Search results for "alloimmunization"

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

616 hits were found for 'alloimmunization'

# Family MCID Name MIFTS Score
1
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 26 4.031
2
c CNG407 Congenital Membranous Nephropathy Due to Maternal Anti-Neutral Endopeptidase Alloimmunization 9 3.918
3
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 29 3.222
4
THR095 Thrombocytopenia, Neonatal Alloimmune 8 3.222
5
HML043 Hemolytic Disease of the Newborn with Kell Alloimmunization 5 3.209
6
NTR014 Neutropenia, Alloimmune Neonatal 5 2.287
7
THR100 Thrombocytopenic Purpura, Autoimmune 47 2.269
8
P THR014 Thrombocytopenia 50 0.193
9
P NTR004 Neutropenia 50 0.113
10
P SCK005 Sickle Cell Disease 49 0.093
11
P THL005 Thalassemia 56 0.080
12
NNT016 Neonatal Hemochromatosis 37 0.075
13
P HMC003 Hemochromatosis 75 0.069
14
P LVR013 Liver Disease 59 0.069
15
PRP030 Purpura 47 0.069
16
SCK003 Sickle Cell Anemia 71 0.063
17
P HML002 Hemolytic Anemia 52 0.063
18
HYD012 Hydrops Fetalis 50 0.063
19
P MMB011 Membranous Nephropathy 43 0.056
20
END072 Endotheliitis 39 0.056
21
P APL001 Aplastic Anemia 70 0.049
22
P PRM002 Primary Hyperoxaluria 64 0.049
23
P LKM002 Leukemia 61 0.049
24
P KDN018 Kidney Disease 57 0.049
25
c ATM010 Autoimmune Hemolytic Anemia 56 0.049
26
THR013 Thoracic Outlet Syndrome 47 0.049
27
HMT018 Hematopoietic Stem Cell Transplantation 45 0.049
28
P TRC086 Trichohepatoenteric Syndrome 1 42 0.049
29
MMB002 Membranous Glomerulonephritis 40 0.049
30
THR035 Thrombasthenia 36 0.049
31
BLD053 Blood Platelet Disease 32 0.049
32
P ATX030 Ataxia-Telangiectasia 76 0.040
33
c LKM061 Leukemia, Acute Myeloid 74 0.040
34
P NRB001 Neuroblastoma 73 0.040
35
MYL009 Myelodysplastic Syndrome 69 0.040
36
c SPN225 Spondyloarthropathy 1 66 0.040
37
P ANG001 Angelman Syndrome 66 0.040
38
AND015 Androgen Insensitivity 65 0.040
39
GLN010 Glanzmann Thrombasthenia 65 0.040
40
c HMP029 Hemophilia a 64 0.040
41
P HRM001 Hermansky-Pudlak Syndrome 62 0.040
42
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.040
43
c PNC108 Pancreatitis, Hereditary 59 0.040
44
LVR012 Liver Cirrhosis 59 0.040
45
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.040
46
P MYL006 Myeloid Leukemia 59 0.040
47
ART001 Arterial Tortuosity Syndrome 59 0.040
48
P HPT021 Hepatitis 58 0.040
49
P AND016 Andersen Syndrome 58 0.040
50
VND002 Van Der Woude Syndrome 54 0.040
51
DFC004 Deficiency Anemia 52 0.040
52
P NPH012 Nephrotic Syndrome 52 0.040
53
HNT002 Hantavirus Pulmonary Syndrome 52 0.040
54
c MTB001 Metabolic Syndrome X 52 0.040
55
P HMP007 Hemophilia 51 0.040
56
P VNT002 Ventricular Septal Defect 50 0.040
57
P CNJ013 Conjunctivitis 50 0.040
58
P SHR029 Short Syndrome 49 0.040
59
c ACT073 Acute Leukemia 49 0.040
60
P GLM007 Glomerulonephritis 49 0.040
61
THR004 Thrombocytosis 48 0.040
62
BNM001 Bone Marrow Cancer 47 0.040
63
c ART101 Aortic Valve Disease 2 46 0.040
64
MYC002 Mycobacterium Avium Complex Disease 46 0.040
65
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.040
66
FCT013 Factor V Leiden Thrombophilia 43 0.040
67
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.040
68
P PRN026 Porencephaly 42 0.040
69
P PNC001 Pancytopenia 41 0.040
70
c CHR417 Chronic Graft Versus Host Disease 41 0.040
71
P SDR002 Siderosis 40 0.040
72
P HYP071 Hypersensitivity Reaction Type Ii Disease 38 0.040
73
PRP036 Peripheral T-Cell Lymphoma 37 0.040
74
IRN002 Iron Metabolism Disease 36 0.040
75
HRT011 Heart Septal Defect 35 0.040
76
ADS002 Adie Syndrome 34 0.040
77
P GLM044 Glomerular Disease 32 0.040
78
HPT074 Hepatic Adenoma, Somatic 30 0.040
79
FTL004 Fetal Erythroblastosis 30 0.040
80
IDP077 Idiopathic Membranous Glomerulonephritis 29 0.040
81
TFT003 Tufting Enteropathy 27 0.040
82
HNM002 Hinman Syndrome 27 0.040
83
BLD052 Blood Group Incompatibility 26 0.040
84
ATM012 Autoimmune Disease of Blood 24 0.040
85
ALR002 Al-Raqad Syndrome 23 0.040
86
c BNG076 Benign Exophthalmos Syndrome 21 0.040
87
P BRS047 Breast Cancer 100 0.028
88
P ALZ034 Alzheimer Disease 98 0.028
89
P CLR023 Colorectal Cancer 95 0.028
90
P LNG032 Lung Cancer 91 0.028
91
HPT023 Hepatocellular Carcinoma 90 0.028
92
P PRS040 Prostate Cancer 90 0.028
93
CYS001 Cystic Fibrosis 90 0.028
94
c SYS001 Systemic Lupus Erythematosus 90 0.028
95
P OBS005 Obesity 89 0.028
96
P RHM011 Rheumatoid Arthritis 88 0.028
97
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.028
98
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.028
99
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.028
100
P RNL014 Renal Cell Carcinoma 81 0.028
101
CRH001 Crohn's Disease 80 0.028
102
P RTT002 Rett Syndrome 79 0.028
103
P HYP607 Hypercholesterolemia, Familial 79 0.028
104
P SCH015 Schizophrenia 79 0.028
105
P OST012 Osteoarthritis 79 0.028
106
P LFR001 Li-Fraumeni Syndrome 79 0.028
107
P PNC035 Pancreatic Cancer 78 0.028
108
P HNT016 Huntington Disease 78 0.028
109
DCH001 Duchenne Muscular Dystrophy 78 0.028
110
P AST005 Asthma 77 0.028
111
HV1006 Hiv-1 77 0.028
112
c MLT019 Multiple Myeloma 77 0.028
113
P MYC007 Myocardial Infarction 76 0.028
114
GLC006 Galactosemia 76 0.028
115
P PHC003 Pheochromocytoma 76 0.028
116
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 0.028
117
HDG012 Hodgkin Lymphoma 75 0.028
118
FBR012 Fabry Disease 75 0.028
119
c MCL042 Macular Degeneration, Age-Related, 1 74 0.028
120
c PRK057 Parkinson Disease, Late-Onset 73 0.028
121
MRF001 Marfan Syndrome 72 0.028
122
MLR004 Malaria 72 0.028
123
ANR002 Aniridia 72 0.028
124
SQM013 Squamous Cell Carcinoma, Head and Neck 71 0.028
125
ADN021 Adenomatous Polyposis Coli 71 0.028
126
CDS001 Cadasil 70 0.028
127
c CHR090 Chronic Lymphocytic Leukemia 70 0.028
128
P OST005 Osteogenesis Imperfecta 70 0.028
129
ESP021 Esophageal Cancer 69 0.028
130
P MDL005 Medulloblastoma 69 0.028
131
c MCP003 Mucopolysaccharidosis Vii 69 0.028
132
P OVR042 Ovarian Cancer 69 0.028
133
P SCL016 Scleroderma 69 0.028
134
c HYP595 Hypertension, Essential 68 0.028
135
P WSK001 Wiskott-Aldrich Syndrome 68 0.028
136
P CRN211 Coronary Artery Disease 68 0.028
137
P CNG401 Congenital Heart Disease 68 0.028
138
STR067 Stroke, Ischemic 68 0.028
139
TTR001 Tetralogy of Fallot 68 0.028
140
P BRD002 Bardet-Biedl Syndrome 68 0.028
141
BRK010 Burkitt Lymphoma 68 0.028
142
END057 Endometrial Cancer 67 0.028
143
GLL008 Gilles De La Tourette Syndrome 67 0.028
144
P CYS013 Cystinuria 67 0.028
145
BCK001 Becker Muscular Dystrophy 66 0.028
146
P FRG001 Fragile X Syndrome 66 0.028
147
P RBN001 Rubinstein-Taybi Syndrome 66 0.028
148
ATT013 Attention Deficit-Hyperactivity Disorder 66 0.028
149
P ALP004 Alport Syndrome 66 0.028
150
P STH001 Saethre-Chotzen Syndrome 65 0.028
151
P FCL005 Focal Segmental Glomerulosclerosis 65 0.028
152
P PSD087 Pseudoxanthoma Elasticum 65 0.028
153
c HMP004 Hemophilia B 65 0.028
154
P FML011 Familial Adenomatous Polyposis 65 0.028
155
CNG034 Congestive Heart Failure 65 0.028
156
c HPT001 Hepatitis C 64 0.028
157
TBR010 Tuberculosis 64 0.028
158
P INF038 Influenza 64 0.028
159
INS024 Insulin-Like Growth Factor I 64 0.028
160
P GCH001 Gaucher's Disease 64 0.028
161
P MYL005 Myelofibrosis 64 0.028
162
c JVN010 Juvenile Rheumatoid Arthritis 64 0.028
163
P ESS003 Essential Thrombocythemia 63 0.028
164
c LKM062 Leukemia, Acute Lymphoblastic 63 0.028
165
c NMN015 Niemann-Pick Disease, Type C1 63 0.028
166
VNW001 Von Willebrand's Disease 63 0.028
167
P PND002 Pendred Syndrome 63 0.028
168
P BPL003 Bipolar Disorder 63 0.028
169
LYM115 Lymphoma, Non-Hodgkin 62 0.028
170
c SYS005 Systemic Scleroderma 62 0.028
171
P LKM068 Leukemia, Chronic Myeloid, Somatic 62 0.028
172
PLY125 Polycythemia Vera, Somatic 62 0.028
173
P VLC001 Velocardiofacial Syndrome 61 0.028
174
CRV047 Cervical Cancer, Somatic 61 0.028
175
P LPS004 Lupus Erythematosus 61 0.028
176
c GLY008 Glycogen Storage Disease Ii 61 0.028
177
P LYM007 Lymphangioleiomyomatosis 61 0.028
178
P ART022 Arthritis 61 0.028
179
P CTR001 Citrullinemia 61 0.028
180
P KDN017 Kidney Cancer 60 0.028
181
P AMY004 Amyloidosis 60 0.028
182
c HPT073 Hepatitis C Virus 60 0.028
183
MYC006 Mycosis Fungoides 60 0.028
184
MNT001 Mantle Cell Lymphoma 60 0.028
185
P EHL033 Ehlers-Danlos Syndrome, Classic Type 60 0.028
186
PLM001 Pulmonary Tuberculosis 60 0.028
187
P PLY014 Polycystic Kidney Disease 60 0.028
188
c BRD010 Bardet-Biedl Syndrome 1 59 0.028
189
c HPT016 Hepatitis B 59 0.028
190
BRN028 Brain Cancer 59 0.028
191
TYP007 Typhoid Fever 59 0.028
192
P NMN002 Niemann-Pick Disease 59 0.028
193
P CNT061 Conotruncal Heart Malformations 59 0.028
194
ALC007 Alcohol Dependence 59 0.028
195
P PLM036 Pulmonary Fibrosis 59 0.028
196
P HYP055 Hypoplastic Left Heart Syndrome 58 0.028
197
PRT036 Peritonitis 58 0.028
198
GST092 Gastroesophageal Reflux 58 0.028
199
ACR008 Acrocallosal Syndrome 58 0.028
200
P PLY011 Polycystic Ovary Syndrome 58 0.028
201
P SLV001 Silver-Russell Syndrome 58 0.028
202
BLD087 Bladder Cancer, Somatic 58 0.028
203
CRB039 Cerebrovascular Disease 58 0.028
204
P HLT001 Holt-Oram Syndrome 58 0.028
205
P LYM026 Lymphoblastic Leukemia 57 0.028
206
CFF002 Coffin-Lowry Syndrome 57 0.028
207
TWN003 Townes-Brocks Syndrome 57 0.028
208
ABT001 Abetalipoproteinemia 57 0.028
209
c BSL007 Basal Cell Carcinoma 57 0.028
210
P RTH001 Rothmund-Thomson Syndrome 57 0.028
211
MLG068 Malignant Glioma 57 0.028
212
P BCL006 B-Cell Lymphomas 57 0.028
213
MBS002 Moebius Syndrome 57 0.028
214
SRC014 Sarcoma 57 0.028
215
P ADN016 Adenocarcinoma 56 0.028
216
P PNM007 Pneumonia 56 0.028
217
OST085 Osteosarcoma, Somatic 56 0.028
218
OVR078 Ovarian Cancer, Somatic 56 0.028
219
P CRB019 Cerebral Amyloid Angiopathy 56 0.028
220
c GCH015 Gaucher Disease, Type I 56 0.028
221
IMG001 Image Syndrome 56 0.028
222
c SYS004 Systemic Mastocytosis 56 0.028
223
P PRM006 Primary Biliary Cirrhosis 56 0.028
224
P RCK004 Rickets 55 0.028
225
EWN003 Ewing Sarcoma 55 0.028
226
P AST007 Astrocytoma 55 0.028
227
P ANT006 Antiphospholipid Syndrome 55 0.028
228
ART016 Aortic Aneurysm 55 0.028
229
ACQ007 Acquired Immunodeficiency Syndrome 55 0.028
230
P ATR011 Atrial Fibrillation 55 0.028
231
SPN186 Spinal Cord Injury 55 0.028
232
VSC007 Vascular Disease 55 0.028
233
c MCL062 Mucolipidosis Ii Alpha/beta 55 0.028
234
CHR066 Chronic Fatigue Syndrome 55 0.028
235
P ORT004 Orthostatic Intolerance 55 0.028
236
SMT008 Smith-Magenis Syndrome 54 0.028
237
CRB037 Cerebral Palsy 54 0.028
238
PLM134 Pulmonary Fibrosis, Idiopathic 54 0.028
239
MVL001 Mevalonic Aciduria 54 0.028
240
P PRM011 Primary Ciliary Dyskinesia 54 0.028
241
PRP032 Porphyria Variegata 54 0.028
242
P MYL007 Myeloma 54 0.028
243
ADN018 Adenoma 54 0.028
244
P EPL002 Epilepsy Syndrome 54 0.028
245
EYD002 Eye Disease 54 0.028
246
MLN008 Melanoma 54 0.028
247
P ACR001 Aicardi-Goutieres Syndrome 53 0.028
248
ACN002 Acanthosis Nigricans 53 0.028
249
c ATM011 Autoimmune Hepatitis 53 0.028
250
HMT002 Hematologic Cancer 53 0.028
251
c FML001 Familial Atrial Fibrillation 53 0.028
252
DMN002 Dementia 53 0.028
253
P PLY018 Polycythemia 53 0.028
254
MLK003 Melkersson-Rosenthal Syndrome 53 0.028
255
P GLB002 Glioblastoma 53 0.028
256
PST028 Post-Traumatic Stress Disorder 53 0.028
257
RPP001 Rapp-Hodgkin Syndrome 53 0.028
258
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 53 0.028
259
IRR002 Irritable Bowel Syndrome 53 0.028
260
CHR020 Chronic Interstitial Cystitis 53 0.028
261
PLS007 Plasmodium Falciparum Malaria 52 0.028
262
GLB015 Glioblastoma Multiforme 52 0.028
263
HCL001 Hcl-V 52 0.028
264
P HRD011 Hereditary Spherocytosis 52 0.028
265
P MSC005 Muscular Dystrophy 52 0.028
266
PRP025 Peripheral Primitive Neuroectodermal Tumor 52 0.028
267
P INF032 Infertility 52 0.028
268
ETN001 Eating Disorder 52 0.028
269
c LCL006 Localized Scleroderma 52 0.028
270
c CNT035 Central Nervous System Disease 52 0.028
271
P EHL001 Ehlers-Danlos Syndrome 51 0.028
272
ART021 Arteriosclerosis 51 0.028
273
P DGR001 Digeorge Syndrome 51 0.028
274
P OST009 Osteochondritis Dissecans 51 0.028
275
c PRC016 Pre-Eclampsia 51 0.028
276
ICH002 Ichthyosis Bullosa of Siemens 51 0.028
277
P ESP024 Esophagitis 51 0.028
278
P PNC044 Pancreatitis 51 0.028
279
PLM129 Pulmonary Disease, Chronic Obstructive 51 0.028
280
HST011 Histoplasmosis 51 0.028
281
OCC006 Occipital Horn Syndrome 50 0.028
282
c ACT075 Acute Myocardial Infarction 50 0.028
283
ATH003 Atherosclerosis 50 0.028
284
HYP066 Hyperglycemia 50 0.028
285
VHW001 Vohwinkel Syndrome 50 0.028
286
MLL005 Miller-Dieker Syndrome 50 0.028
287
PRS047 Prostatitis 50 0.028
288
c EXD008 Exudative Vitreoretinopathy 1 50 0.028
289
VRL011 Viral Infectious Disease 50 0.028
290
HPY002 H. Pylori Infection 50 0.028
291
P ABD003 Abdominal Aortic Aneurysm 50 0.028
292
HYP056 Hypoglycemia 49 0.028
293
TRC008 Trachoma 49 0.028
294
P SNS014 Sinusitis 49 0.028
295
KRT001 Keratoconjunctivitis Sicca 49 0.028
296
CMP002 Campylobacteriosis 49 0.028
297
BRN012 Bronchiolitis Obliterans 49 0.028
298
c THR092 Thrombophilia Due to Thrombin Defect 49 0.028
299
ACT049 Acute Disseminated Encephalomyelitis 49 0.028
300
LKM067 Leukemia, Acute Promyelocytic, Somatic 49 0.028
301
ATX019 Ataxia with Vitamin E Deficiency 49 0.028
302
KRT002 Keratomalacia 49 0.028
303
MGR028 Migraine with or Without Aura 1 49 0.028
304
P THY032 Thyroiditis 48 0.028
305
LYM040 Lymphoblastic Lymphoma 48 0.028
306
LPM004 Lipoma 48 0.028
307
P NPH009 Nephrolithiasis 48 0.028
308
PRT103 Protoporphyria, Erythropoietic, Autosomal Recessive 48 0.028
309
P THR005 Thrombotic Thrombocytopenic Purpura 48 0.028
310
BRN002 Bronchiolitis 48 0.028
311
ART111 Artery Disease 48 0.028
312
NRT001 Neurotic Disorder 48 0.028
313
P LYM025 Lymphedema 48 0.028
314
DFF005 Diffuse Large B-Cell Lymphoma 48 0.028
315
P NRP001 Neuropathy 48 0.028
316
c SCN006 Secondary Syphilis 48 0.028
317
P ACT074 Acute Lymphocytic Leukemia 48 0.028
318
P CTR002 Cataract 48 0.028
319
P MST009 Mastocytosis 48 0.028
320
OCL001 Ocular Albinism 47 0.028
321
LYM019 Lymphosarcoma 47 0.028
322
MGL001 Megaloblastic Anemia 47 0.028
323
P PRS038 Personality Disorder 47 0.028
324
ISC004 Ischemia 47 0.028
325
P PRC031 Preeclampsia/eclampsia 1 47 0.028
326
CYT008 Cytomegalovirus Infection 47 0.028
327
P MCR115 Microvascular Complications of Diabetes 5 47 0.028
328
c CNG124 Congenital Rubella 47 0.028
329
P ECL001 Eclampsia 47 0.028
330
P RNL028 Renal Tubular Dysgenesis 47 0.028
331
ALL009 Allergic Conjunctivitis 46 0.028
332
P INT066 Interstitial Lung Disease 46 0.028
333
P SLP006 Sleep Apnea 46 0.028
334
P SPR013 Spiradenoma 46 0.028
335
RLP002 Relapsing-Remitting Multiple Sclerosis 46 0.028
336
OBS061 Obstructive Sleep Apnea 46 0.028
337
ORL004 Oral Submucous Fibrosis 46 0.028
338
P FML035 Familial Hyperlipidemia 46 0.028
339
P LRY016 Laryngeal Carcinoma 46 0.028
340
GST037 Gastroparesis 46 0.028
341
P LRY019 Laryngitis 46 0.028
342
IDP011 Idiopathic Interstitial Pneumonia 46 0.028
343
EVN001 Evans' Syndrome 46 0.028
344
PRD019 Periodic Fever, Familial 46 0.028
345
SPN020 Spondylosis 46 0.028
346
c INF069 Infantile Neuroaxonal Dystrophy 1 46 0.028
347
STF001 Stiff-Person Syndrome 46 0.028
348
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 0.028
349
c MCR113 Microvascular Complications of Diabetes 3 46 0.028
350
LPD008 Lipid Metabolism Disorder 45 0.028
351
P EPN002 Ependymoma 45 0.028
352
c ALM001 Al Amyloidosis 45 0.028
353
P MST018 Mesothelioma 45 0.028
354
GLS001 Gliosarcoma 45 0.028
355
CHL068 Cholestasis 45 0.028
356
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 45 0.028
357
CRD119 Cardiac Arrest 45 0.028
358
GST033 Gestational Diabetes 45 0.028
359
CRS005 Crest Syndrome 45 0.028
360
P ATR001 Atrioventricular Septal Defect 45 0.028
361
BLR001 Biliary Atresia 44 0.028
362
P FNC044 Fanconi Anemia, Complementation Group C 44 0.028
363
P CNT005 Central Nervous System Lymphoma 44 0.028
364
P MYS033 Miyoshi Muscular Dystrophy 1 44 0.028
365
PRL019 Prolidase Deficiency 44 0.028
366
P VSC005 Vesicoureteral Reflux 44 0.028
367
ACT008 Actinic Keratosis 44 0.028
368
GRF001 Graft-Versus-Host Disease, Protection Against 44 0.028
369
SML019 Smallpox 44 0.028
370
c INS002 in Situ Carcinoma 44 0.028
371
P PRC048 Precursor B-Cell Acute Lymphoblastic Leukemia 44 0.028
372
VNB005 Van Buchem Disease 44 0.028
373
CRT049 Critical Limb Ischemia 44 0.028
374
CNS004 Constipation 44 0.028
375
CHR285 Chronic Myelomonocytic Leukemia 44 0.028
376
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 44 0.028
377
P HML001 Hemolytic-Uremic Syndrome 44 0.028
378
GMM002 Gamma Chain Deficiency 44 0.028
379
P NRV006 Nervous System Cancer 44 0.028
380
VGN023 Vaginitis 44 0.028
381
NRN004 Neuroendocrine Tumor 44 0.028
382
P ACT135 Acute Graft Versus Host Disease 44 0.028
383
KRT009 Keratosis 43 0.028
384
P CLL015 Collagen Disease 43 0.028
385
TXC002 Toxic Encephalopathy 43 0.028
386
SCT005 Scott Syndrome 43 0.028
387
SML033 Small Cell Cancer of the Lung, Somatic 43 0.028
388
BRN106 Burns 43 0.028
389
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 43 0.028
390
c MLG079 Malignant Pleural Mesothelioma 43 0.028
391
ANR040 Aneurysm 43 0.028
392
P OTS001 Otosclerosis 43 0.028
393
P DNR001 Duane Retraction Syndrome 43 0.028
394
CMP004 Complement Factor I Deficiency 43 0.028
395
MCR004 Macroglobulinemia 43 0.028
396
c PND001 Pain Disorder 43 0.028
397
RCT018 Rectal Neoplasm 43 0.028
398
ORL011 Oral Cancer 43 0.028
399
P GLM040 Glioma Susceptibility 1 43 0.028
400
TRM010 Traumatic Brain Injury 43 0.028
401
NRC020 Neuroectodermal Tumor 43 0.028
402
GST050 Gastrointestinal System Disease 43 0.028
403
IPX001 Ipex Syndrome 43 0.028
404
NPH018 Nephrogenic Systemic Fibrosis 43 0.028
405
c PLY026 Polycystic Kidney Disease, Autosomal Dominant 43 0.028
406
GNT002 Giant Cell Glioblastoma 43 0.028
407
RTN023 Retinitis 43 0.028
408
GNG012 Gingival Overgrowth 43 0.028
409
MSM001 Meesmann Corneal Dystrophy 42 0.028
410
HYP266 Hypoxia 42 0.028
411
DRY001 Dry Eye Syndrome 42 0.028
412
FCT001 Factor Viii Deficiency 42 0.028
413
BRN071 Brain Injury 42 0.028
414
P CRV039 Cervicitis 42 0.028
415
HDC001 Headache 42 0.028
416
AND010 Androgen Insensitivity, Partial, with or Without Breast Cancer 42 0.028
417
LMT001 Limited Scleroderma 42 0.028
418
P BRN009 Burning Mouth Syndrome 42 0.028
419
P SCL009 Sclerosing Cholangitis 42 0.028
420
EBS001 Ebstein Anomaly 42 0.028
421
KLD001 Keloids 42 0.028
422
MCR165 Microphthalmia with Limb Anomalies 42 0.028
423
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.028
424
TLN003 Telangiectasis 41 0.028
425
c FML058 Familial Dilated Cardiomyopathy 41 0.028
426
PNM008 Pneumothorax 41 0.028
427
DCT002 Ductal Carcinoma in Situ 41 0.028
428
NTR005 Nutritional Deficiency Disease 41 0.028
429
P GND004 Gonadal Dysgenesis 41 0.028
430
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 41 0.028
431
SPN035 Spindle Cell Sarcoma 41 0.028
432
LFT009 Left Ventricular Outflow Tract Obstruction 41 0.028
433
STR026 Star Syndrome 41 0.028
434
c MCR129 Microvascular Complications of Diabetes 1 41 0.028
435
EWN002 Ewing's Family of Tumors 41 0.028
436
URT001 Urethritis 40 0.028
437
TRN060 Truncus Arteriosus 40 0.028
438
P VSC013 Visceral Heterotaxy 40 0.028
439
P PRP023 Peripheral Neuropathy 40 0.028
440
c BPL002 Bipolar I Disorder 40 0.028
441
CRK001 Cork-Handlers' Disease 40 0.028
442
CTN017 Cutaneous Necrotizing Vasculitis 40 0.028
443
CHL018 Childhood Medulloblastoma 40 0.028
444
CHR005 Chorioamnionitis 40 0.028
445
NRN002 Neuronitis 40 0.028
446
DFF035 Diffuse Cutaneous Systemic Sclerosis 40 0.028
447
BCT015 Bacteremia 40 0.028
448
DNN002 Donnai-Barrow Syndrome 39 0.028
449
c CHR092 Chronic Myeloproliferative Disease 39 0.028
450
TRN044 Transposition of the Great Arteries 39 0.028
451
CRT013 Carotid Stenosis 39 0.028
452
SPN051 Spondylitis 39 0.028
453
MNT002 Mental Depression 39 0.028
454
OCL020 Ocular Cicatricial Pemphigoid 39 0.028
455
BRX001 Bruxism 39 0.028
456
P CHR345 Chronic Pain 39 0.028
457
MNN014 Mononeuritis 39 0.028
458
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.028
459
P EHL015 Ehlers-Danlos Syndrome Progeroid Type 39 0.028
460
P CHL066 Cholangitis 39 0.028
461
DFF003 Diffuse Scleroderma 39 0.028
462
CRP017 Carpal Tunnel Syndrome, Familial 39 0.028
463
NCT008 Nicotine Dependence, Protection Against 39 0.028
464
MNG001 Mongolian Spot 39 0.028
465
MCL027 Macular Dystrophy, Dominant Cystoid 39 0.028
466
IND002 Indolent Systemic Mastocytosis 39 0.028
467
HTR003 Heterotaxy 38 0.028
468
LMB062 Limb Ischemia 38 0.028
469
IMN002 Iminoglycinuria, Digenic 38 0.028
470
CCN002 Cocaine Abuse 38 0.028
471
NRR001 Neuroretinitis 38 0.028
472
NPH010 Nephrosclerosis 38 0.028
473
GLM011 Glomerulosclerosis 38 0.028
474
CRB009 Cerebritis 37 0.028
475
c HMC010 Hemochromatosis, Type 3 37 0.028
476
DBT006 Diabetic Macular Edema 37 0.028
477
MYX001 Myxopapillary Ependymoma 37 0.028
478
HYP457 Hypertrophic Scars 37 0.028
479
GMS001 Gemistocytic Astrocytoma 37 0.028
480
FND002 Fundus Dystrophy 37 0.028
481
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 37 0.028
482
CHR008 Choroiditis 37 0.028
483
SML020 Small Patella Syndrome 37 0.028
484
c SVR056 Severe Hemophilia a 37 0.028
485
PPL001 Papillary Adenoma 36 0.028
486
PNC033 Pancreas Adenocarcinoma 36 0.028
487
c BSL024 Basal Cell Carcinoma 1 36 0.028
488
c PLY059 Polycystic Kidney Disease, Adult Type I 36 0.028
489
PLM005 Pleomorphic Lipoma 36 0.028
490
GRN017 Granulocytopenia 36 0.028
491
GLC022 Glucose/galactose Malabsorption 36 0.028
492
CRR007 Cirrhosis, Cryptogenic 36 0.028
493
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 36 0.028
494
PNM010 Pneumothorax, Primary Spontaneous 35 0.028
495
SPR008 Supratentorial Primitive Neuroectodermal Tumor 35 0.028
496
ORL012 Oral Leukoplakia 35 0.028
497
TCL003 T Cell Deficiency 35 0.028
498
BNT003 Bent Bone Dysplasia Syndrome 35 0.028
499
c FML169 Familial Osteochondritis Dissecans 35 0.028
500
P TRC087 Tricuspid Valve Disease 35 0.028
501
c FML305 Familial Abdominal Aortic Aneurysm 34 0.028
502
PMP002 Pemphigoid Gestationis 34 0.028
503
MCL006 Macular Retinal Edema 34 0.028
504
HRT007 Heart Cancer 34 0.028
505
ENT001 Enterocele 34 0.028
506
PRP021 Peripheral Nervous System Neoplasm 34 0.028
507
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.028
508
URT031 Ureteral Disease 34 0.028
509
P ATR010 Atrial Heart Septal Defect 34 0.028
510
TLS001 Tolosa-Hunt Syndrome 34 0.028
511
URN009 Urinary System Disease 33 0.028
512
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 33 0.028
513
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 33 0.028
514
OVR094 Ovarian Epithelial Cancer 33 0.028
515
CLB026 Colobomatous Microphthalmia 33 0.028
516
VTR005 Vitreous Disease 33 0.028
517
TMP011 Temple-Baraitser Syndrome 33 0.028
518
PLC008 Placenta Disease 33 0.028
519
c MTR002 Mitral Valve Insufficiency 32 0.028
520
LKP003 Leukoplakia 32 0.028
521
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 32 0.028
522
EXS013 Exstrophy-Epispadias Complex 32 0.028
523
c BNG032 Benign Mesothelioma 32 0.028
524
SPS004 Spastic Quadriplegia 32 0.028
525
c CRN159 Craniosynostosis, Type 1 32 0.028
526
VRL002 Variola Minor 31 0.028
527
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 31 0.028
528
c MLG049 Malignant Syringoma 31 0.028
529
TND004 Tendinopathy 31 0.028
530
MVM001 Movement Disease 31 0.028
531
RTC003 Root Caries 31 0.028
532
P ATX010 Ataxia Neuropathy Spectrum 31 0.028
533
PLY004 Polyp of Corpus Uteri 31 0.028
534
TND005 Tendinitis 31 0.028
535
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.028
536
c CHR064 Chronic Monocytic Leukemia 30 0.028
537
c CHL119 Cholangitis, Primary Sclerosing 30 0.028
538
c ARC016 Auriculocondylar Syndrome 1 30 0.028
539
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.028
540
DPH006 Diaphragmatic Eventration 30 0.028
541
c THR090 Thrombocythemia 1 30 0.028
542
P CRD132 Cardiac Conduction Defect 29 0.028
543
HRP007 Harp Syndrome 29 0.028
544
c HRD009 Hereditary Wilms' Tumor 29 0.028
545
BLR007 Biliary Tract Neoplasm 29 0.028
546
P PLM040 Pulmonary Valve Disease 28 0.028
547
c THR037 Thrombocytopenia 2 28 0.028
548
CRN244 Corneal Dystrophy, Schnyder Type 28 0.028
549
c PSR017 Psoriasis 2 28 0.028
550
P PSR004 Psoriasis Susceptibility 1 28 0.028
551
ACT118 Acute Non Lymphoblastic Leukemia 28 0.028
552
ATN003 Autonomic Nervous System Neoplasm 28 0.028
553
P PLM071 Pulmonary Surfactant Metabolism Dysfunction 28 0.028
554
LWC001 Low Compliance Bladder 28 0.028
555
MTL002 Metal Metabolism Disorder 28 0.028
556
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 27 0.028
557
c LYM110 Lymphedema, Hereditary, Ia 27 0.028
558
CHP002 Chops Syndrome 27 0.028
559
SNY001 Snyder-Robinson Syndrome 27 0.028
560
c CNT058 Central Nervous System Lymphoma, Primary 27 0.028
561
MNT054 Mental Retardation, X-Linked, Snyder-Robinson Type 27 0.028
562
PNG002 Pain Agnosia 26 0.028
563
CHL013 Cholecystolithiasis 26 0.028
564
CL1004 Col1a1/2-Related Osteogenesis Imperfecta 26 0.028
565
RHM007 Rheumatic Congestive Heart Failure 26 0.028
566
KDN013 Kidney Hypertrophy 26 0.028
567
OCL011 Ocular Motility Disease 26 0.028
568
P PRX010 Paroxysmal Ventricular Fibrillation 26 0.028
569
CPL005 Capillary Disease 26 0.028
570
P FNC026 Fanconi Renotubular Syndrome 1 26 0.028
571
LNG015 Lingual-Facial-Buccal Dyskinesia 26 0.028
572
MNN028 Mononeuropathy of the Median Nerve, Mild 26 0.028
573
NNT011 Neonatal Anemia 25 0.028
574
c MCR120 Microvascular Complications of Diabetes 7 25 0.028
575
NRC003 Narcissistic Personality Disorder 25 0.028
576
MLD004 Mal De Debarquement 25 0.028
577
ADR023 Adrenomyodystrophy 25 0.028
578
PRM087 Premature Chromatid Separation Trait 24 0.028
579
c THR087 Thrombocythemia 2 24 0.028
580
MNG003 Mungan Syndrome 24 0.028
581
SPR101 Superior Semicircular Canal Dehiscence Syndrome 24 0.028
582
ANP019 Anophthalmos with Limb Anomalies 23 0.028
583
c PSR019 Psoriasis Susceptibility 13 23 0.028
584
c ACT219 Acute Myeloid Leukemia, Flt3-Related 23 0.028
585
P NRB002 Neuroblastoma, Susceptibility 23 0.028
586
GRN008 Granular Cell Carcinoma 23 0.028
587
c LNG072 Lung Cancer Susceptibility 2 23 0.028
588
c MCR130 Microvascular Complications of Diabetes 6 23 0.028
589
SNG009 Single Ventricular Septal Defect 22 0.028
590
c SCN044 Secondary Ciliary Dyskinesia 22 0.028
591
c MCR112 Microvascular Complications of Diabetes 2 22 0.028
592
MLT104 Multiple Benign Circumferential Skin Creases on Limbs 22 0.028
593
RFR002 Refractory Hairy Cell Leukemia 21 0.028
594
c SBC039 Subacute Cerebellar Degeneration 21 0.028
595
P HRT017 Heart Tumor 21 0.028
596
ADL087 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia 21 0.028
597
PSR005 Psoriasis, Protection Against 21 0.028
598
c MCR133 Microvascular Complications of Diabetes 4 21 0.028
599
PRS063 Paresthesia 20 0.028
600
TMR013 Tumor Necrosis Factor Receptor 1 Associated Periodic Syndrome 20 0.028
601
P ACT080 Acute Pulmonary Heart Disease 20 0.028
602
DSS022 Disseminated Peritoneal Leiomyomatosis 20 0.028
603
c THR086 Thrombocythemia 3 19 0.028
604
AND005 Androgen Insensitivity Syndrome, Mild 19 0.028
605
PLL005 Pallister-Killian Mosaic Syndrome 18 0.028
606
ICH056 Ichthyosis-Hypotrichosis Syndrome 18 0.028
607
FML045 Familial Mosaic Monosomy 7 Syndrome 17 0.028
608
SBC016 Subacute Delirium 15 0.028
609
IDP020 Idiopathic Juxtafoveal Retinal Telangiectasia 15 0.028
610
c RHN011 Rh-Null Regulator Type Related Hemolytic Anemia 14 0.028
611
c ALK004 Alk-Related Neuroblastoma Susceptibility 14 0.028
612
CNG422 Congenitally Uncorrected Transposition of the Great Arteries 13 0.028
613
TRN013 Transient Neonatal Thrombocytopenia 12 0.028
614
PGM008 Pigmentary Cirrhosis 10 0.028
615
c ADL079 Adult Heart Tumor 7 0.028
616
HRT029 Heart Tumor of the Child 7 0.028