Search results for lymphoproliferative syndrome

634 hits were found for lymphoproliferative syndrome

# Family MCID Name MIFTS Score
1
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 7.768
2
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 51 7.105
3
c ATM030 Autoimmune Lymphoproliferative Syndrome, Type Ii 32 4.714
4
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 30 4.694
5
RSS025 Ras-Associated Autoimmune Leukoproliferative Disorder 41 4.691
6
c LYM114 Lymphoproliferative Syndrome, X-Linked, 2 43 4.689
7
P LYM033 Lymphoproliferative Syndrome 56 4.376
8
c ATM046 Autoimmune Lymphoproliferative Syndrome, Type Iib 37 4.295
9
c LYM107 Lymphoproliferative Syndrome 2 50 4.126
10
c ATM083 Autoimmune Lymphoproliferative Syndrome, Type Iii 38 4.045
11
c LYM106 Lymphoproliferative Syndrome 1 32 3.859
12
DNZ002 Dianzani Autoimmune Lymphoproliferative Disease 10 3.646
13
c ATM087 Autoimmune Lymphoproliferative Syndrome Due to Ctla4 Haploinsuffiency 10 3.238
14
c PRK077 Prkcd-Related Autoimmune Lymphoproliferative Syndrome 12 2.478
15
c ATS229 Autosomal Recessive Lymphoproliferative Disease 19 1.976
16
IGG007 Igg4-Related Disease 38 1.549
17
LYM054 Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 4 1.453
18
c ATM027 Autoimmune Lymphoproliferative Syndrome, Type 0 11 1.442
19
c CSP002 Casp10-Related Autoimmune Lymphoproliferative Syndrome 7 1.440
20
c FSL002 Faslg-Related Autoimmune Lymphoproliferative Syndrome 7 1.440
21
c FSR002 Fas-Related Autoimmune Lymphoproliferative Syndrome 7 1.440
22
P LYM118 Lymphoma 69 0.323
23
PST046 Post-Transplant Lymphoproliferative Disease 54 0.287
24
P LKM002 Leukemia 71 0.240
25
ADL002 Adult Syndrome 52 0.182
26
LYM024 Lymphatic System Disease 52 0.175
27
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.172
28
P HPT021 Hepatitis 69 0.160
29
LYM023 Lymphatic System Cancer 33 0.152
30
KDS001 Kid Syndrome 53 0.151
31
CHL071 Child Syndrome 58 0.150
32
MYL009 Myelodysplastic Syndrome 73 0.144
33
P BCL006 B-Cell Lymphomas 65 0.144
34
IMM136 Immune System Disease 51 0.140
35
C3D001 C3 Deficiency 53 0.137
36
LYM019 Lymphosarcoma 53 0.135
37
c CHR090 Chronic Lymphocytic Leukemia 76 0.132
38
HDG012 Hodgkin Lymphoma 77 0.129
39
CRB009 Cerebritis 39 0.129
40
c ADL001 Adult Lymphoma 39 0.128
41
ALR002 Al-Raqad Syndrome 36 0.128
42
P ART022 Arthritis 75 0.128
43
P LYM026 Lymphoblastic Leukemia 62 0.124
44
INC022 Inclusion-Cell Disease 46 0.120
45
WLL006 Wells Syndrome 59 0.120
46
HMT018 Hematopoietic Stem Cell Transplantation 41 0.120
47
AND005 Androgen Insensitivity Syndrome, Mild 16 0.119
48
P THR014 Thrombocytopenia 64 0.116
49
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.116
50
LYM067 Lymphoid Leukemia 44 0.115
51
c CHR418 Chronic Leukemia 47 0.114
52
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.112
53
GDS001 Good Syndrome 44 0.112
54
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.109
55
P RHM011 Rheumatoid Arthritis 89 0.108
56
LYM051 Lymphomatoid Granulomatosis 47 0.107
57
HPT074 Hepatic Adenoma, Somatic 50 0.107
58
LYM115 Lymphoma, Non-Hodgkin 63 0.107
59
P WSK001 Wiskott-Aldrich Syndrome 73 0.106
60
VSC011 Vasculitis 62 0.106
61
HNM002 Hinman Syndrome 25 0.106
62
MYC006 Mycosis Fungoides 66 0.105
63
c ACT073 Acute Leukemia 60 0.103
64
PLS011 Plasmacytoma 56 0.103
65
P ANP001 Anaplastic Large Cell Lymphoma 57 0.103
66
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.101
67
CMM004 Common Variable Immunodeficiency 68 0.101
68
P EPL164 Epilepsy 66 0.100
69
c LKM004 Leukemia, B-Cell, Chronic 24 0.099
70
CSY001 C Syndrome 50 0.099
71
P LPS004 Lupus Erythematosus 64 0.099
72
BLD054 Blood Protein Disease 37 0.098
73
SPL018 Splenomegaly 44 0.098
74
VRL011 Viral Infectious Disease 55 0.098
75
P HYP098 Hypereosinophilic Syndrome 63 0.097
76
P FTL001 Fetal Alcohol Syndrome 53 0.097
77
c SYS001 Systemic Lupus Erythematosus 86 0.097
78
DFF005 Diffuse Large B-Cell Lymphoma 59 0.095
79
MRG013 Mirage Syndrome 29 0.095
80
P PNM007 Pneumonia 68 0.095
81
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.095
82
P TCL004 T-Cell Leukemia 47 0.094
83
P APL001 Aplastic Anemia 75 0.094
84
P ENC018 Encephalopathy 59 0.094
85
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.093
86
c PRM023 Pre-Malignant Neoplasm 41 0.093
87
LKC003 Leukocyte Disease 43 0.092
88
LYM052 Lymphomatoid Papulosis 41 0.092
89
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.092
90
THR024 Thrombosis 57 0.091
91
THR013 Thoracic Outlet Syndrome 50 0.091
92
P MYL006 Myeloid Leukemia 66 0.090
93
P PNC044 Pancreatitis 61 0.089
94
PRP030 Purpura 58 0.089
95
P BLD051 Blood Coagulation Disease 42 0.089
96
SPL012 Splenic Disease 46 0.088
97
c ADL017 Adult T-Cell Leukemia 60 0.088
98
VSC008 Vascular Hemostatic Disease 30 0.088
99
PRP036 Peripheral T-Cell Lymphoma 45 0.088
100
BNM001 Bone Marrow Cancer 51 0.088
101
P HMR003 Hemorrhagic Disease 57 0.087
102
BLD053 Blood Platelet Disease 46 0.086
103
SRC014 Sarcoma 66 0.086
104
P MLT019 Multiple Myeloma 83 0.086
105
P HML002 Hemolytic Anemia 62 0.086
106
CRD118 Cardiovascular Cancer 44 0.086
107
MTH049 Methotrexate-Associated Lymphoproliferative Disorders 17 0.086
108
END072 Endotheliitis 42 0.085
109
VSC006 Vascular Cancer 51 0.085
110
c HPT001 Hepatitis C 68 0.085
111
P GLM007 Glomerulonephritis 59 0.085
112
MCR004 Macroglobulinemia 50 0.084
113
MNT001 Mantle Cell Lymphoma 72 0.084
114
ACD009 Acid-Labile Subunit, Deficiency of 45 0.084
115
HMT002 Hematologic Cancer 64 0.084
116
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.083
117
HRY003 Hairy Cell Leukemia 57 0.083
118
P HYP055 Hypoplastic Left Heart Syndrome 61 0.082
119
CRY004 Cryoglobulinemia 46 0.082
120
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.081
121
SZR001 Sezary's Disease 52 0.081
122
P NRP001 Neuropathy 59 0.081
123
PLS009 Plasma Cell Neoplasm 48 0.080
124
BRT030 Birth Defects 43 0.080
125
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.080
126
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.079
127
PRM243 Primary Bone Cancer 29 0.078
128
ACT118 Acute Non Lymphoblastic Leukemia 30 0.078
129
c ATM011 Autoimmune Hepatitis 60 0.077
130
ACR041 Acromelic Frontonasal Dysostosis 45 0.077
131
RTC005 Reticulosarcoma 48 0.076
132
P CRV039 Cervicitis 45 0.076
133
c ATM010 Autoimmune Hemolytic Anemia 60 0.076
134
P HPT023 Hepatocellular Carcinoma 92 0.076
135
P INT068 Intestinal Disease 60 0.076
136
MRG003 Marginal Zone B-Cell Lymphoma 52 0.076
137
P SCK002 Sick Sinus Syndrome 50 0.075
138
SPL011 Spleen Cancer 36 0.075
139
P SJG001 Sjogren's Syndrome 50 0.075
140
RFR004 Refractory Hematologic Cancer 28 0.074
141
PRR002 Pure Red-Cell Aplasia 47 0.074
142
P FLL037 Follicular Lymphoma 70 0.074
143
SVR004 Severe Combined Immunodeficiency 69 0.074
144
P PFF001 Pfeiffer Syndrome 73 0.074
145
LYM040 Lymphoblastic Lymphoma 53 0.074
146
SKN016 Skin Disease 66 0.074
147
P AMY004 Amyloidosis 65 0.074
148
P NTR004 Neutropenia 59 0.074
149
LRN003 Learning Disability 49 0.074
150
MTH009 Mouth Disease 61 0.073
151
ALL026 Allergic Hypersensitivity Disease 52 0.073
152
DFC004 Deficiency Anemia 64 0.073
153
P DGR001 Digeorge Syndrome 53 0.073
154
RTC009 Reticulum Cell Sarcoma 47 0.073
155
P ENC004 Encephalitis 63 0.072
156
PLS025 Plasmablastic Lymphoma 46 0.072
157
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.072
158
FML039 Female Reproductive System Disease 48 0.072
159
ATM012 Autoimmune Disease of Blood 35 0.072
160
P UVT001 Uveitis 58 0.072
161
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.071
162
ATM052 Autoimmune Disease 1 25 0.071
163
LYM104 Lymphoma, Malt, Somatic 54 0.070
164
c FLL041 Follicular Lymphoma 1 45 0.070
165
LYM012 Lymphoplasmacytic Lymphoma 44 0.070
166
STF001 Stiff-Person Syndrome 56 0.070
167
PLS016 Plasma Cell Leukemia 42 0.070
168
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.069
169
P WLD002 Waldenstrom Macroglobulinemia 58 0.069
170
SPL004 Splenic Marginal Zone Lymphoma 44 0.069
171
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.069
172
HDG004 Hodgkin's Granuloma 24 0.069
173
CHL061 Childhood Leukemia 49 0.069
174
P ACT074 Acute Lymphocytic Leukemia 56 0.069
175
HDG006 Hodgkin's Paragranuloma 17 0.069
176
NTR005 Nutritional Deficiency Disease 36 0.069
177
LMB002 Lambert-Eaton Myasthenic Syndrome 49 0.068
178
LYM116 Lymph Node Disease 47 0.068
179
c HPT073 Hepatitis C Virus 73 0.067
180
ATM053 Autoimmune Disease 2 16 0.067
181
BRK010 Burkitt Lymphoma 69 0.067
182
P PNC001 Pancytopenia 52 0.067
183
MLR004 Malaria 83 0.067
184
BNC003 Bone Cancer 58 0.067
185
CLL014 Cll/sll 42 0.066
186
LRG008 Large Granular Lymphocyte Leukemia 39 0.066
187
BNS002 Bone Structure Disease 37 0.066
188
PRM097 Primary Immunodeficiency Disease 60 0.066
189
ACQ017 Acquired Von Willebrand Syndrome 37 0.065
190
P BRS047 Breast Cancer 100 0.065
191
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.065
192
P CTN015 Cutaneous T Cell Lymphoma 50 0.065
193
RCH001 Richter's Syndrome 45 0.065
194
CLN019 Colonic Disease 51 0.065
195
P CNT005 Central Nervous System Lymphoma 53 0.065
196
EVN001 Evans' Syndrome 43 0.065
197
EPS006 Epstein Syndrome 38 0.064
198
c CHR064 Chronic Monocytic Leukemia 42 0.064
199
P CHR084 Chromosomal Disease 32 0.064
200
P MNN013 Meningitis 67 0.064
201
P LFR001 Li-Fraumeni Syndrome 75 0.064
202
DRM006 Dermatitis 66 0.064
203
CYT008 Cytomegalovirus Infection 52 0.064
204
TCL002 T-Cell Large Granular Lymphocyte Leukemia 42 0.064
205
c CRN214 Coronary Heart Disease 5 22 0.064
206
PRP027 Peripheral Vascular Disease 68 0.064
207
c LKM061 Leukemia, Acute Myeloid 73 0.063
208
c HPT016 Hepatitis B 64 0.063
209
NTR003 Natural Killer Cell Leukemia 47 0.063
210
P DRV001 Dravet Syndrome 69 0.063
211
NSY001 N Syndrome 36 0.063
212
LYM126 Lymphoma Aids Related 15 0.063
213
P ATX010 Ataxia Neuropathy Spectrum 30 0.063
214
P HST010 Histiocytosis 58 0.063
215
ALN001 Aland Island Eye Disease 45 0.063
216
TTR016 Tetra-Amelia Syndrome 36 0.062
217
P CRN178 Coronary Heart Disease 6 21 0.062
218
P FNC043 Fanconi Anemia, Complementation Group E 55 0.062
219
PCK002 Pick Disease 68 0.062
220
PHY002 Physical Disorder 43 0.062
221
DDX002 Ddx41-Related Susceptibility to Familial Myeloproliferative/lymphoproliferative Neoplasms 13 0.061
222
RBR001 Roberts Syndrome 60 0.061
223
ATM055 Autoimmune Disease 4 15 0.061
224
P CLR023 Colorectal Cancer 97 0.061
225
CLT003 Colitis 60 0.061
226
c LKM005 Leukemia, T-Cell, Chronic 20 0.061
227
OCL009 Ocular Cancer 59 0.061
228
c LKM062 Leukemia, Acute Lymphoblastic 64 0.061
229
c CRN173 Coronary Heart Disease 8 18 0.061
230
RPR002 Reproductive System Disease 41 0.061
231
KPS004 Kaposi Sarcoma 67 0.060
232
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.060
233
PLS003 Plasmacytic Leukemia 21 0.060
234
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.060
235
c ACT020 Acute T Cell Leukemia 35 0.060
236
GRY002 Gray Platelet Syndrome 55 0.060
237
HRT007 Heart Cancer 46 0.060
238
P HRT017 Heart Tumor 32 0.060
239
c ADL079 Adult Heart Tumor 16 0.059
240
BNL002 Bone Lymphoma 32 0.059
241
P PLY019 Polyneuropathy 56 0.059
242
ATM054 Autoimmune Disease 3 15 0.059
243
INT051 Intussusception 50 0.058
244
P KDN018 Kidney Disease 66 0.058
245
P LVR013 Liver Disease 75 0.058
246
MDS022 Mediastinitis 41 0.058
247
P MYL005 Myelofibrosis 67 0.057
248
P NJM001 Nijmegen Breakage Syndrome 67 0.057
249
PNN001 Panniculitis 51 0.057
250
HDC001 Headache 54 0.057
251
P KDN017 Kidney Cancer 65 0.057
252
ATM059 Autoimmune Disease 6 22 0.057
253
INT253 Intestinal Benign Neoplasm 47 0.056
254
SXL003 Sexual Disorder 42 0.056
255
P PLY017 Polyarteritis Nodosa 51 0.056
256
P ANG015 Angioedema 52 0.056
257
PRL017 Prolymphocytic Leukemia 47 0.056
258
P ESP024 Esophagitis 61 0.056
259
P GRN010 Granular Cell Tumor 47 0.056
260
P AST007 Astrocytoma 65 0.056
261
c CRN172 Coronary Heart Disease 3 19 0.055
262
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.055
263
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.055
264
c CRN175 Coronary Heart Disease 4 19 0.055
265
ADP007 Adie Pupil 34 0.055
266
ADJ001 Adjustment Disorder 38 0.055
267
APH001 Aphthous Stomatitis 62 0.055
268
GNG013 Gingivitis 61 0.055
269
c PRM226 Primary Central Nervous System Lymphoma 49 0.054
270
PRP019 Peripheral Nervous System Disease 55 0.054
271
P NRM001 Neuromyelitis Optica 60 0.054
272
P FND001 Fundus Albipunctatus 55 0.054
273
HYP063 Hypersplenism 48 0.054
274
TBR010 Tuberculosis 70 0.054
275
P AGM001 Agammaglobulinemia 64 0.054
276
GRW007 Growth Hormone Deficiency 50 0.053
277
BND014 Bone Development Disease 40 0.053
278
LYM127 Lymphatic Malformations 39 0.053
279
MYL031 Myeloproliferative Neoplasm 58 0.053
280
MLN008 Melanoma 62 0.052
281
STM007 Stomatitis 50 0.052
282
ATN002 Autonomic Nervous System Disease 48 0.052
283
LYM045 Lymphocytic Vasculitis 33 0.052
284
c ATM024 Autoimmune Pancreatitis 47 0.052
285
c FML303 Familial/multiple Cancer 14 0.052
286
PRM151 Primary Bone Lymphoma 26 0.052
287
MSL001 Measles 61 0.052
288
ACR002 Acrocapitofemoral Dysplasia 33 0.052
289
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.051
290
P CLC005 Celiac Disease 68 0.051
291
SPC003 Specific Developmental Disorder 38 0.051
292
HDG009 Hodgkin Lymphoma, Childhood 14 0.051
293
WLK001 Walker-Warburg Syndrome 52 0.051
294
OST017 Osteomyelitis 61 0.051
295
MNC004 Monoclonal Paraproteinemia 34 0.051
296
RFR010 Refractory Anemia 45 0.051
297
TNS005 Tonsillitis 57 0.051
298
P TRC086 Trichohepatoenteric Syndrome 1 48 0.051
299
c RNL016 Renal Infectious Disease 20 0.051
300
ABL002 Ablepharon-Macrostomia Syndrome 57 0.051
301
MSC004 Muscle Tissue Disease 34 0.051
302
c MCR162 Macroglobulinemia, Waldenstrom 2 17 0.051
303
P PRT013 Portal Hypertension 60 0.051
304
P FRD001 Friedreich Ataxia 62 0.050
305
HRT029 Heart Tumor of the Child 15 0.050
306
YNG002 Young Syndrome 26 0.050
307
SML025 Small Non-Cleaved Cell Lymphoma 22 0.050
308
P MSC007 Muscle Hypertrophy 58 0.050
309
MXD023 Mixed Cell Type Cancer 44 0.050
310
IMG001 Image Syndrome 50 0.050
311
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.050
312
STM006 Stomach Disease 50 0.050
313
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 0.049
314
P CHR562 Chronic Myelocytic Leukemia 41 0.049
315
CYS001 Cystic Fibrosis 83 0.049
316
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.049
317
HMN032 Human Herpesvirus 8 46 0.049
318
P NRV007 Nervous System Disease 71 0.049
319
P ASP006 Aspergillosis 61 0.049
320
CRB025 Carbohydrate Metabolic Disorder 46 0.049
321
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.049
322
RFR001 Refractory Plasma Cell Neoplasm 16 0.049
323
VND001 Vein Disease 47 0.048
324
P NRV006 Nervous System Cancer 60 0.048
325
MCS002 Mucositis 55 0.048
326
P SML016 Small Intestine Cancer 52 0.048
327
c TCL005 T-Cell Prolymphocytic Leukemia 52 0.048
328
LNR006 Linear Iga Disease 40 0.048
329
TCL019 T-Cell Childhood Lymphoblastic Lymphoma 14 0.048
330
P TXP001 Toxoplasmosis 61 0.048
331
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.047
332
c ACQ012 Acquired Angioedema 39 0.047
333
LYM004 Lymphoid Interstitial Pneumonia 33 0.047
334
ANG049 Angioedema Induced by Ace Inhibitors 34 0.047
335
P CFF001 Coffin-Siris Syndrome 51 0.047
336
NNH003 Non-Hodgkin Lymphoma, Childhood 12 0.047
337
P INF037 Inflammatory Bowel Disease 63 0.047
338
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 47 0.047
339
PRM026 Primary Systemic Mycosis 36 0.047
340
HPT022 Hepatoblastoma 55 0.047
341
P XLN007 X-Linked Disease 34 0.046
342
LYM048 Lymphoma, Large-Cell, Immunoblastic 25 0.046
343
SLD003 Sialadenitis 49 0.046
344
P MYC068 Myoclonic Epilepsy of Infancy 36 0.046
345
ORL011 Oral Cancer 56 0.046
346
P SKN013 Skin Benign Neoplasm 43 0.046
347
SPN051 Spondylitis 51 0.046
348
ADR038 Adermatoglyphia 46 0.046
349
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.046
350
P SZR006 Seizure Disorder 56 0.046
351
WHT007 White Platelet Syndrome 15 0.045
352
P MSC005 Muscular Dystrophy 65 0.045
353
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.045
354
RSD004 Rosai-Dorfman Disease 41 0.045
355
HST016 Histiocytic Sarcoma 40 0.045
356
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.045
357
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.045
358
CMP001 Composite Lymphoma 37 0.045
359
P RNL014 Renal Cell Carcinoma 82 0.045
360
P PRM019 Premature Ovarian Failure 64 0.045
361
P SPS003 Spastic Diplegia 52 0.045
362
DSS008 Disease of Mental Health 52 0.045
363
RNL007 Renal Tubular Acidosis 50 0.045
364
GST050 Gastrointestinal System Disease 56 0.045
365
c BNG076 Benign Exophthalmos Syndrome 15 0.045
366
P LCT001 Lactic Acidosis 51 0.044
367
PRP021 Peripheral Nervous System Neoplasm 46 0.044
368
P HRP006 Herpes Simplex 65 0.044
369
VRS001 Virus Associated Hemophagocytic Syndrome 35 0.044
370
FRB001 Farber Lipogranulomatosis 53 0.044
371
P MDL005 Medulloblastoma 77 0.044
372
FNC006 Functional Gastric Disease 32 0.043
373
NRT004 Neuritis 52 0.043
374
P ORL007 Oral Cavity Cancer 59 0.043
375
P THR015 Thrombophilia 59 0.043
376
SKN023 Skin Tag 44 0.043
377
P HYP097 Hyperekplexia 54 0.043
378
c INV001 Invasive Aspergillosis 47 0.043
379
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.043
380
HYP266 Hypoxia 56 0.043
381
WHM001 Whim Syndrome 53 0.043
382
LYM020 Lymph Node Cancer 39 0.043
383
BND002 B- and T-Cell Mixed Leukemia 17 0.043
384
ACT103 Acute Lymphoblastic Leukemia, Childhood 41 0.042
385
P MYS005 Myositis 57 0.042
386
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 29 0.042
387
LVR006 Liver Lymphoma 27 0.042
388
LYM041 Lymphocytes Absent 13 0.042
389
P EXN002 Exanthem 57 0.042
390
P HYP345 Hyper-Ige Recurrent Infection Syndrome 54 0.042
391
SFT003 Soft Tissue Sarcoma 57 0.042
392
ANG037 Angiomatosis 37 0.042
393
BCL002 B Cell Deficiency 49 0.042
394
TBR011 Tuberculous Meningitis 47 0.042
395
TCL003 T Cell Deficiency 45 0.042
396
P ACT135 Acute Graft Versus Host Disease 53 0.042
397
IPX001 Ipex Syndrome 45 0.042
398
CCN007 Cocoon Syndrome 45 0.042
399
LMY003 Leiomyomatosis 42 0.042
400
P DMY001 Demyelinating Polyneuropathy 43 0.041
401
P ATX030 Ataxia-Telangiectasia 77 0.041
402
P BCL005 B Cell Prolymphocytic Leukemia 43 0.041
403
BLS007 Blastic Plasmacytoid Dendritic Cell 41 0.041
404
INC021 Incontinentia Pigmenti 59 0.041
405
P PLY018 Polycythemia 58 0.041
406
c SRC023 Sarcoidosis 2 33 0.041
407
GST078 Gastrointestinal Allergy 40 0.041
408
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.041
409
RFR002 Refractory Hairy Cell Leukemia 29 0.041
410
c ALM001 Al Amyloidosis 49 0.041
411
P SNS014 Sinusitis 60 0.041
412
c TRC078 Trichohepatoenteric Syndrome 2 29 0.041
413
P PLY041 Polymyositis 52 0.040
414
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.040
415
ADT003 Auditory System Disease 40 0.040
416
P LDD002 Liddle Syndrome 53 0.040
417
PLC008 Placenta Disease 33 0.040
418
c ANP011 Anaplastic Small Cell Lymphoma 14 0.040
419
P KBK002 Kabuki Syndrome 1 49 0.040
420
P MNC007 Monocytic Leukemia 55 0.040
421
FDL002 Food Allergy 53 0.040
422
c CNT035 Central Nervous System Disease 60 0.039
423
c HMN022 Human T-Cell Leukemia Virus Type 2 44 0.039
424
LYM005 Lymphocele 35 0.039
425
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.039
426
NTR018 Neutrophilia, Hereditary 42 0.039
427
P DRM010 Dermatomyositis 62 0.039
428
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.039
429
CLD007 Cold Agglutinin Disease 44 0.039
430
P LPR003 Leprosy 69 0.039
431
P DYS007 Dyskeratosis Congenita 63 0.038
432
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.038
433
TMR010 Tumor Predisposition Syndrome 47 0.038
434
INT067 Interstitial Nephritis 46 0.038
435
SPN060 Spondylocarpotarsal Synostosis Syndrome 34 0.038
436
VSC009 Vascular Skin Disease 19 0.038
437
EXT010 Extramedullary Plasmacytoma 49 0.038
438
BRN022 Bronchiectasis 50 0.038
439
MLT001 Multiple Chemical Sensitivity 43 0.038
440
c FNC027 Fanconi Anemia, Complementation Group a 71 0.038
441
ECT004 Ecthyma 35 0.038
442
P ARC016 Auriculocondylar Syndrome 1 40 0.038
443
P GST044 Gastritis 56 0.037
444
CRB001 Cerebral Lymphoma 33 0.037
445
ATN003 Autonomic Nervous System Neoplasm 40 0.037
446
P MST009 Mastocytosis 56 0.037
447
P LMY004 Leiomyosarcoma 55 0.037
448
LCH009 Lichen Sclerosus 41 0.037
449
LSH001 Leishmaniasis 66 0.037
450
c LKM060 Leukemia, Acute Lymphoblastic 3 50 0.037
451
MMB001 Membranoproliferative Glomerulonephritis 46 0.037
452
GRN017 Granulocytopenia 44 0.037
453
PLM001 Pulmonary Tuberculosis 67 0.036
454
C1N001 C1 Inhibitor Deficiency 38 0.036
455
c ACT134 Acute Liver Failure 50 0.036
456
c HYP539 Hyperekplexia, Hereditary 1, Autosomal Dominant or Recessive 33 0.036
457
P MCR129 Microvascular Complications of Diabetes 1 54 0.036
458
OPT009 Optic Neuritis 50 0.036
459
HML018 Homologous Wasting Disease 13 0.036
460
OLG003 Oligohydramnios 53 0.036
461
MLY001 Molybdenum Cofactor Deficiency 38 0.036
462
PTY004 Pityriasis Lichenoides 23 0.036
463
c CLL013 Cell Type Cancer 46 0.036
464
ANG020 Angiosarcoma 53 0.035
465
APP015 Apparent Mineralocorticoid Excess 51 0.035
466
CRY005 Cryptococcosis 50 0.035
467
ATN004 Autonomic Neuropathy 45 0.035
468
ADR007 Adrenoleukodystrophy 72 0.035
469
TST021 Testicular Germ Cell Tumor 69 0.035
470
P DMN001 Diamond-Blackfan Anemia 69 0.035
471
VSC003 Visceral Leishmaniasis 56 0.035
472
CD4003 Cd40 Ligand Deficiency 46 0.035
473
c PRM225 Primary Thrombocytopenia 39 0.035
474
ARC008 Auriculo-Condylar Syndrome 30 0.035
475
c ATM007 Autoimmune Disease of Central Nervous System 25 0.035
476
NSP002 Nasopharyngitis 40 0.035
477
c CHR096 Chronic Pulmonary Heart Disease 40 0.035
478
CPL005 Capillary Disease 36 0.035
479
ACR005 Acrodermatitis 36 0.035
480
LTH001 Lethal Midline Granuloma 37 0.035
481
ANP010 Anaplastic Plasmacytoma 19 0.035
482
MGR028 Migraine with or Without Aura 1 47 0.034
483
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.034
484
c THR037 Thrombocytopenia 2 35 0.034
485
MNT045 Montefiore Syndrome 10 0.034
486
P GLY010 Glycine Encephalopathy 53 0.034
487
c TYP024 Type Ii Mixed Cryoglobulinemia 33 0.034
488
PRM128 Primary Cutaneous Follicle Center Lymphoma 26 0.034
489
AGN012 Agnathia-Otocephaly Complex 53 0.034
490
GLC077 Glucocorticoid Therapy, Response to 16 0.034
491
P ESS003 Essential Thrombocythemia 70 0.034
492
c SYS004 Systemic Mastocytosis 60 0.034
493
c BRT034 Bartter Syndrome, Type 2 46 0.034
494
XLN215 X-Linked Congenital Generalized Hypertrichosis 16 0.034
495
MRK001 Merkel Cell Carcinoma 52 0.034
496
FLL008 Folliculitis 46 0.034
497
c CHR531 Charcot-Marie-Tooth Disease, Type 2d 36 0.033
498
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.033
499
PLY039 Polymorphic Reticulosis 19 0.033
500
GLC037 Glucocorticoid Resistance 62 0.033
501
TST014 Testicular Cancer 53 0.033
502
PLM017 Pulmonary Alveolar Microlithiasis 46 0.033
503
P HRD004 Hereditary Breast Ovarian Cancer 57 0.033
504
CRH005 Crohn's Colitis 52 0.033
505
LPR001 Lepromatous Leprosy 50 0.033
506
PRT094 Protoporphyria, Erythropoietic, X-Linked 28 0.033
507
IND005 Indolent B Cell Lymphoma 23 0.033
508
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.033
509
P CNN004 Connective Tissue Cancer 40 0.033
510
P PSD003 Pseudohypoaldosteronism 44 0.032
511
P CRN108 Cranioectodermal Dysplasia 1 48 0.032
512
HST009 Histiocytoma 47 0.032
513
ASP007 Aspiration Pneumonia 47 0.032
514
ANR004 Anuria 45 0.032
515
INT071 Intestinal Perforation 42 0.032
516
SML008 Small Intestine Lymphoma 40 0.032
517
DSS022 Disseminated Peritoneal Leiomyomatosis 17 0.032
518
c HMN023 Human T-Cell Leukemia Virus Type 3 14 0.032
519
VGT001 Vogt-Koyanagi-Harada Disease 54 0.032
520
FML037 Female Breast Cancer 50 0.032
521
OST085 Osteosarcoma, Somatic 63 0.031
522
CCC002 Coccidiosis 51 0.031
523
CLN015 Colon Adenocarcinoma 50 0.031
524
GNG011 Gingival Disease 46 0.031
525
BNM005 Bone Marrow Necrosis 32 0.031
526
GRD001 Giardiasis 40 0.031
527
INT277 Intellectual Disability-Developmental Delay-Contractures Syndrome 21 0.031
528
MSC077 Muscle Eye Brain Disease 57 0.031
529
UTR033 Uterine Corpus Cancer 49 0.031
530
INF058 Inflammatory Myofibroblastic Tumor 47 0.031
531
c ART120 Arthrogryposis, Distal, Type 3 42 0.031
532
c FML108 Familial Breast Cancer 57 0.030
533
CRT002 Cartilage-Hair Hypoplasia 57 0.030
534
CRP002 Croup 37 0.030
535
c CNN010 Connective Tissue Benign Neoplasm 32 0.030
536
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 40 0.030
537
RNL021 Renal Tubular Transport Disease 32 0.030
538
P KRT005 Keratoacanthoma 46 0.030
539
THY043 Thymic Hyperplasia 32 0.030
540
P CMR001 Camurati-Engelmann Disease 58 0.030
541
c PRM038 Primary Agammaglobulinemia 30 0.030
542
IST006 Isotretinoin Syndrome 24 0.029
543
ICH002 Ichthyosis Bullosa of Siemens 45 0.029
544
FXF002 Fox-Fordyce Disease 36 0.029
545
SBC024 Subcutaneous Panniculitis-Like T-Cell Lymphoma 34 0.029
546
RNL101 Renal Cell Carcinoma, Papillary 63 0.029
547
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 40 0.029
548
CLL021 Collagenous Colitis 39 0.029
549
LNG013 Lung Lymphoma 38 0.029
550
EPD005 Epidural Abscess 33 0.029
551
PLY021 Polyradiculopathy 31 0.029
552
THY025 Thymus Cancer 50 0.028
553
c SPR009 Sporadic Breast Cancer 47 0.028
554
WRT002 Writing Disorder 27 0.028
555
OVR078 Ovarian Cancer, Somatic 50 0.028
556
ULC007 Ulcerative Stomatitis 44 0.028
557
CMB003 Combined T Cell and B Cell Immunodeficiency 42 0.028
558
LKP003 Leukoplakia 38 0.028
559
c THR110 Thrombocytopenia 6 20 0.028
560
GNG012 Gingival Overgrowth 52 0.028
561
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 0.028
562
DYS016 Dysgammaglobulinemia 37 0.028
563
KDN013 Kidney Hypertrophy 31 0.028
564
c LDD003 Liddle Syndrome, Scnn1b-Related 19 0.028
565
c LDD004 Liddle Syndrome, Scnn1g-Related 19 0.028
566
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 18 0.028
567
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 41 0.027
568
CLR012 Clear Cell Adenofibroma 33 0.027
569
IMM066 Immunodeficiency 9 30 0.027
570
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 27 0.027
571
ALD010 Aldosteronism, Glucocorticoid-Remediable 49 0.027
572
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 48 0.027
573
CRY001 Cryptogenic Organizing Pneumonia 44 0.027
574
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 44 0.027
575
OVR094 Ovarian Epithelial Cancer 43 0.027
576
P HVY001 Heavy Chain Disease 41 0.027
577
OPS001 Opisthorchiasis 36 0.027
578
HRT003 Heart Lymphoma 30 0.027
579
c LFR003 Li-Fraumeni Syndrome, Chek2-Related 20 0.027
580
VCC001 Vaccinia 46 0.026
581
IND002 Indolent Systemic Mastocytosis 41 0.026
582
IDP074 Idiopathic Bronchiectasis 36 0.026
583
GST014 Gastrointestinal Lymphoma 31 0.026
584
CBB005 Cobblestone Lissencephaly 27 0.026
585
c MSC124 Muscular Dystrophy, Congenital 55 0.026
586
CLN005 Colon Lymphoma 35 0.026
587
THY026 Thymus Gland Disease 27 0.026
588
ACR097 Acrodermatitis Chronica Atrophicans 27 0.026
589
PRM133 Primary Pulmonary Lymphoma 23 0.026
590
LYM009 Lymphocytic Choriomeningitis 43 0.025
591
SLT001 Solitary Osseous Plasmacytoma 36 0.025
592
LYM015 Lymphocytic Gastritis 31 0.025
593
IMM070 Immunodeficiency 13 27 0.025
594
c VRL006 Viral Esophagitis 26 0.025
595
BRC016 Brca1 and Brca2 Hereditary Breast and Ovarian Cancer 24 0.025
596
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.025
597
CNG101 Congenital Human Immunodeficiency Virus 19 0.025
598
STT009 Sutton Disease 2 18 0.025
599
UPP009 Upper Limb Hypertrophy 14 0.025
600
c PSD095 Pseudohypoaldosteronism, Type I 53 0.025
601
c GMM003 Gamma Heavy Chain Disease 46 0.025
602
c MSC050 Muscular Dystrophy, Congenital, 1b 37 0.025
603
CRN046 Corneal Fleck Dystrophy 36 0.025
604
HDG003 Hodgkin's Lymphoma, Lymphocytic Depletion 32 0.025
605
ORB009 Orbit Lymphoma 26 0.025
606
NCR009 Necrobiotic Xanthogranuloma 22 0.025
607
PTY006 Pityriasis Lichenoides Et Varioliformis Acuta 21 0.025
608
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 17 0.025
609
c RNL033 Renal Carcinoma, Familial 12 0.025
610
c MSC042 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 46 0.024
611
c MSC035 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 44 0.024
612
c PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 44 0.024
613
c PSD096 Pseudohypoaldosteronism Type I, Autosomal Dominant 42 0.024
614
c MSC103 Muscular Dystrophy-Dystroglycanopathy , Type C, 4 36 0.024
615
CHR068 Chronic Nk-Cell Lymphocytosis 33 0.024
616
CHR076 Choriocarcinoma of the Testis 31 0.024
617
ESN017 Eosinophilic Granuloma 30 0.024
618
P MSC002 Muscular Dystrophy-Dystroglycanopathy 28 0.024
619
SBC019 Subcutaneous Mycosis 28 0.024
620
PRP013 Paraphimosis 28 0.024
621
IMM038 Immunodeficiency, Common Variable, 1 27 0.024
622
ACQ016 Acquired Pure Red Cell Aplasia 25 0.024
623
c FKR001 Fkrp-Related Muscle Diseases 23 0.024
624
ANG024 Angiofollicular Lymph Hyperplasia 15 0.024
625
c MSC059 Muscular Dystrophy, Limb-Girdle, Type 2l 37 0.023
626
ORL019 Oral Hairy Leukoplakia 34 0.023
627
c GLB007 Glioblastoma 3 31 0.023
628
FLL042 Folliculotropic Mycosis Fungoides 27 0.023
629
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 26 0.023
630
SKN021 Skin Sarcoma 25 0.023
631
INF137 Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovasuclar Malformations 20 0.023
632
THY006 Thymus Lymphoma 18 0.023
633
CMP062 Complication After Organ Transplantation 11 0.023
634
SML024 Small Intestine Cancer, Childhood 10 0.023
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