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

2994 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
c MYL006 Myeloid Leukemia 72 6.853
2
P LKM002 Leukemia 79 6.649
3
c CHR065 Chronic Myeloid Leukemia 74 5.797
4
P ACT019 Acute Myeloid Leukemia 94 5.785
5
c ACT073 Acute Leukemia 62 5.448
6
P ACT074 Acute Lymphocytic Leukemia 77 4.847
7
P ACT020 Acute T Cell Leukemia 43 4.676
8
P ACT009 Acute Monocytic Leukemia 61 4.644
9
c CHR090 Chronic Lymphocytic Leukemia 63 4.468
10
MGK001 Megakaryocytic Leukemia 57 4.361
11
P JVN004 Juvenile Myelomonocytic Leukemia 62 4.029
12
ACT119 Acute Promyelocytic Leukemia 55 3.815
13
P BCL009 B-Cell Chronic Lymphocytic Leukemia 54 3.766
14
NTR003 Natural Killer Cell Leukemia 56 3.724
15
ACT095 Acute Biphenotypic Leukemia 47 3.683
16
c ADL017 Adult T-Cell Leukemia 53 3.579
17
c TCL004 T-Cell Leukemia 49 3.563
18
c ACT115 Acute Myeloid Leukemia, Adult 36 3.399
19
P LYM026 Lymphoblastic Leukemia 56 3.389
20
HRY003 Hairy Cell Leukemia 62 3.338
21
TCL002 T-Cell Large Granular Lymphocyte Leukemia 56 3.113
22
CHL061 Childhood Leukemia 52 2.983
23
ACT098 Acute Erythroid Leukemia 29 2.967
24
c ADL052 Adult Acute Lymphocytic Leukemia 49 2.934
25
c MNC007 Monocytic Leukemia 59 2.907
26
c SBC004 Subacute Myeloid Leukemia 20 2.847
27
c ACT117 Acute Myelomonocytic Leukemia 51 2.818
28
c CHR285 Chronic Myelomonocytic Leukemia 46 2.811
29
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 18 2.809
30
PRL017 Prolymphocytic Leukemia 47 2.720
31
P BCL005 B Cell Prolymphocytic Leukemia 35 2.685
32
P SYS004 Systemic Mastocytosis 70 2.664
33
P PRC048 Precursor B-Cell Acute Lymphoblastic Leukemia 44 2.641
34
CNT018 Central Nervous System Leukemia 41 2.607
35
LRG008 Large Granular Lymphocyte Leukemia 40 2.581
36
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 13 2.564
37
PLS016 Plasma Cell Leukemia 42 2.534
38
NNN018 Noonan-Like Syndrome Disorder with or Without Juvenile Myelomonocytic Leukemia 22 2.530
39
CHR286 Chronic Neutrophilic Leukemia 38 2.512
40
ACT103 Acute Lymphoblastic Leukemia, Childhood 37 2.446
41
c LKM005 Leukemia, T-Cell, Chronic 13 2.446
42
LYM067 Lymphoid Leukemia 45 2.374
43
c PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 39 2.364
44
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 15 2.349
45
SBL003 Subleukemic Leukemia 11 2.346
46
FML083 Familial Platelet Disorder with Associated Myeloid Malignancy 31 2.227
47
TST003 Testicular Leukemia 21 2.203
48
c CHR064 Chronic Monocytic Leukemia 22 2.194
49
INH015 Inherited Acute Myeloid Leukemia 18 2.192
50
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 35 2.191
51
c TCL005 T-Cell Prolymphocytic Leukemia 42 2.153
52
c LKM004 Leukemia, B-Cell, Chronic 17 2.137
53
ACT114 Acute Myeloblastic Leukemia Without Maturation 23 2.134
54
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 12 2.134
55
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 12 2.121
56
ACT113 Acute Myeloblastic Leukemia with Maturation 28 2.115
57
HCL001 Hcl-V 21 2.095
58
NLL001 Null-Cell Leukemia 13 2.091
59
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 10 2.082
60
P PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 11 2.073
61
MST002 Mast-Cell Leukemia 50 2.027
62
ACT140 Acute Undifferentiated Leukemia 28 1.971
63
ALK003 Aleukemic Leukemia Cutis 18 1.923
64
P ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 32 1.920
65
NNT007 Neonatal Leukemia 30 1.908
66
PRB001 Pre-B-Cell Acute Lymphoblastic Leukemia 33 1.890
67
P LFR001 Li-Fraumeni Syndrome 93 1.882
68
CRB138 Core Binding Factor Acute Myeloid Leukemia 40 1.882
69
ACT177 Acute Basophilic Leukemia 29 1.882
70
c SBC006 Subacute Leukemia 13 1.860
71
RFR002 Refractory Hairy Cell Leukemia 10 1.851
72
c SBC015 Subacute Monocytic Leukemia 11 1.842
73
LKM036 Leukemia, Acute Nonlymphocytic 11 1.832
74
ALK002 Aleukemic Monocytic Leukemia Cutis 9 1.832
75
ACT097 Acute Erythroblastic Leukemia 7 1.829
76
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 11 1.821
77
PLS003 Plasmacytic Leukemia 11 1.813
78
BLN016 Bilineal Acute Leukemia 10 1.803
79
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 7 1.798
80
PDT026 Pediatric T-Cell Leukemia 2 1.798
81
ALK014 Aleukemic Mast Cell Leukemia 8 1.711
82
c ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 18 1.706
83
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 19 1.689
84
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 33 1.615
85
c 8P1002 8p11 Myeloproliferative Syndrome 27 1.564
86
c FML114 Familial Chronic Lymphocytic Leukemia 27 1.560
87
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 30 1.557
88
P LKM024 Leukemia/lymphoma, T-Cell 25 1.550
89
c HMN022 Human T-Cell Leukemia Virus Type 2 29 1.537
90
c HMN021 Human T-Cell Leukemia Virus Type 1 27 1.529
91
CLL014 Cll/sll 26 1.529
92
ACT118 Acute Non Lymphoblastic Leukemia 20 1.519
93
c ACT106 Acute Myeloblastic Leukemia Type 1 5 1.516
94
c ACT107 Acute Myeloblastic Leukemia Type 2 5 1.513
95
P ACT108 Acute Myeloblastic Leukemia Type 3 5 1.509
96
c ACT110 Acute Myeloblastic Leukemia Type 5 5 1.502
97
c ACT111 Acute Myeloblastic Leukemia Type 6 5 1.498
98
HRY001 Hairy Cell Leukemia of Spleen 13 1.493
99
c ACT112 Acute Myeloblastic Leukemia Type 7 5 1.493
100
c PRC017 Precursor Lymphoblastic Lymphoma/leukemia 9 1.489
101
c ACT109 Acute Myeloblastic Leukemia Type 4 4 1.489
102
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 11 1.484
103
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 7 1.484
104
ACT178 Acute Myeloid Leukemia with Multilineage Dysplasia 12 1.478
105
SPL013 Splenic Manifestation of Leukemia 8 1.478
106
c HMN023 Human T-Cell Leukemia Virus Type 3 4 1.478
107
c FML095 Familial Acute Lymphocytic Leukemia 4 1.472
108
c MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 2 1.472
109
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 8 1.466
110
TCL013 T-Cell Prolymphocytic Leukemia, Somatic 6 1.466
111
P FML115 Familial Chronic Myelocytic Leukemia 3 1.466
112
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 1 1.466
113
ACT116 Acute Myeloid Leukemia, Childhood 1 1.466
114
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 12 1.458
115
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 9 1.458
116
LKM016 Leukemia, Acute Myeloid, Somatic 9 1.458
117
LKM017 Leukemia, Acute Myeloid, Reduced Survival in 9 1.458
118
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 8 1.458
119
MYL050 Myeloid Leukemia, Acute, M4/m4eo Subtype, Somatic 8 1.458
120
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 7 1.458
121
c LKM009 Leukemia/lymphoma, B-Cell, 2 6 1.458
122
c LKM010 Leukemia/lymphoma, B-Cell, 3 6 1.458
123
LKM018 Leukemia, T-Cell Acute Lymphoblastoid 6 1.458
124
LKM026 Leukemia, Acute Myeloid, Therapy-Related 6 1.458
125
LKM058 Leukemia, Acute Lymphoblastic, Somatic 6 1.458
126
c LYM061 Lymphocytic Leukemia, Acute T-Cell 6 1.458
127
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 5 1.458
128
LKM008 Leukemia, Acute Pre-B-Cell 5 1.458
129
LKM020 Leukemia, Acute Myeloid, with Eosinophilia 5 1.458
130
LKM023 Leukemia, Myeloid/lymphoid or Mixed-Lineage 5 1.458
131
BND002 B- and T-Cell Mixed Leukemia 5 1.458
132
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 4 1.458
133
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 4 1.458
134
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 4 1.458
135
CLS019 Classic Mast Cell Leukemia 4 1.458
136
LKM019 Leukemia, Philadelphia Chromosome-Positive, Resistant to Imatinib 4 1.458
137
LKM022 Leukemia, Acute Promyelocytic, Pml/rara Type 4 1.458
138
LKM035 Leukemia, Acute Promyelocytic, Stat5b/rara Type 4 1.458
139
LKM037 Leukemia, Acute Promyelocytic, Numa/rara Type 4 1.458
140
LKM038 Leukemia, Acute Promyelocytic, Npm/rara Type 4 1.458
141
LKM039 Leukemia, Acute Promyelocytic, Pl2f/rara Type 4 1.458
142
c LKM050 Leukemia, Chronic Lymphocytic 1 4 1.458
143
c LKM051 Leukemia, Chronic Lymphocytic 3 4 1.458
144
c LKM052 Leukemia, Chronic Lymphocytic 5 4 1.458
145
c LKM053 Leukemia, Chronic Lymphocytic 4 4 1.458
146
c LKM054 Leukemia, Acute Lymphocytic 1 4 1.458
147
c LKM055 Leukemia, Acute Lymphoblastic 2 4 1.458
148
c LKM056 Leukemia, Chronic Lymphocytic 2 4 1.458
149
LKM057 Leukemia, Post-Chemotherapy 4 1.458
150
c LYM062 Lymphoma/leukemia, B-Cell, Variant 4 1.458
151
c NPM001 Npm1-Related Acute Myeloid Leukemia 4 1.458
152
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 4 1.458
153
LKM034 Leukemia, Transient, of Down Syndrome 3 1.458
154
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 3 1.458
155
SPL010 Splenic Manifestation of Hairy Cell Leukemia 3 1.458
156
c FML096 Familial Acute Myelocytic Leukemia 2 1.458
157
EMB016 Emberger Syndrome 26 1.205
158
LYM040 Lymphoblastic Lymphoma 42 1.178
159
ACT187 Activated Pi3k-Delta Syndrome 13 1.166
160
P FML045 Familial Mosaic Monosomy 7 Syndrome 13 1.136
161
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 1.131
162
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 18 1.109
163
DGG001 Di Guglielmo's Syndrome 4 1.106
164
P HYP098 Hypereosinophilic Syndrome 54 1.100
165
ACT188 Activated Pi3k-Delta Immunodeficiency Syndrome 13 1.096
166
CRB137 Cerebral Creatine Deficiency Syndrome 24 1.085
167
NSY001 N Syndrome 55 1.049
168
WTL001 Wt Limb Blood Syndrome 23 1.031
169
c XP2001 Xp22.3 Microdeletion Syndrome 21 0.358
170
SCD002 Scid, Autosomal Recessive, T-Negative/b-Positive Type 23 0.297
171
END072 Endotheliitis 47 0.289
172
FMR002 Femoral Cancer 25 0.272
173
END017 Endocardium Cancer 18 0.258
174
P ADL001 Adult Lymphoma 24 0.248
175
MND001 Mandibular Cancer 31 0.225
176
SVR047 Severe Combined Immunodeficiency Due to Dna-Pkcs Deficiency 19 0.225
177
GRF006 Grfoma 26 0.220
178
c SNS011 Sinus Cancer 23 0.211
179
IDP042 Idiopathic Recurrent Stupor 15 0.205
180
DWN001 Down Syndrome 62 0.198
181
ANK002 Ankylosing Spondylitis 75 0.197
182
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 30 0.195
183
SPR021 Supraglottis Cancer 22 0.193
184
NNN017 Noonan/ Costello/ Leopard/ Cardiofaciocutaneous Syndrome Multi-Gene Panels 13 0.191
185
LYM019 Lymphosarcoma 54 0.188
186
SCN006 Secondary Syphilis 55 0.188
187
SVR036 Severe Combined Immune Deficiency, Autosomal Recessive T Cell-Negative, B Cell-Positive, Nk Cell-Positive, Il7r-Related 17 0.188
188
THR013 Thoracic Outlet Syndrome 54 0.187
189
P LNG032 Lung Cancer 74 0.185
190
BLS007 Blastic Plasmacytoid Dendritic Cell 29 0.169
191
DST056 Distal 22q11.2 Microdeletion Syndrome 37 0.169
192
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 28 0.167
193
IMM068 Immunodeficiency 8 28 0.167
194
14Q004 14q22q23 Microdeletion Syndrome 29 0.166
195
MLN020 Melanoma, Malignant, Somatic 51 0.164
196
3Q2005 3q26q27 Microdeletion Syndrome 14 0.164
197
ERL004 Early Yaws 33 0.161
198
P ATX002 Ataxia Telangiectasia 93 0.160
199
c LNG057 Long Qt Syndrome 13 19 0.158
200
c MYL007 Myeloma 59 0.156
201
SVR020 Severe Combined Immune Deficiency Multi-Gene Panels 12 0.156
202
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 44 0.155
203
c CLL013 Cell Type Cancer 50 0.150
204
P PNC035 Pancreatic Cancer 95 0.150
205
c CNG124 Congenital Rubella 42 0.148
206
SRC014 Sarcoma 63 0.147
207
P SRC025 Sarcoidosis 1 32 0.146
208
SPS077 Sepsis 58 0.144
209
CNJ009 Conjunctival Cancer 21 0.143
210
PRL042 Proliferating Trichilemmal Cyst 38 0.140
211
MYL003 Myeloid Sarcoma 54 0.139
212
VLL005 Vallecula Cancer 20 0.139
213
MLD010 Mild Phenylketonuria 14 0.139
214
FTL044 Fetal Cytomegalovirus Syndrome 28 0.138
215
TFT003 Tufting Enteropathy 21 0.138
216
c TCL008 T-Cell Lymphoma 1a 12 0.138
217
LKS001 Leukostasis 48 0.135
218
P BRS047 Breast Cancer 105 0.134
219
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 44 0.132
220
P MLT019 Multiple Myeloma 89 0.131
221
MYC006 Mycosis Fungoides 71 0.128
222
CLC008 Colchicine Resistance 26 0.127
223
P GRF002 Graft Versus Host Disease 65 0.126
224
GLL008 Gilles De La Tourette Syndrome 73 0.124
225
BRN024 Bronchitis 76 0.123
226
ADS010 Aids, Slow Progression to 26 0.123
227
c XQ1001 Xq12-Q13.3 Duplication Syndrome 11 0.123
228
JBR008 Juberg-Hayward Syndrome 21 0.122
229
P SPR035 Superior Vena Cava Syndrome 19 0.122
230
RHB001 Rhabdoid Cancer 38 0.122
231
UVL001 Uvula Cancer 19 0.122
232
CRB132 Cerebral Sinovenous Thrombosis 32 0.121
233
PRR002 Pure Red-Cell Aplasia 54 0.120
234
DNT005 Dentatorubral-Pallidoluysian Atrophy 61 0.119
235
ORB012 Orbital Cancer 31 0.119
236
NNS006 Non-Suppurative Otitis Media 26 0.119
237
P MYL005 Myelofibrosis 75 0.118
238
SPS019 Spastic Paraparesis 35 0.118
239
TLY002 T-Lymphocytopenia 34 0.118
240
STR017 Sternum Cancer 23 0.118
241
WST005 West Nile Virus 35 0.117
242
PRP010 Prepuce Cancer 18 0.116
243
HDG007 Hodgkin's Lymphoma 91 0.116
244
P FNC001 Fanconi's Anemia 67 0.116
245
P AVS004 Avascular Necrosis of the Femoral Head 49 0.116
246
c NTR004 Neutropenia 65 0.115
247
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 43 0.115
248
SFT003 Soft Tissue Sarcoma 32 0.115
249
BNZ002 Benzene Toxicity 26 0.115
250
SPR094 Sporadic Pheochromocytoma 32 0.113
251
ICH002 Ichthyosis Bullosa of Siemens 50 0.112
252
MLT034 Multicystic Renal Dysplasia, Bilateral 25 0.112
253
c ATM010 Autoimmune Hemolytic Anemia 57 0.112
254
P PRS040 Prostate Cancer 91 0.111
255
LNG024 Langerhans-Cell Histiocytosis 75 0.110
256
c LCL006 Localized Scleroderma 68 0.110
257
BRN056 Bronchopulmonary Dysplasia 47 0.110
258
LJN002 Lujan Syndrome 36 0.110
259
c RFR011 Refractory Anemia with Excess Blasts-2 13 0.110
260
c HPT021 Hepatitis 75 0.109
261
14Q001 14q12 Microdeletion Syndrome 23 0.109
262
c RNG028 Ring Chromosome Y 14 0.109
263
P DFF005 Diffuse Large B-Cell Lymphoma 63 0.108
264
SPN119 Spondylarthropathy 35 0.107
265
FCT013 Factor V Leiden Thrombophilia 35 0.107
266
MLT075 Multifocal Motor Neuropathy 34 0.107
267
WDM003 Wiedemann Opitz Syndrome 8 0.107
268
ACN002 Acanthosis Nigricans 73 0.106
269
P ESN007 Eosinophilia 60 0.106
270
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 45 0.105
271
FML055 Familial Cylindromatosis 39 0.105
272
THR035 Thrombasthenia 37 0.105
273
PRN029 Parainfluenza Virus Type 3 33 0.105
274
MNS013 Monosomy 13q34 17 0.105
275
c DST058 Distal Monosomy 12p 17 0.105
276
P NRF002 Neurofibromatosis 100 0.104
277
ALL014 Allergic Encephalomyelitis 34 0.104
278
THR004 Thrombocytosis 63 0.102
279
ENT015 Enthesitis-Related Arthritis 48 0.102
280
CHL079 Children's Interstitial Lung Disease 46 0.102
281
TRP002 Tropical Spastic Paraparesis 67 0.101
282
DSM004 Desmoid Tumor 58 0.101
283
MCR071 Microdeletion 15q11.2 25 0.101
284
HYP179 Hypertrichosis Congenital Generalized X-Linked 24 0.101
285
HYP004 Hypercalcemia 69 0.100
286
c MST009 Mastocytosis 59 0.100
287
RTC002 Reticular Dysgenesis 58 0.100
288
SYN053 Syndromic Diarrhea 42 0.100
289
SVR031 Severe Combined Immunodeficiency, Athabascan Type 25 0.100
290
HNM002 Hinman Syndrome 24 0.100
291
SVR011 Severe Combined Immunodeficiency, Atypical 14 0.100
292
HYP439 Hyperammonemia Multi-Gene Panels 10 0.100
293
P HML002 Hemolytic Anemia 68 0.100
294
P UVT001 Uveitis 67 0.100
295
CRB009 Cerebritis 56 0.100
296
PST046 Post-Transplant Lymphoproliferative Disease 49 0.100
297
CYT008 Cytomegalovirus Infection 34 0.100
298
NNH001 Non-Hodgkin Lymphoma 72 0.099
299
WST001 West Syndrome 64 0.099
300
c ESS003 Essential Thrombocythemia 50 0.098
301
P SDR003 Sideroblastic Anemia 48 0.098
302
P HST010 Histiocytosis 71 0.097
303
17Q002 17q23.1q23.2 Microdeletion Syndrome 34 0.097
304
CRK001 Cork-Handlers' Disease 32 0.097
305
c FNC043 Fanconi Anemia, Complementation Group E 24 0.097
306
P CHR092 Chronic Myeloproliferative Disease 55 0.096
307
HPT023 Hepatocellular Carcinoma 89 0.096
308
SDR002 Siderosis 53 0.096
309
P IDP049 Idiopathic Anterior Uveitis 30 0.096
310
HMT002 Hematologic Cancer 64 0.095
311
RFR010 Refractory Anemia 39 0.095
312
c LNG056 Long Qt Syndrome 12 20 0.095
313
BRL003 Bare Lymphocyte Syndrome 27 0.094
314
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 13 0.094
315
BRK003 Burkitt's Lymphoma 78 0.093
316
LKM001 Leukemoid Reaction 45 0.093
317
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 32 0.093
318
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 31 0.093
319
17Q007 17q11 Microdeletion Syndrome 26 0.093
320
c 2Q3005 2q31.1 Microdeletion Syndrome 26 0.093
321
SVR042 Severe Combined Immunodeficiency Due to Lck Deficiency 19 0.093
322
RBR001 Roberts Syndrome 62 0.092
323
MXL004 Maxillary Sinus Squamous Cell Carcinoma 43 0.092
324
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 43 0.092
325
ACQ031 Acquired Idiopathic Sideroblastic Anemia 24 0.092
326
c RCR005 Recurrent Fever Multi-Gene Panels 11 0.092
327
P NJM001 Nijmegen Breakage Syndrome 74 0.091
328
c MLG054 Malignant Histiocytosis 60 0.091
329
MDS022 Mediastinitis 56 0.091
330
P HMP002 Hemophagocytic Lymphohistiocytosis 66 0.091
331
c ACR001 Aicardi-Goutieres Syndrome 49 0.091
332
RCH001 Richter's Syndrome 48 0.091
333
CRY021 Cryoglobulinemic Vasculitis 41 0.091
334
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 35 0.091
335
PRT015 Partial Third-Nerve Palsy 26 0.091
336
P ATX025 Ataxia, Spastic, 5, Autosomal Recessive 20 0.091
337
c FML139 Familial Myeloma 18 0.091
338
XP2002 Xp22.13p22.2 Duplication Syndrome 15 0.091
339
DMD001 Demodicidosis 13 0.091
340
INT229 Intellectual Disability-Brachydactyly-Pierre Robin Syndrome 13 0.091
341
ENT001 Enterocele 42 0.090
342
EMN001 Emanuel Syndrome 36 0.090
343
CRV045 Cervical Intraepithelial Neoplasia 36 0.090
344
PRX070 Proximal 16p11.2 Microduplication Syndrome 18 0.090
345
c TTL001 Total Internal Ophthalmoplegia 17 0.090
346
PLY039 Polymorphic Reticulosis 16 0.090
347
P CRV035 Cervical Cancer 62 0.089
348
PLY041 Polymyositis 54 0.089
349
c PRM046 Primary Malignant Lymphoma 31 0.089
350
BRG002 Berger Disease 27 0.089
351
ESP021 Esophageal Cancer 81 0.088
352
P ANG001 Angelman Syndrome 70 0.088
353
ART019 Aortic Valve Stenosis 68 0.088
354
PRS047 Prostatitis 62 0.088
355
P THR012 Thoracic Cancer 56 0.088
356
EGG001 Egg Allergy 54 0.088
357
RPP001 Rapp-Hodgkin Syndrome 34 0.088
358
c BNG076 Benign Exophthalmos Syndrome 21 0.088
359
P HMP004 Hemophilia B 80 0.087
360
P THY023 Thymoma 66 0.087
361
HYD012 Hydrops Fetalis 53 0.087
362
INV001 Invasive Aspergillosis 49 0.087
363
VNS010 Venous Thromboembolism 42 0.087
364
TBR011 Tuberculous Meningitis 40 0.087
365
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.087
366
OCL020 Ocular Cicatricial Pemphigoid 37 0.087
367
DSC009 Discoid Lupus Erythematosus 34 0.087
368
ZP7001 Zap70-Related Severe Combined Immunodeficiency 33 0.087
369
GLM037 Glioma Somatic 31 0.087
370
P SLP004 Salpingo-Oophoritis 31 0.087
371
c CHR243 Chromosome 3p Deletion 23 0.087
372
SVR022 Severe Combined Immune Deficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive, Rag1/rag2-Related 17 0.087
373
P APL001 Aplastic Anemia 83 0.086
374
P ART022 Arthritis 75 0.086
375
c MNN013 Meningitis 71 0.086
376
PRP030 Purpura 67 0.086
377
c LRY016 Laryngeal Carcinoma 63 0.086
378
EMB003 Embryonal Cancer 55 0.086
379
BRN016 Bronchogenic Carcinoma 55 0.086
380
SPN040 Spinal Cancer 40 0.086
381
BRC055 Brca2 Hereditary Breast and Ovarian Cancer 37 0.086
382
PYL007 Pylorus Cancer 25 0.086
383
CRN021 Cornea Cancer 22 0.086
384
CHR410 Choroid Cancer 20 0.086
385
EPC001 Epicardium Cancer 18 0.086
386
BRC054 Brca1 Hereditary Breast and Ovarian Cancer 16 0.086
387
IST001 Isthmus Cancer 16 0.086
388
SVR004 Severe Combined Immunodeficiency 85 0.085
389
P THR090 Thrombocythemia 1 54 0.085
390
P RSP003 Respiratory Failure 70 0.084
391
RLP001 Relapsing Polychondritis 69 0.084
392
DSS009 Disseminated Intravascular Coagulation 66 0.084
393
IRN001 Iron Deficiency Anemia 61 0.084
394
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 36 0.084
395
PNS012 Paine Syndrome 35 0.084
396
P INF069 Infantile Neuroaxonal Dystrophy 1 32 0.084
397
LYL001 Lyell Syndrome 32 0.084
398
19Q001 19q13.11 Microdeletion Syndrome 25 0.084
399
c CHR224 Chromosome 1q Duplication 19 0.084
400
MYC003 Myocardium Cancer 18 0.084
401
c THR014 Thrombocytopenia 67 0.083
402
MLR002 Miliary Tuberculosis 55 0.083
403
P DNS004 Duane Syndrome Type 2 41 0.083
404
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.083
405
CRT001 Carotid Body Cancer 20 0.083
406
c DYS055 Dystonia 10 19 0.083
407
P RHM011 Rheumatoid Arthritis 91 0.081
408
PLY001 Polycythemia Vera 83 0.081
409
P PNM007 Pneumonia 79 0.081
410
c PRP029 Porphyria 64 0.081
411
c PLY018 Polycythemia 61 0.081
412
APH001 Aphthous Stomatitis 59 0.081
413
EVN001 Evans' Syndrome 54 0.081
414
P END033 Endocarditis 48 0.081
415
PYM001 Pyomyositis 47 0.081
416
P CRT033 Corticobasal Degeneration 45 0.081
417
MCS003 Mucous Membrane Pemphigoid 44 0.081
418
P ADM005 Adams-Oliver Syndrome 1 36 0.081
419
LKP003 Leukoplakia 32 0.081
420
P XQ2001 Xq27.3q28 Duplication Syndrome 27 0.081
421
P MLR006 Male Reproductive Organ Cancer 23 0.081
422
WDM004 Wiedemann-Steiner Syndrome 22 0.081
423
GNR028 Generalized Essential Telangiectasia 16 0.081
424
TRS012 Trisomy 22 13 0.081
425
ASP006 Aspergillosis 73 0.080
426
VSC011 Vasculitis 67 0.080
427
P DBT005 Diabetes Insipidus 57 0.080
428
EXT010 Extramedullary Plasmacytoma 55 0.080
429
SYN008 Synovium Cancer 20 0.080
430
P MLN008 Melanoma 65 0.079
431
PLM019 Pleomorphic Liposarcoma 45 0.079
432
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 45 0.079
433
VND002 Van Der Woude Syndrome 43 0.079
434
DDF001 Dedifferentiated Liposarcoma 42 0.079
435
TRP014 Triploidy 41 0.079
436
PCH007 Pouchitis 40 0.079
437
CHR020 Chronic Interstitial Cystitis 38 0.079
438
c 3Q2003 3q29 Microdeletion Syndrome 36 0.079
439
P FLL037 Follicular Lymphoma 36 0.079
440
BLD087 Bladder Cancer, Somatic 34 0.079
441
LYM045 Lymphocytic Vasculitis 34 0.079
442
NRG004 Neurogenic Diabetes Insipidus 34 0.079
443
ZYG002 Zygomycosis 28 0.079
444
ACT167 Acute Generalized Exanthematous Pustulosis 25 0.079
445
VRS001 Virus Associated Hemophagocytic Syndrome 24 0.079
446
ZP7002 Zap-70 Deficiency 22 0.079
447
AND002 Androgen Insensitivity Syndrome 88 0.078
448
MNT001 Mantle Cell Lymphoma 67 0.078
449
c AXN002 Axenfeld-Rieger Syndrome 60 0.078
450
MCR004 Macroglobulinemia 55 0.078
451
P HYP117 Hypertriglyceridemia 54 0.078
452
PRP016 Paraplegia 48 0.078
453
EPT020 Epithelioid Hemangioendothelioma 44 0.078
454
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.078
455
STR077 Streptococcal Toxic-Shock Syndrome 34 0.078
456
HMC004 Homocysteine Plasma Level 27 0.078
457
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 24 0.078
458
P ALZ001 Alzheimer's Disease 103 0.077
459
ABT001 Abetalipoproteinemia 73 0.077
460
IPX001 Ipex Syndrome 39 0.077
461
ANG049 Angioedema Induced by Ace Inhibitors 31 0.077
462
MYC002 Mycobacterium Avium Complex Disease 57 0.076
463
VTM002 Vitamin B12 Deficiency 51 0.076
464
LRN002 Laron Syndrome 76 0.075
465
GMM002 Gamma Chain Deficiency 66 0.075
466
MLT022 Malt Lymphoma 48 0.075
467
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 43 0.075
468
MMR004 Memory Impairment 41 0.075
469
c CHR417 Chronic Graft Versus Host Disease 40 0.075
470
c MYL014 Myeloproliferative Disorder 39 0.075
471
GRW007 Growth Hormone Deficiency 39 0.075
472
PRG060 Pregnancy Loss 38 0.075
473
P RNG004 Ring Chromosome 1 29 0.075
474
CNT060 Central Serous Chorioretinopathy 28 0.075
475
c PRM041 Primary Cortisol Resistance 13 0.075
476
CYT018 Cytochrome P450 2d6 Variant 13 0.075
477
P ALP006 Alpha Thalassemia 75 0.074
478
P INF038 Influenza 69 0.074
479
c THY032 Thyroiditis 67 0.074
480
ACQ007 Acquired Immunodeficiency Syndrome 63 0.074
481
RTN023 Retinitis 61 0.074
482
CNG008 Congenital Ichthyosiform Erythroderma 53 0.074
483
c FML024 Familial Melanoma 51 0.074
484
c KBK001 Kabuki Syndrome 48 0.074
485
P ATX010 Ataxia Neuropathy Spectrum 44 0.074
486
JVN033 Juvenile Nasopharyngeal Angiofibroma 39 0.074
487
STN007 Stenotrophomonas Maltophilia 35 0.074
488
17Q004 17q12 Microdeletion Syndrome 33 0.074
489
BCK006 Back Pain 33 0.074
490
DND015 Dendritic Cell, Monocyte, B Lymphocyte, and Natural Killer Lymphocyte Deficiency 24 0.074
491
P PNC001 Pancytopenia 55 0.073
492
c NNN003 Noonan Syndrome 77 0.072
493
P SVR003 Severe Congenital Neutropenia 59 0.072
494
PRN001 Purine Nucleoside Phosphorylase Deficiency 55 0.072
495
TLN003 Telangiectasis 46 0.072
496
UTR043 Uterine Sarcoma 41 0.072
497
URT008 Urticaria Pigmentosa 40 0.072
498
c ATX004 Ataxia 38 0.072
499
HMN016 Hemangioendothelioma 38 0.072
500
RHB022 Rhabdoid Tumors, Somatic 34 0.072
501
P BNL002 Bone Lymphoma 33 0.072
502
12P001 12p12.1 Microdeletion Syndrome 16 0.072
503
c BSL011 Basal Cell Carcinoma, Multiple 15 0.072
504
P RTN024 Retinoblastoma 86 0.071
505
NRP001 Neuropathy 61 0.071
506
APP008 Appendicitis 57 0.071
507
P CRV039 Cervicitis 52 0.071
508
GRY002 Gray Platelet Syndrome 51 0.071
509
P PND001 Pain Disorder 49 0.071
510
P INS005 Insulin Resistance 48 0.071
511
XLN005 X-Linked Hyper Igm Syndrome 45 0.071
512
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.071
513
c BRN111 Bernard-Soulier Syndrome, Type A2 30 0.071
514
SVR038 Severe Combined Immune Deficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive, Cd3d-Related 17 0.071
515
GNR023 Generalized Eruptive Histiocytosis 15 0.071
516
INT206 Intellectual Deficit, X-Linked - Macrocephaly - Macro-Orchidism 13 0.071
517
MTH028 Mthfr Thermolabile Variant 13 0.071
518
MYL040 Myelodysplastic Syndromes 64 0.070
519
DPH001 Diphtheria 59 0.070
520
SRS001 Serous Cystadenocarcinoma 57 0.070
521
P ALV004 Alveolar Rhabdomyosarcoma 51 0.070
522
CRY001 Cryptogenic Organizing Pneumonia 44 0.070
523
P CTN015 Cutaneous T Cell Lymphoma 44 0.070
524
URC001 Urachus Cancer 18 0.070
525
P RTT002 Rett Syndrome 85 0.069
526
c LPR002 Leopard Syndrome 72 0.069
527
P GLM007 Glomerulonephritis 66 0.069
528
P CND004 Candidiasis 63 0.069
529
DBL002 Double Outlet Right Ventricle 57 0.069
530
c PST005 Posterior Uveitis 53 0.069
531
c XRD012 Xeroderma Pigmentosum, Group D 51 0.069
532
SPT013 Septic Shock 48 0.069
533
1P3001 1p36 Deletion Syndrome 48 0.069
534
c CPL003 Capillary Leak Syndrome 47 0.069
535
c ALM001 Al Amyloidosis 44 0.069
536
SPR005 Superficial Basal Cell Carcinoma 43 0.069
537
GNT031 Genitopatellar Syndrome 42 0.069
538
CMB021 Combined Pituitary Hormone Deficiency 40 0.069
539
OLG006 Oligoastrocytoma 39 0.069
540
MLN045 Melanoma of Soft Part 36 0.069
541
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 36 0.069
542
c RFR008 Refractory Anemia with Excess Blasts 32 0.069
543
ABL001 Ablepharon Macrostomia Syndrome 29 0.069
544
BLT011 Bilateral Perisylvian Polymicrogyria 27 0.069
545
MLG083 Male Germ Cell Tumor 24 0.069
546
MYC018 Mycobacterium Malmoense 24 0.069
547
CHL109 Childhood Apraxia of Speech 24 0.069
548
DST051 Distal 7q11.23 Microdeletion Syndrome 21 0.069
549
HRD009 Hereditary Wilms' Tumor 21 0.069
550
LKN016 Leukoencephalopathy with Mild Cerebellar Ataxia and White Matter Edema 21 0.069
551
12Q001 12q15q21.1 Microdeletion Syndrome 15 0.069
552
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 14 0.069
553
c CHR245 Chromosome 3q Deletion 12 0.069
554
STR008 Strongyloidiasis 61 0.068
555
PYD001 Pyoderma Gangrenosum 57 0.068
556
ECT003 Ectopic Thymus 21 0.068
557
P ADL010 Adult Respiratory Distress Syndrome 71 0.066
558
c ACT134 Acute Liver Failure 57 0.066
559
ADL002 Adult Syndrome 52 0.066
560
P JBR004 Joubert Syndrome 2 52 0.066
561
MNN014 Mononeuritis 48 0.066
562
NRP002 Neuroepithelioma 41 0.066
563
PNM013 Pneumococcal Meningitis 39 0.066
564
ATP002 Atopy 38 0.066
565
ADS004 Aids Dementia Complex 38 0.066
566
ICH020 Ichthyosis Prematurity Syndrome 38 0.066
567
ANP009 Anaplastic Oligodendroglioma 38 0.066
568
MSC006 Muscle Glycogenosis 36 0.066
569
THP001 Thiopurine S Methyltranferase Deficiency 29 0.066
570
IMM062 Immunodeficiency 11 28 0.066
571
RHB020 Rhabdomyosarcoma, Somatic 27 0.066
572
HYP084 Hypopyon 27 0.066
573
LYM032 Lymphoplasmacytoid Lymphoma 14 0.066
574
MTR030 Mitral Valve Prolapse, Familial, X-Linked 12 0.066
575
P NRB001 Neuroblastoma 71 0.065
576
c CWD001 Cowden Disease 69 0.065
577
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.065
578
ART001 Arterial Tortuosity Syndrome 62 0.065
579
PRG009 Progressive Multifocal Leukoencephalopathy 57 0.065
580
HYP063 Hypersplenism 56 0.065
581
HPT032 Hepatocellular Carcinoma, Somatic 50 0.065
582
NPH018 Nephrogenic Systemic Fibrosis 44 0.065
583
AND003 Andersen-Tawil Syndrome 43 0.065
584
CHR055 Chordoid Meningioma 42 0.065
585
INT038 Interdigitating Dendritic Cell Sarcoma 39 0.065
586
PRP034 Purpura Fulminans 38 0.065
587
SPL018 Splenomegaly 37 0.065
588
LYM105 Lymphoma, Follicular, Somatic 36 0.065
589
c CHR253 Chromosome 5q Deletion 28 0.065
590
c MNS010 Monosomy Xp21 20 0.065
591
c MNS014 Monosomy 22 12 0.065
592
GNG013 Gingivitis 67 0.064
593
c HPT016 Hepatitis B 65 0.064
594
PRT011 Protein C Deficiency 60 0.064
595
CHL056 Cheilitis 54 0.064
596
CRS001 Crescentic Glomerulonephritis 51 0.064
597
P WLD002 Waldenstrom Macroglobulinemia 44 0.064
598
c RSM001 Rasmussen Encephalitis 37 0.064
599
HST016 Histiocytic Sarcoma 36 0.064
600
MYL046 Myelodysplastic Syndrome, Somatic 36 0.064
601
SPL009 Splenic Sequestration 25 0.064
602
SCD001 Scid Due to Lck Deficiency 15 0.064
603
P ADN016 Adenocarcinoma 60 0.063
604
OCC006 Occipital Horn Syndrome 57 0.063
605
DBT004 Diabetic Polyneuropathy 57 0.063
606
DSM007 Desmoplastic Small Round Cell Tumor 48 0.063
607
LMB024 Limbic Encephalitis 37 0.063
608
FLL019 Follicular Mucinosis 34 0.063
609
MSM004 Mesomelia-Synostoses Syndrome 32 0.063
610
CHR276 Chronic Active Epstein-Barr Virus Infection 32 0.063
611
12Q002 12q14 Microdeletion Syndrome 31 0.063
612
c CHR208 Chromosome 17p Deletion 29 0.063
613
5FL001 5-Fluorouracil Toxicity 28 0.063
614
c ANT034 Anterior Uveitis 28 0.063
615
2Q3003 2q32q33 Microdeletion Syndrome 27 0.063
616
c 2Q2001 2q23.1 Microdeletion Syndrome 27 0.063
617
c 4Q2001 4q21 Microdeletion Syndrome 23 0.063
618
SDD005 Sudden Cardiac Death Multi-Gene Panels 21 0.063
619
c CHR260 Chromosome 7p Deletion 15 0.063
620
c CHR255 Chromosome 6p Deletion 13 0.063
621
P PRP003 Porphyria Cutanea Tarda 81 0.062
622
P TRC032 Turcot Syndrome 70 0.062
623
P NRL016 Neural Tube Defects 67 0.062
624
CHR066 Chronic Fatigue Syndrome 65 0.062
625
P XRD018 Xeroderma Pigmentosum, Group a 61 0.062
626
c CNT035 Central Nervous System Disease 60 0.062
627
INT054 Intraocular Lymphoma 58 0.062
628
ADN011 Adenoid Cystic Carcinoma 58 0.062
629
HMG002 Hemoglobinuria 55 0.062
630
NCR004 Nocardiosis 54 0.062
631
RHB003 Rhabdomyosarcoma 54 0.062
632
DRM004 Dermatofibrosarcoma 53 0.062
633
HRD004 Hereditary Breast Ovarian Cancer 50 0.062
634
RHY001 Rhyns Syndrome 49 0.062
635
PDT021 Pediatric Osteosarcoma 48 0.062
636
PRS008 Prostate Small Cell Carcinoma 47 0.062
637
HPR003 Heparin-Induced Thrombocytopenia 45 0.062
638
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 40 0.062
639
ANG046 Angioimmunoblastic T-Cell Lymphoma 37 0.062
640
P AGM005 Agammaglobulinemia, X-Linked 1 36 0.062
641
INT103 Intrauterine Infections 36 0.062
642
P EWN002 Ewing's Family of Tumors 36 0.062
643
P HYD008 Hydrocephalus Due to Aqueductal Stenosis 35 0.062
644
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 32 0.062
645
LPT005 Leptin Deficiency 30 0.062
646
HMT018 Hematopoietic Stem Cell Transplantation 29 0.062
647
c GLM039 Glomerulosclerosis, Focal Segmental, 6 28 0.062
648
DFN039 Deafness-Infertility Syndrome 27 0.062
649
PDT001 Pediatric Lymphoma 25 0.062
650
MYC019 Mycobacterium Marinum 25 0.062
651
GLT019 Glut1 Deficiency Syndrome 2 24 0.062
652
HMG015 Hemoglobin S Beta-Thalassemia 22 0.062
653
10P002 10p11.21p12.31 Microdeletion Syndrome 15 0.062
654
P OBS005 Obesity 93 0.060
655
ADN001 Adenosine Deaminase Deficiency 76 0.060
656
c THL005 Thalassemia 68 0.060
657
P CLN016 Colon Cancer 67 0.060
658
HYP066 Hyperglycemia 65 0.060
659
PMP001 Pemphigus 63 0.060
660
c HPT003 Hepatitis a 60 0.060
661
P PLM006 Pulmonary Alveolar Proteinosis 56 0.060
662
CLL003 Cellulitis 56 0.060
663
PRP023 Peripheral Neuropathy 53 0.060
664
CNV002 Conversion Disorder 50 0.060
665
RCR001 Recurrent Corneal Erosion 44 0.060
666
SPL006 Splenic Infarction 37 0.060
667
P MLT020 Multiple Sclerosis 82 0.059
668
P FRD001 Friedreich Ataxia 72 0.059
669
c ATM006 Autoimmune Lymphoproliferative Syndrome 68 0.059
670
c PNC044 Pancreatitis 67 0.059
671
P HRP006 Herpes Simplex 63 0.059
672
SMT015 Smith Magenis Syndrome 62 0.059
673
P MMB002 Membranous Glomerulonephritis 60 0.059
674
PLY013 Polymyalgia Rheumatica 56 0.059
675
P HML001 Hemolytic-Uremic Syndrome 54 0.059
676
TTR011 Tetraploidy 46 0.059
677
TST015 Testicular Disease 42 0.059
678
DNR001 Duane Retraction Syndrome 41 0.059
679
BRR002 Barrett's Adenocarcinoma 41 0.059
680
SML026 Small Fiber Neuropathy 37 0.059
681
PTS004 Potassium Aggravated Myotonia 20 0.059
682
P ISC010 Isochromosome Yp 14 0.059
683
c RNG015 Ring Chromosome 2 12 0.059
684
CNG034 Congestive Heart Failure 81 0.058
685
DFC004 Deficiency Anemia 66 0.058
686
P BCK002 Beckwith-Wiedemann Syndrome 65 0.058
687
P PLY019 Polyneuropathy 64 0.058
688
SQM006 Squamous Cell Carcinoma 61 0.058
689
OLF005 Olfactory Neuroblastoma 58 0.058
690
P BRG005 Brugada Syndrome 1 53 0.058
691
P BRD043 Bardet-Biedl Syndrome, Modifier of 53 0.058
692
P ALP014 Alpha-Thalassemia/mental Retardation Syndrome 52 0.058
693
DRM014 Dermatofibrosarcoma Protuberans 52 0.058
694
CYC004 Cyclic Hematopoiesis 52 0.058
695
THY089 Thymic Epithelial Neoplasm 52 0.058
696
PYD002 Pyoderma 49 0.058
697
P PST022 Posterior Uveal Melanoma 49 0.058
698
IMM060 Immunodeficiency, Common Variable, 9 46 0.058
699
LPS007 Lupus Nephritis 43 0.058
700
OLG015 Oligoarticular Juvenile Arthritis 40 0.058
701
HYP030 Hypoactive Sexual Desire Disorder 39 0.058
702
IMM020 Immunodeficiency with Hyper Igm Type 2 37 0.058
703
PLM070 Pulmonic Stenosis 37 0.058
704
GRD005 Geroderma Osteodysplasticum 36 0.058
705
MSM007 Mesomelic Dysplasia Kantaputra Type 34 0.058
706
WRN004 Wrinkly Skin Syndrome 33 0.058
707
P SVR013 Severe Congenital Neutropenia Autosomal Recessive 3 31 0.058
708
INT029 Interleukin-7 Receptor Alpha Deficiency 30 0.058
709
P SYS007 Systemic Capillary Leak Syndrome 25 0.058
710
c CHR229 Chromosome 20p Duplication 25 0.058
711
BLD025 Bladder Sarcoma 22 0.058
712
P RNL048 Renal Tubular Acidosis, Distal, Type 3 20 0.058
713
ALK017 Alk-Positive Large B-Cell Lymphoma 20 0.058
714
c DYS061 Dystonia 18 17 0.058
715
RFR007 Refractory Anemia with Excess Blasts in Transformation 15 0.058
716
P MNN012 Meningioma 79 0.056
717
NPH007 Nephrogenic Diabetes Insipidus 77 0.056
718
ULC004 Ulcerative Colitis 72 0.056
719
ADL030 Adult-Onset Still's Disease 68 0.056
720
DRM006 Dermatitis 68 0.056
721
EXT034 Extrinsic Allergic Alveolitis 65 0.056
722
NRN002 Neuronitis 64 0.056
723
P ANP001 Anaplastic Large Cell Lymphoma 61 0.056
724
c SBC007 Subacute Thyroiditis 58 0.056
725
GST027 Gastric Lymphoma 56 0.056
726
ATX019 Ataxia with Vitamin E Deficiency 55 0.056
727
FNC040 Fanconi Bickel Syndrome 54 0.056
728
LMB002 Lambert-Eaton Myasthenic Syndrome 54 0.056
729
SPL004 Splenic Marginal Zone Lymphoma 53 0.056
730
P FNC044 Fanconi Anemia, Complementation Group C 52 0.056
731
FLL013 Follicular Dendritic Cell Sarcoma 51 0.056
732
CHR370 Chronic Granulomatous Disease, Autosomal, Due to Deficiency of Cyba 50 0.056
733
THR079 Thromboembolism 50 0.056
734
PSD002 Pseudotumor Cerebri 47 0.056
735
INT146 Intervertebral Disc Disease 47 0.056
736
NDL013 Nodular Regenerative Hyperplasia 42 0.056
737
BLD054 Blood Protein Disease 41 0.056
738
HTL002 Htlv-1 Associated Myelopathy 38 0.056
739
c ERY013 Erythrocytosis 37 0.056
740
BCT015 Bacteremia 37 0.056
741
RHM014 Rheumatoid Vasculitis 35 0.056
742
CTN026 Cutaneous Neuroendocrine Carcinoma 35 0.056
743
HMC014 Homocysteinemia 35 0.056
744
PST055 Postural Hypotension 33 0.056
745
WBR001 Weber Syndrome 33 0.056
746
MLG041 Malignant Triton Tumor 32 0.056
747
PTT041 Pituitary Stalk Interruption Syndrome 30 0.056
748
DNG004 Dengue Fever, Protection Against 29 0.056
749
DYS036 Dysequilibrium Syndrome 28 0.056
750
PHS016 Phosphorylase Kinase Deficiency of Liver and Muscle, Autosomal Recessive 26 0.056
751
OST085 Osteosarcoma, Somatic 24 0.056
752
HMG012 Hemoglobin Constant Spring 21 0.056
753
OKT001 Okt4 Epitope Deficiency 19 0.056
754
c CHR193 Chromosome 13q Deletion 18 0.056
755
PTT043 Pituitary Hormone Deficiency, Combined, 6 17 0.056
756
AMY016 Amyopathic Dermatomyositis 17 0.056
757
c CHR189 Chromosome 12p Deletion 13 0.056
758
CHR458 Chromosome 9 Inversion 8 0.056
759
CRH001 Crohn's Disease 83 0.055
760
FLT001 Felty's Syndrome 62 0.055
761
TNS005 Tonsillitis 62 0.055
762
HYP014 Hyperuricemia 61 0.055
763
URT039 Urticaria 61 0.055
764
P LPS002 Liposarcoma 61 0.055
765
CRY005 Cryptococcosis 57 0.055
766
PRC013 Pericarditis 57 0.055
767
RTN003 Retinal Ischemia 56 0.055
768
OST003 Osteonecrosis 51 0.055
769
P JVN003 Juvenile Xanthogranuloma 50 0.055
770
TXC002 Toxic Encephalopathy 48 0.055
771
MCR020 Microsporidiosis 47 0.055
772
P BCL006 B-Cell Lymphomas 47 0.055
773
UNL002 Unilateral Retinoblastoma 40 0.055
774
CDQ001 Cauda Equina Syndrome 40 0.055
775
c DBT009 Diabetes Mellitus 80 0.053
776
PCK001 Pick's Disease 74 0.053
777
c LPS004 Lupus Erythematosus 73 0.053
778
P HPT001 Hepatitis C 66 0.053
779
PLS011 Plasmacytoma 63 0.053
780
LCH002 Lichen Planus 63 0.053
781
P NRV007 Nervous System Disease 61 0.053
782
HRP004 Herpes Zoster 61 0.053
783
HYP003 Hypermethioninemia 60 0.053
784
P MLG002 Malignant Peritoneal Mesothelioma 55 0.053
785
PLM020 Pleomorphic Xanthoastrocytoma 55 0.053
786
THY009 Thyroid Lymphoma 54 0.053
787
BSL006 Basaloid Squamous Cell Carcinoma 53 0.053
788
PLM009 Pleomorphic Adenoma Carcinoma 51 0.053
789
OTS002 Otospondylomegaepiphyseal Dysplasia 50 0.053
790
MYL020 Myelomeningocele 47 0.053
791
P LSS005 Lissencephaly 1 44 0.053
792
c HMR012 Hemorrhagic Fever 44 0.053
793
P PRM012 Primary Polycythemia 43 0.053
794
HYP266 Hypoxia 43 0.053
795
MYX013 Myxofibrosarcoma 43 0.053
796
MNC006 Monoclonal Gammopathy of Uncertain Significance 42 0.053
797
P MBS002 Moebius Syndrome 42 0.053
798
END021 Endomyocardial Fibrosis 42 0.053
799
RTC005 Reticulosarcoma 42 0.053
800
P ATS017 Autosomal Dominant Pseudohypoaldosteronism Type 1 40 0.053
801
CLR034 Colorectal Cancer, Somatic 40 0.053
802
c LNG047 Long Qt Syndrome 2 40 0.053
803
PHY007 Phyllode Tumor 38 0.053
804
DFF016 Diffuse Astrocytoma 37 0.053
805
ACT093 Actinic Cheilitis 37 0.053
806
c PRT070 Peritoneal Carcinoma 37 0.053
807
PLY010 Polyclonal Hypergammaglobulinemia 37 0.053
808
GBL002 Goblet Cell Carcinoid 37 0.053
809
DHY007 Dihydropteridine Reductase Deficiency 34 0.053
810
PLY100 Polyploidy 33 0.053
811
PTL001 Patulous Eustachian Tube 30 0.053
812
ECT004 Ecthyma 30 0.053
813
CRN061 Corneal Dystrophy Avellino Type 29 0.053
814
BWN003 Bowenoid Papulosis 29 0.053
815
c PLM071 Pulmonary Surfactant Metabolism Dysfunction 28 0.053
816
HYP226 Hyporeninemic Hypoaldosteronism 27 0.053
817
NCR009 Necrobiotic Xanthogranuloma 24 0.053
818
HRD111 Hereditary Persistence of Fetal Hemoglobin - Sickle Cell Disease 24 0.053
819
PYR016 Pyridoxine Deficiency 21 0.053
820
c CHR268 Chromosome 8q Duplication 19 0.053
821
c TTR021 Tetrasomy 21 18 0.053
822
EHL006 Ehlers–danlos Syndrome 11 0.053
823
c KNB001 Knobloch Syndrome 11 0.053
824
P AMY001 Amyotrophic Lateral Sclerosis 100 0.052
825
P WSK001 Wiskott-Aldrich Syndrome 87 0.052
826
P HYP075 Hypertension 86 0.052
827
TBR010 Tuberculosis 84 0.052
828
GLN003 Glanzmann's Thrombasthenia 80 0.052
829
P MYS003 Myasthenia Gravis 79 0.052
830
OMN001 Omenn Syndrome 72 0.052
831
c SRC013 Sarcoidosis 69 0.052
832
c NPH012 Nephrotic Syndrome 66 0.052
833
c ACT027 Acute Pancreatitis 63 0.052
834
CTN014 Cutaneous Mastocytosis 58 0.052
835
P INF032 Infertility 56 0.052
836
P RPD001 Rapidly Progressive Glomerulonephritis 55 0.052
837
PRC012 Pericardial Effusion 54 0.052
838
MMB001 Membranoproliferative Glomerulonephritis 53 0.052
839
CLC001 Calciphylaxis 52 0.052
840
MHC001 Mhc Class Ii Deficiency 43 0.052
841
SVR029 Severe Combined Immunodeficiency, T Cell-Negative, B-Cell/natural Killer-Cell Positive 42 0.052
842
XLN003 X-Linked Sideroblastic Anemia with Ataxia 38 0.052
843
MTR001 Mature Cataract 34 0.052
844
c RNL065 Renal Cell Carcinoma, Papillary, 1 30 0.052
845
FSR001 Fusariosis 26 0.052
846
BCL003 B-Cell Lymphocytic Neoplasm 22 0.052
847
ARG006 Aregenerative Anemia 11 0.052
848
P SYS001 Systemic Lupus Erythematosus 87 0.050
849
P MLG075 Malignant Mesothelioma 69 0.050
850
P ANR007 Anorexia Nervosa 67 0.050
851
GLB015 Glioblastoma Multiforme 64 0.050
852
CCT002 Cicatricial Pemphigoid 64 0.050
853
PRT002 Paratyphoid Fever 62 0.050
854
P RNL014 Renal Cell Carcinoma 59 0.050
855
RSC001 Rosacea 57 0.050
856
GYN001 Gynecomastia 57 0.050
857
OST019 Osteosclerosis 56 0.050
858
P CNT005 Central Nervous System Lymphoma 56 0.050
859
PNN001 Panniculitis 53 0.050
860
FML026 Familial Lipoprotein Lipase Deficiency 52 0.050
861
c PRL003 Proliferative Glomerulonephritis 52 0.050
862
HYP025 Hyperphosphatemia 50 0.050
863
GST014 Gastrointestinal Lymphoma 49 0.050
864
c BNG032 Benign Mesothelioma 46 0.050
865
c ACT135 Acute Graft Versus Host Disease 46 0.050
866
P MLG081 Malignant Teratoma 46 0.050
867
LYM052 Lymphomatoid Papulosis 43 0.050
868
PRM163 Primary Mediastinal Large B-Cell Lymphoma 43 0.050
869
VLV044 Vulvar Intraepithelial Neoplasia 42 0.050
870
c WLM002 Wilms Tumor 41 0.050
871
MCR191 Microscopic Colitis 40 0.050
872
SZR001 Sezary's Disease 40 0.050
873
P PRV002 Periventricular Nodular Heterotopia 39 0.050
874
PLS025 Plasmablastic Lymphoma 38 0.050
875
PRT082 Preterm Premature Rupture of the Membranes 38 0.050
876
c HRD045 Hereditary Hemorrhagic Telangiectasia Type 2 38 0.050
877
TXC012 Toxic Epidermal Necrolysis 38 0.050
878
OST028 Osteochondroma 37 0.050
879
ADS002 Adie Syndrome 33 0.050
880
CD4001 Cd45 Deficiency 31 0.050
881
c GLY026 Glycogen Storage Disease Type 13 31 0.050
882
c SPN183 Spontaneous Pneumothorax 31 0.050
883
c GLY025 Glycogen Storage Disease Type 12 29 0.050
884
CHR084 Chromosomal Disease 28 0.050
885
MDS018 Mediastinal Cancer 26 0.050
886
PNM003 Pneumatosis Cystoides Intestinalis 26 0.050
887
LNR006 Linear Iga Disease 25 0.050
888
c MLG088 Malignant Germ Cell Tumor 25 0.050
889
c CHR209 Chromosome 17p Duplication 24 0.050
890
GLY054 Glycogen Storage Disease Due to Phosphorylase Kinase Deficiency 23 0.050
891
MLD012 Melioidosis, Susceptibilty to 21 0.050
892
MYL015 Myeloproliferative Disorder with Eosinophilia 20 0.050
893
RDT006 Radiation Induced Meningioma 19 0.050
894
AND005 Androgen Insensitivity Syndrome, Mild 18 0.050
895
c WLM005 Wilms Tumor 2 18 0.050
896
SVR037 Severe Combined Immune Deficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative, Jak3-Related 17 0.050
897
3Q2002 3q21q26 Syndrome 16 0.050
898
c SZR011 Seizures, Benign Familial Infantile, 4 15 0.050
899
TNF006 Tnfrsf13b-Related Common Variable Immune Deficiency 14 0.050
900
CMV001 Cmv Antenatal Infection 13 0.050
901
PRM132 Primary Cutaneous Cd4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma 12 0.050
902
c PLM064 Pulmonary Sequestration 11 0.050
903
MDL007 Medial Medullary Syndrome 10 0.050
904
P GST019 Gastrointestinal Stromal Tumor 83 0.049
905
SKN016 Skin Disease 75 0.049
906
DBT011 Diabetic Retinopathy 73 0.049
907
GST023 Gastric Ulcer 72 0.049
908
c BTT002 Beta Thalassemia 70 0.049
909
KLN001 Klinefelter's Syndrome 67 0.049
910
P OLG002 Oligodendroglioma 67 0.049
911
HYP056 Hypoglycemia 66 0.049
912
CRM001 Crimean-Congo Hemorrhagic Fever 64 0.049
913
CRY004 Cryoglobulinemia 61 0.049
914
P MYP004 Myopathy 58 0.049
915
PGM001 Pigmented Villonodular Synovitis 57 0.049
916
PRT039 Proteinuria 57 0.049
917
MLT006 Multidrug-Resistant Tuberculosis 56 0.049
918
P BRN009 Burning Mouth Syndrome 56 0.049
919
P EXN002 Exanthem 53 0.049
920
SPN035 Spindle Cell Sarcoma 53 0.049
921
CRD001 Cardiac Tamponade 52 0.049
922
FSC004 Fasciitis 50 0.049
923
LCT001 Lactic Acidosis 49 0.049
924
CLN015 Colon Adenocarcinoma 48 0.049
925
GTP003 Gtp Cyclohydrolase I Deficiency 46 0.049
926
HRD024 Hereditary Persistence of Fetal Hemoglobin 44 0.049
927
SPN006 Spindle Cell Lipoma 43 0.049
928
VNS009 Venous Thrombosis 43 0.049
929
NM001 Noma 42 0.049
930
PYG006 Pyogenic Granuloma 41 0.049
931
INT221 Intravascular Large B-Cell Lymphoma 40 0.049
932
ISL003 Isolated Growth Hormone Deficiency 39 0.049
933
15Q001 15q13.3 Microdeletion 37 0.049
934
CMP001 Composite Lymphoma 36 0.049
935
P TYP024 Type Ii Mixed Cryoglobulinemia 36 0.049
936
PTT021 Pituitary Hormone Deficiency, Combined 2 36 0.049
937
BNM001 Bone Marrow Cancer 36 0.049
938
c ACQ014 Acquired Hemophilia 35 0.049
939
c LNG053 Long Qt Syndrome 9 35 0.049
940
ACN014 Acanthocytosis 32 0.049
941
MRK002 Marek Disease 31 0.049
942
GRF001 Graft-Versus-Host Disease, Protection Against 30 0.049
943
IMR001 Imerslund-Grasbeck Syndrome 29 0.049
944
EXT052 Extraskeletal Ewing Sarcoma 28 0.049
945
LMB010 Lambert Syndrome 27 0.049
946
c MLG036 Malignant Spiradenoma 26 0.049
947
16Q001 16q24.3 Microdeletion Syndrome 25 0.049
948
HPT070 Hepatosplenic T-Cell Lymphoma 24 0.049
949
TST021 Testicular Germ Cell Tumor 22 0.049
950
IDP033 Idiopathic Edema 20 0.049
951
CYT017 Cytophagic Histiocytic Panniculitis 17 0.049
952
AMY010 Amyloidosis Beta2m 16 0.049
953
TRN028 Transient Acantholytic Dermatosis 14 0.049
954
SML025 Small Non-Cleaved Cell Lymphoma 14 0.049
955
SPS044 Spastic Paraplegia Epilepsy Mental Retardation 12 0.049
956
c CLR075 Colorectal Cancer 3 9 0.049
957
c PSD024 Pseudo Pelger-Huet Anomaly 5 0.049
958
P RBN001 Rubinstein-Taybi Syndrome 78 0.047
959
P CRN008 Carney Complex 78 0.047
960
LKC001 Leukocyte Adhesion Deficiency 70 0.047
961
P FCL005 Focal Segmental Glomerulosclerosis 70 0.047
962
P ATM003 Autoimmune Thyroiditis 70 0.047
963
BRN028 Brain Cancer 67 0.047
964
P SLV002 Salivary Gland Cancer 58 0.047
965
LYM027 Lymphopenia 58 0.047
966
MRG003 Marginal Zone B-Cell Lymphoma 53 0.047
967
c JBR001 Joubert Syndrome 51 0.047
968
MHC002 Mhc Class I Deficiency 49 0.047
969
c ACT078 Acute Porphyria 48 0.047
970
c AFB001 Afibrinogenemia 48 0.047
971
GLS007 Glossitis 47 0.047
972
LNG017 Lung Giant Cell Carcinoma 47 0.047
973
LDP002 Lead Poisoning 43 0.047
974
P OMP004 Omphalocele 42 0.047
975
MCR037 Macroglossia 41 0.047
976
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 37 0.047
977
LWR010 Low Renin Hypertension 34 0.047
978
THL010 Thalassemia Minor 33 0.047
979
ADN027 Adenomyosis 32 0.047
980
c OVR069 Ovarian Germ Cell Tumor 32 0.047
981
FCT022 Factor Xi Deficiency, Autosomal Recessive 29 0.047
982
c MNS008 Monosomy 21 22 0.047
983
ENG004 Engraftment Syndrome 21 0.047
984
c HMP017 Hemophilia a, Congenital 21 0.047
985
c CHR271 Chromosome 9q Deletion 19 0.047
986
PLM111 Pleomorphic Undifferentiated Sarcoma 17 0.047
987
SBL004 Sea-Blue Histiocytosis 17 0.047
988
AGR001 Age Related Macular Degeneration 83 0.045
989
BLM001 Bloom Syndrome 82 0.045
990
MNK001 Menkes Disease 81 0.045
991
INF030 Infectious Mononucleosis 78 0.045
992
P FML018 Familial Mediterranean Fever 74 0.045
993
P BLD042 Bladder Carcinoma 73 0.045
994
PLL001 Pallister-Hall Syndrome 71 0.045
995
MYS005 Myositis 67 0.045
996
TRG002 Trigeminal Neuralgia 63 0.045
997
GLL022 Guillain-Barre Syndrome 63 0.045
998
LST001 Listeriosis 62 0.045
999
P PTT014 Pitt-Hopkins Syndrome 59 0.045
1000
INT051 Intussusception 59 0.045
1001
P SYN007 Synovitis 59 0.045
1002
GNG002 Ganglioneuroma 57 0.045
1003
ORL005 Oral Candidiasis 55 0.045
1004
PRP007 Priapism 55 0.045
1005
LPC002 Lip Cancer 55 0.045
1006
MLL005 Miller-Dieker Syndrome 52 0.045
1007
P LPR012 Leopard Syndrome 1 52 0.045
1008
BRN018 Borna Disease 51 0.045
1009
INF034 Infective Endocarditis 50 0.045
1010
BLT006 Bilateral Breast Cancer 50 0.045
1011
MLK003 Melkersson-Rosenthal Syndrome 48 0.045
1012
c CHR048 Chronic Rhinitis 43 0.045
1013
PRM097 Primary Immunodeficiency Disease 40 0.045
1014
TLY001 T Lymphocyte Deficiency 40 0.045
1015
INT071 Intestinal Perforation 39 0.045
1016
PRL008 Paralytic Ileus 39 0.045
1017
SRC015 Sarcosinemia 36 0.045
1018
P CRN074 Coronary Artery Aneurysm 34 0.045
1019
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 34 0.045
1020
NRW001 Norwegian Scabies 29 0.045
1021
BNM005 Bone Marrow Necrosis 27 0.045
1022
MYL002 Myelophthisic Anemia 25 0.045
1023
GRN011 Granulomatous Gastritis 20 0.045
1024
P MYC007 Myocardial Infarction 88 0.044
1025
PRC016 Pre-Eclampsia 75 0.044
1026
KWS002 Kawasaki Disease 74 0.044
1027
SCK003 Sickle Cell Anemia 73 0.044
1028
P CLR023 Colorectal Cancer 73 0.044
1029
PRC002 Paracoccidioidomycosis 70 0.044
1030
P PRT010 Parathyroid Carcinoma 69 0.044
1031
P NNN008 Noonan Syndrome 1 69 0.044
1032
c PRM002 Primary Hyperoxaluria 68 0.044
1033
PLY017 Polyarteritis Nodosa 68 0.044
1034
ADN018 Adenoma 67 0.044
1035
P HRD011 Hereditary Spherocytosis 66 0.044
1036
P AGM001 Agammaglobulinemia 61 0.044
1037
c ACT075 Acute Myocardial Infarction 61 0.044
1038
P CNJ013 Conjunctivitis 61 0.044
1039
EPD006 Epidermolysis Bullosa Acquisita 61 0.044
1040
BRN002 Bronchiolitis 61 0.044
1041
MLT001 Multiple Chemical Sensitivity 59 0.044
1042
BRN012 Bronchiolitis Obliterans 59 0.044
1043
P MMP001 Mumps 59 0.044
1044
NNS005 Non-Small Cell Lung Carcinoma 58 0.044
1045
P PRT008 Proteus Syndrome 56 0.044
1046
APP001 Apparent Mineralocorticoid Excess Syndrome 56 0.044
1047
ADN009 Adenosquamous Carcinoma 55 0.044
1048
CLC006 Calcinosis 55 0.044
1049
CHC001 Chickenpox 54 0.044
1050
ART008 Arteriosclerosis Obliterans 53 0.044
1051
CRN030 Coronary Stenosis 53 0.044
1052
TCL003 T Cell Deficiency 52 0.044
1053
PTT004 Pituitary Apoplexy 51 0.044
1054
SCB001 Scabies 51 0.044
1055
HYP005 Hypokalemia 50 0.044
1056
PST010 Pasteurellosis 50 0.044
1057
IDP064 Idiopathic Neutropenia 50 0.044
1058
HMH002 Hemihypertrophy 50 0.044
1059
FRZ001 Frozen Shoulder 49 0.044
1060
c MLR021 Malaria, Severe 49 0.044
1061
MST001 Mast-Cell Sarcoma 49 0.044
1062
GLN002 Glanders 48 0.044
1063
c CNG027 Congenital Hemolytic Anemia 48 0.044
1064
P ATM029 Autoimmune Lymphoproliferative Syndrome, Type Ib 46 0.044
1065
SLT008 Solitary Fibrous Tumor 46 0.044
1066
LBL001 Lobular Neoplasia 44 0.044
1067
ETH009 Ethmoid Sinusitis 44 0.044
1068
c GLY023 Glycogen Storage Disease Type 0 43 0.044
1069
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 42 0.044
1070
MCR014 Microcystic Adenoma 40 0.044
1071
NNL002 Nonalcoholic Steatohepatitis 39 0.044
1072
RHB017 Rhabdoid Tumor 38 0.044
1073
DFF024 Diffuse Panbronchiolitis 38 0.044
1074
c LNG063 Lung Cancer Susceptibility 38 0.044
1075
c HMC010 Hemochromatosis, Type 3 38 0.044
1076
INF058 Inflammatory Myofibroblastic Tumor 37 0.044
1077
WRT003 Warthin Tumor 36 0.044
1078
CTS005 Catastrophic Antiphospholipid Syndrome 35 0.044
1079
c ART070 Aortic Valve Disease 34 0.044
1080
FST010 Fasting Hypoglycemia 32 0.044
1081
BRD025 Birdshot Chorioretinopathy 31 0.044
1082
MTG002 Mutagen Sensitivity 31 0.044
1083
ENC014 Enchondroma 31 0.044
1084
END048 Endotoxin Hyporesponsiveness 31 0.044
1085
BRR005 Barraquer-Simons Syndrome 30 0.044
1086
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 30 0.044
1087
P MYP018 Myopia 6 29 0.044
1088
P ALP005 Alpha Chain Disease 29 0.044
1089
HVD003 Hiv/aids 29 0.044
1090
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 28 0.044
1091
SPL007 Splenic Abscess 28 0.044
1092
c ACT053 Acute Thyroiditis 28 0.044
1093
MNN034 Mannose-Binding Lectin Deficiency 28 0.044
1094
MCR125 Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related 28 0.044
1095
ENT007 Enteropathica 27 0.044
1096
c GLT013 Glutaric Acidemia Type Ii 26 0.044
1097
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 25 0.044
1098
c HPT073 Hepatitis C Virus 25 0.044
1099
PTY004 Pityriasis Lichenoides 25 0.044
1100
P MYC023 Myoclonic Astatic Epilepsy 25 0.044
1101
CVR010 Cavernous Malformation 23 0.044
1102
RMR001 Ramer Ladda Syndrome 23 0.044
1103
CNG101 Congenital Human Immunodeficiency Virus 20 0.044
1104
CHR176 Chromophil Renal Cell Carcinoma 18 0.044
1105
ACT176 Acute Panmyelosis with Myelofibrosis 17 0.044
1106
THY020 Thyroid Hyalinizing Trabecular Adenoma 17 0.044
1107
SPS082 Spastic Paraplegia - Epilepsy - Intellectual Deficit 16 0.044
1108
OTP003 Oto-Palatal-Digital Syndrome 13 0.044
1109
c CHR237 Chromosome 2p Deletion 12 0.044
1110
c ENG003 Eng-Related Hereditary Hemorrhagic Telangiectasia 11 0.044
1111
EXF003 Exfoliative Dermatitis 10 0.044
1112
PRV008 Parvovirus Antenatal Infection 9 0.044
1113
c CHR257 Chromosome 6q Deletion 8 0.044
1114
VNH001 Von Hippel-Lindau Disease 89 0.042
1115
P OST018 Osteosarcoma 81 0.042
1116
CLD001 Cleidocranial Dysplasia 78 0.042
1117
P AST007 Astrocytoma 72 0.042
1118
PMS001 Poems Syndrome 67 0.042
1119
P DGR001 Digeorge Syndrome 67 0.042
1120
P RHN004 Rhinitis 65 0.042
1121
HPT022 Hepatoblastoma 65 0.042
1122
c ENC004 Encephalitis 64 0.042
1123
c MCP010 Mucopolysaccharidosis 61 0.042
1124
PSR002 Psoriasis 60 0.042
1125
INT075 Intracranial Hypertension 59 0.042
1126
PRM027 Primitive Neuroectodermal Tumor 59 0.042
1127
NTR001 Neutral Lipid Storage Disease 59 0.042
1128
LYM021 Lymphadenitis 58 0.042
1129
P MGL001 Megaloblastic Anemia 55 0.042
1130
DND002 Dendritic Cell Sarcoma 54 0.042
1131
BCL002 B Cell Deficiency 53 0.042
1132
HYP017 Hypophosphatemia 53 0.042
1133
IMM001 Immune-Complex Glomerulonephritis 50 0.042
1134
P CHR019 Choroid Plexus Carcinoma 50 0.042
1135
FCL012 Facial Paralysis 49 0.042
1136
AGG002 Aggressive Systemic Mastocytosis 47 0.042
1137
c CNG003 Congenital Dyserythropoietic Anemia 44 0.042
1138
CYT005 Cytomegalovirus Retinitis 42 0.042
1139
INT052 Intestinal Volvulus 42 0.042
1140
P WLM008 Wilms Tumor, Type 1 39 0.042
1141
c PRM051 Primary Pigmented Nodular Adrenocortical Disease 37 0.042
1142
VRL011 Viral Infectious Disease 37 0.042
1143
CLL005 Cellular Leiomyoma 33 0.042
1144
MN1001 Mn1 32 0.042
1145
c CHR091 Chronic Meningitis 29 0.042
1146
GNR008 Generalized Resistance to Thyroid Hormone 27 0.042
1147
c CLD010 Cold-Induced Sweating Syndrome 1 16 0.042
1148
WLS001 Wilson Disease 89 0.040
1149
KPS001 Kaposi's Sarcoma 87 0.040
1150
P HNT001 Huntington's Disease 87 0.040
1151
P HMC003 Hemochromatosis 80 0.040
1152
P OST002 Osteoporosis 77 0.040
1153
LSH001 Leishmaniasis 74 0.040
1154
TKY001 Takayasu's Arteritis 72 0.040
1155
VSC007 Vascular Disease 72 0.040
1156
P LVR013 Liver Disease 70 0.040
1157
P TMP003 Temporal Arteritis 69 0.040
1158
P DDN001 Duodenal Ulcer 68 0.040
1159
P RTH001 Rothmund-Thomson Syndrome 67 0.040
1160
ANT006 Antiphospholipid Syndrome 67 0.040
1161
P PRT013 Portal Hypertension 67 0.040
1162
c JVN010 Juvenile Rheumatoid Arthritis 67 0.040
1163
P AMY004 Amyloidosis 65 0.040
1164
AMN001 Amenorrhea 63 0.040
1165
c TXP001 Toxoplasmosis 62 0.040
1166
PPL002 Papillary Carcinoma 61 0.040
1167
WLF002 Wolf-Hirschhorn Syndrome 60 0.040
1168
P RTN022 Retinal Vein Occlusion 59 0.040
1169
NRH001 Neurohypophyseal Diabetes Insipidus 58 0.040
1170
ANT011 Antisocial Personality Disorder 57 0.040
1171
P END047 Endophthalmitis 56 0.040
1172
HYP068 Hyperostosis 56 0.040
1173
c THR003 Thoracic Aortic Aneurysm 56 0.040
1174
SPN020 Spondylosis 54 0.040
1175
GST050 Gastrointestinal System Disease 54 0.040
1176
ACT008 Actinic Keratosis 53 0.040
1177
c CNT016 Central Retinal Vein Occlusion 53 0.040
1178
PLR008 Pleurisy 53 0.040
1179
PLY020 Polyradiculoneuropathy 52 0.040
1180
PRN011 Pernicious Anemia 52 0.040
1181
THY022 Thymic Carcinoma 51 0.040
1182
DYS006 Dysembryoplastic Neuroepithelial Tumor 48 0.040
1183
JCB001 Jacobsen Syndrome 48 0.040
1184
c ADN012 Adenocarcinoma in Situ 48 0.040
1185
PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 48 0.040
1186
P MGL002 Megalencephalic Leukoencephalopathy with Subcortical Cysts 48 0.040
1187
RTN001 Retinal Vasculitis 47 0.040
1188
P PRM126 Primary Peritoneal Carcinoma 47 0.040
1189
GRN007 Granuloma Annulare 47 0.040
1190
c CNG029 Congenital Mesoblastic Nephroma 45 0.040
1191
P PRK001 Porokeratosis 45 0.040
1192