANR048 Aniridia 1 68 0.092
115
ANR038 Anorexia Nervosa 1 21 0.092
116
BLD137 Blood Group--Ahonen 17 0.092
117
MNT002 Mental Depression 60 0.091
118
P NRB001 Neuroblastoma 73 0.090
119
THR024 Thrombosis 61 0.090
120
P ADN016 Adenocarcinoma 71 0.088
121
WLS001 Wilson Disease 72 0.088
122
P RTN016 Retinal Degeneration 56 0.088
123
P BLD051 Blood Coagulation Disease 38 0.088
124
MYL031 Myeloproliferative Neoplasm 64 0.088
125
P PLM085 Pulmonary Hemosiderosis 48 0.087
126
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.087
127
P INF032 Infertility 59 0.087
128
P HMR003 Hemorrhagic Disease 61 0.086
129
VSC008 Vascular Hemostatic Disease 36 0.086
130
P MYC007 Myocardial Infarction 81 0.085
131
MLN008 Melanoma 72 0.085
132
PRT118 Protoporphyria, Erythropoietic 58 0.085
133
P PNC044 Pancreatitis 64 0.085
134
P ENC018 Encephalopathy 58 0.085
135
HPT082 Hepatic Adenomas, Familial 52 0.085
136
P HRD011 Hereditary Spherocytosis 55 0.084
137
PLS009 Plasma Cell Neoplasm 51 0.084
138
SYS003 Systolic Heart Failure 44 0.084
139
c TRC078 Trichohepatoenteric Syndrome 2 34 0.084
140
P MLT020 Multiple Sclerosis 85 0.082
141
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.082
142
VRL011 Viral Infectious Disease 64 0.082
143
P HMG032 Hemoglobin H Disease 53 0.082
144
c HPT016 Hepatitis B 68 0.081
145
ADN018 Adenoma 63 0.081
146
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 25 0.081
147
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 32 0.080
148
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.079
149
P LCT001 Lactic Acidosis 51 0.079
150
c ALP101 Alpha-Thalassemia 60 0.079
151
ATN005 Autonomic Dysfunction 51 0.079
152
GLC008 Glucose Metabolism Disease 38 0.079
153
CHL068 Cholestasis 60 0.077
154
AMN006 Aminoaciduria 41 0.077
155
P SCK034 Sickle Beta Thalassemia 29 0.077
156
P GRF003 Graft-Versus-Host Disease 72 0.077
157
ANR040 Aneurysm 61 0.077
158
BRN106 Burns 57 0.077
159
c LKM071 Leukemia, Chronic Lymphocytic 75 0.077
160
P ART023 Arthropathy 68 0.077
161
P NRP001 Neuropathy 63 0.077
162
c VRL010 Viral Hepatitis 59 0.077
163
c LKM004 Leukemia, B-Cell, Chronic 37 0.077
164
OST012 Osteoarthritis 88 0.074
165
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.074
166
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 33 0.074
167
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 26 0.074
168
P OST002 Osteoporosis 75 0.074
169
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.074
170
P PNM006 Pneumoconiosis 55 0.073
171
P TRC086 Trichohepatoenteric Syndrome 1 54 0.073
172
P PRS040 Prostate Cancer 88 0.072
173
P FLL037 Follicular Lymphoma 76 0.072
174
ALP046 Alport Syndrome, X-Linked 74 0.072
175
P BCL006 B-Cell Lymphomas 70 0.072
176
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.072
177
P ESP024 Esophagitis 64 0.072
178
PRS047 Prostatitis 59 0.072
179
MRG003 Marginal Zone B-Cell Lymphoma 56 0.072
180
SPL004 Splenic Marginal Zone Lymphoma 52 0.072
181
NDL020 Nodal Marginal Zone B-Cell Lymphoma 38 0.072
182
P VSC018 Visceral Steatosis 38 0.072
183
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 36 0.072
184
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.071
185
LYM133 Lymphoma, Hodgkin, Classic 78 0.069
186
MNT001 Mantle Cell Lymphoma 76 0.069
187
P CTN015 Cutaneous T Cell Lymphoma 56 0.069
188
HDG004 Hodgkin's Granuloma 28 0.069
189
HDG006 Hodgkin's Paragranuloma 21 0.069
190
P CRN300 Coronary Heart Disease 1 57 0.069
191
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.068
192
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.068
193
P LTR001 Lateral Sclerosis 58 0.067
194
IMM136 Immune System Disease 57 0.067
195
ANT018 Anthracosis 39 0.067
196
MYC006 Mycosis Fungoides 73 0.067
197
BRK010 Burkitt Lymphoma 71 0.067
198
DFF005 Diffuse Large B-Cell Lymphoma 64 0.067
199
c ADL017 Adult T-Cell Leukemia 63 0.067
200
PLM033 Pulmonary Embolism 62 0.067
201
SZR001 Sezary's Disease 58 0.067
202
LYM040 Lymphoblastic Lymphoma 58 0.067
203
PLS025 Plasmablastic Lymphoma 51 0.067
204
RTC009 Reticulum Cell Sarcoma 51 0.067
205
P TCL004 T-Cell Leukemia 50 0.067
206
RTC005 Reticulosarcoma 49 0.067
207
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.067
208
INT038 Interdigitating Dendritic Cell Sarcoma 46 0.067
209
HPT067 Hepatocellular Adenoma 43 0.067
210
LYM048 Lymphoma, Large-Cell, Immunoblastic 31 0.067
211
HML018 Homologous Wasting Disease 18 0.067
212
c ART101 Aortic Valve Disease 2 65 0.066
213
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.065
214
P CRN018 Coronary Artery Anomaly 69 0.065
215
c HPT003 Hepatitis a 63 0.065
216
ATN002 Autonomic Nervous System Disease 51 0.065
217
P DYS021 Dysautonomia 47 0.065
218
P CNN004 Connective Tissue Cancer 35 0.065
219
P HYP024 Hypoparathyroidism 55 0.064
220
P OVR042 Ovarian Cancer 82 0.064
221
P FNC027 Fanconi Anemia, Complementation Group a 78 0.064
222
P ALC004 Alcohol Abuse 63 0.064
223
c OVR114 Ovarian Cancer 1 54 0.064
224
P FNC004 Fanconi Syndrome 54 0.064
225
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.064
226
EWN002 Ewing's Family of Tumors 49 0.064
227
c CNG027 Congenital Hemolytic Anemia 46 0.064
228
ARG006 Aregenerative Anemia 26 0.064
229
BRS051 Breast Disease 67 0.062
230
MCR004 Macroglobulinemia 54 0.062
231
ART140 Arteries, Anomalies of 51 0.062
232
PNC001 Pancytopenia 50 0.062
233
ZYG002 Zygomycosis 35 0.062
234
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.060
235
P CHR285 Chronic Myelomonocytic Leukemia 63 0.060
236
URM002 Uremia 52 0.060
237
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 40 0.060
238
VBR003 Vibrio Vulnificus Infection 24 0.060
239
JNT002 Joint Disorders 60 0.060
240
PLS011 Plasmacytoma 60 0.060
241
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.060
242
CTN011 Cutaneous Porphyria 30 0.060
243
RFR001 Refractory Plasma Cell Neoplasm 19 0.060
244
P EPL164 Epilepsy 70 0.057
245
CRB039 Cerebrovascular Disease 68 0.057
246
c PRC016 Pre-Eclampsia 65 0.057
247
BRN004 Brain Edema 57 0.057
248
THY030 Thyroid Gland Disease 51 0.057
249
GRN017 Granulocytopenia 49 0.057
250
MYF002 Myofascial Pain Syndrome 44 0.057
251
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 43 0.057
252
HFS001 Hfe-Associated Hereditary Hemochromatosis 21 0.057
253
ALP103 Alpha-1-Antitrypsin Deficiency 60 0.057
254
P MYC008 Myocarditis 58 0.057
255
GTR002 Goiter 53 0.057
256
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 0.057
257
TFR001 Tfr2-Related Hereditary Hemochromatosis 6 0.057
258
ESP021 Esophageal Cancer 79 0.054
259
c MCL042 Macular Degeneration, Age-Related, 1 79 0.054
260
ISC006 Ischemic Heart Disease 73 0.054
261
ART016 Aortic Aneurysm 70 0.054
262
P ADL010 Adult Respiratory Distress Syndrome 67 0.054
263
P WLD002 Waldenstrom Macroglobulinemia 65 0.054
264
P ANP001 Anaplastic Large Cell Lymphoma 60 0.054
265
P HST010 Histiocytosis 60 0.054
266
HRY003 Hairy Cell Leukemia 60 0.054
267
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.054
268
PTT009 Pituitary Gland Disease 56 0.054
269
LYM051 Lymphomatoid Granulomatosis 51 0.054
270
MST002 Mast-Cell Leukemia 51 0.054
271
LYM012 Lymphoplasmacytic Lymphoma 50 0.054
272
CHR008 Choroiditis 47 0.054
273
ANG046 Angioimmunoblastic T-Cell Lymphoma 46 0.054
274
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 44 0.054
275
LTH001 Lethal Midline Granuloma 40 0.054
276
SPN331 Spondyloocular Syndrome 34 0.054
277
RFR002 Refractory Hairy Cell Leukemia 32 0.054
278
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 29 0.054
279
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 28 0.054
280
RNL021 Renal Tubular Transport Disease 27 0.054
281
PRT094 Protoporphyria, Erythropoietic, X-Linked 27 0.054
282
c LKM005 Leukemia, T-Cell, Chronic 25 0.054
283
XLN067 X-Linked Protoporphyria 18 0.054
284
CLS052 Classic Hairy Cell Leukemia 16 0.054
285
P HYP014 Hyperuricemia 54 0.054
286
P HYP750 Hypertriglyceridemia, Familial 55 0.052
287
P TYR004 Tyrosinemia 48 0.052
288
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.052
289
c DMN020 Diamond-Blackfan Anemia 8 20 0.052
290
c LKM063 Leukemia, Chronic Myeloid 80 0.051
291
P OVR049 Ovarian Disease 58 0.051
292
c ACT071 Acute Kidney Failure 54 0.051
293
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 37 0.051
294
GND003 Gonadal Disease 32 0.051
295
c PRP091 Porphyria Cutanea Tarda, Type I 31 0.051
296
c ANM034 Anemia, Sideroblastic, 4 17 0.051
297
HPD002 Hepadnavirus Infection 14 0.051
298
PST092 Posttransplant Acute Limbic Encephalitis 11 0.051
299
P SCH015 Schizophrenia 71 0.047
300
P TST021 Testicular Germ Cell Tumor 70 0.047
301
P HYP098 Hypereosinophilic Syndrome 65 0.047
302
c CHR417 Chronic Graft Versus Host Disease 65 0.047
303
ALC007 Alcohol Dependence 65 0.047
304
MST017 Mast Cell Disease 63 0.047
305
LNG108 Langerhans Cell Histiocytosis 63 0.047
306
ALC006 Alcoholic Hepatitis 62 0.047
307
P CMR001 Camurati-Engelmann Disease 62 0.047
308
OCL009 Ocular Cancer 61 0.047
309
P HYP069 Hyperparathyroidism 58 0.047
310
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.047
311
TST014 Testicular Cancer 54 0.047
312
CRD223 Cardiac Arrhythmia 52 0.047
313
CHR563 Chronic Eosinophilic Leukemia 51 0.047
314
ATY042 Atypical Chronic Myeloid Leukemia 51 0.047
315
INT054 Intraocular Lymphoma 50 0.047
316
CHL061 Childhood Leukemia 50 0.047
317
ESN011 Eisenmenger Syndrome 49 0.047
318
CHR286 Chronic Neutrophilic Leukemia 49 0.047
319
PRP036 Peripheral T-Cell Lymphoma 48 0.047
320
c DMN023 Diamond-Blackfan Anemia 1 48 0.047
321
OVR094 Ovarian Epithelial Cancer 46 0.047
322
c MTR002 Mitral Valve Insufficiency 46 0.047
323
SML008 Small Intestine Lymphoma 45 0.047
324
P TST026 Testicular Germ Cell Cancer 44 0.047
325
HPT070 Hepatosplenic T-Cell Lymphoma 43 0.047
326
TST015 Testicular Disease 43 0.047
327
OVR112 Ovarian Germ Cell Cancer 42 0.047
328
TST004 Testicular Lymphoma 42 0.047
329
LTT002 Letterer-Siwe Disease 39 0.047
330
GST010 Gestational Trophoblastic Neoplasm 38 0.047
331
TRP005 Trophoblastic Neoplasm 37 0.047
332
P GRM010 Germ Cells Tumors 37 0.047
333
LKC003 Leukocyte Disease 34 0.047
334
GST059 Gestational Trophoblastic Tumor 30 0.047
335
MTL002 Metal Metabolism Disorder 30 0.047
336
MST020 Mast Cell Activation Syndrome 30 0.047
337
c PRM200 Primary Fanconi Syndrome 27 0.047
338
ACQ031 Acquired Idiopathic Sideroblastic Anemia 24 0.047
339
P HMG026 Hemoglobin E-Beta-Thalassemia Syndrome 20 0.047
340
PNL011 Pineal Region Germinoma 20 0.047
341
DSS003 Disseminated Eosinophilic Collagen Disease 20 0.047
342
P DLT002 Dilated Cardiomyopathy 76 0.047
343
P LNG028 Long Qt Syndrome 63 0.047
344
CHR066 Chronic Fatigue Syndrome 67 0.043
345
P ENC004 Encephalitis 66 0.043
346
VGN023 Vaginitis 59 0.043
347
PLM010 Pulmonary Edema 57 0.043
348
DBN001 Dubin-Johnson Syndrome 56 0.043
349
P MSC003 Muscular Atrophy 55 0.043
350
PRC013 Pericarditis 55 0.043
351
P DBT005 Diabetes Insipidus 54 0.043
352
c HPT015 Hepatitis D 52 0.043
353
c INH020 Inherited Metabolic Disorder 49 0.043
354
NRR001 Neuroretinitis 46 0.043
355
HRT012 Heart Valve Disease 45 0.043
356
OST062 Osteoarthritis with Mild Chondrodysplasia 43 0.043
357
MNR003 Mineral Metabolism Disease 33 0.043
358
P ANM033 Anemia, Sideroblastic, 2, Pyridoxine-Refractory 22 0.043
359
HRT038 Heart, Malformation of 22 0.043
360
P STM009 Stomatocytosis I 16 0.043
361
c ATM011 Autoimmune Hepatitis 63 0.037
362
P NRN021 Neuronal Ceroid Lipofuscinosis 62 0.037
363
P GLM007 Glomerulonephritis 61 0.037
364
SPT004 Septic Arthritis 60 0.037
365
GT001 Gout 60 0.037
366
BRN002 Bronchiolitis 59 0.037
367
LPD008 Lipid Metabolism Disorder 59 0.037
368
CRT002 Cartilage-Hair Hypoplasia 58 0.037
369
HPT046 Hepatic Veno-Occlusive Disease 56 0.037
370
HPT022 Hepatoblastoma 55 0.037
371
P MMB011 Membranous Nephropathy 55 0.037
372
LST001 Listeriosis 55 0.037
373
PRP032 Porphyria Variegata 54 0.037
374
HPT009 Hepatopulmonary Syndrome 53 0.037
375
CLN015 Colon Adenocarcinoma 53 0.037
376
ADN001 Adenosine Deaminase Deficiency 52 0.037
377
CRN030 Coronary Stenosis 52 0.037
378
P PRC012 Pericardial Effusion 52 0.037
379
HYD012 Hydrops Fetalis 50 0.037
380
RNL011 Renal Osteodystrophy 49 0.037
381
RNL077 Renal Fibrosis 49 0.037
382
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.037
383
CRD001 Cardiac Tamponade 45 0.037
384
CHP002 Chops Syndrome 40 0.037
385
PRR013 Prurigo Nodularis 39 0.037
386
OVR093 Overhydrated Hereditary Stomatocytosis 35 0.037
387
c HMG003 Hemoglobin E Disease 34 0.037
388
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.037
389
HMP001 Hemopericardium 34 0.037
390
c INF145 Infantile Liver Failure Syndrome 1 33 0.037
391
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.037
392
WRF003 Warfarin Syndrome 31 0.037
393
RHS001 Rh Isoimmunization 30 0.037
394
c DMN021 Diamond-Blackfan Anemia 6 25 0.037
395
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.037
396
c DMN019 Diamond-Blackfan Anemia 4 23 0.037
397
c DMN024 Diamond-Blackfan Anemia 7 23 0.037
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