Search results for Tacrolimus

809 hits were found for Tacrolimus

# Family MCID Name MIFTS Score
1
TCR004 Tacrolimus Dose Selection 13 2.894
2
IMM158 Immune Suppression 57 0.428
3
P GRF003 Graft-Versus-Host Disease 72 0.370
4
P KDN018 Kidney Disease 69 0.359
5
HML018 Homologous Wasting Disease 18 0.346
6
P LKM002 Leukemia 75 0.327
7
HMT018 Hematopoietic Stem Cell Transplantation 58 0.317
8
URN009 Urinary System Disease 58 0.309
9
P LYM118 Lymphoma 71 0.297
10
IMM136 Immune System Disease 57 0.296
11
c ACT135 Acute Graft Versus Host Disease 57 0.294
12
LYM019 Lymphosarcoma 58 0.293
13
P MYL006 Myeloid Leukemia 69 0.293
14
MYL009 Myelodysplastic Syndrome 75 0.290
15
LYM024 Lymphatic System Disease 45 0.282
16
c LKM061 Leukemia, Acute Myeloid 81 0.277
17
ACT118 Acute Non Lymphoblastic Leukemia 32 0.276
18
P LYM026 Lymphoblastic Leukemia 66 0.274
19
LYM067 Lymphoid Leukemia 43 0.274
20
MYL031 Myeloproliferative Neoplasm 64 0.258
21
c CHR417 Chronic Graft Versus Host Disease 65 0.256
22
c LKM062 Leukemia, Acute Lymphoblastic 64 0.252
23
P ACT074 Acute Lymphocytic Leukemia 61 0.252
24
c LKM063 Leukemia, Chronic Myeloid 80 0.250
25
DRM006 Dermatitis 67 0.248
26
ATM095 Autoimmune Disease 66 0.236
27
LYM133 Lymphoma, Hodgkin, Classic 78 0.234
28
VRL011 Viral Infectious Disease 64 0.232
29
MYL069 Myeloma, Multiple 86 0.231
30
PLS009 Plasma Cell Neoplasm 51 0.231
31
c LKM071 Leukemia, Chronic Lymphocytic 75 0.230
32
c LKM004 Leukemia, B-Cell, Chronic 37 0.230
33
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.229
34
P HMR003 Hemorrhagic Disease 61 0.228
35
P BLD051 Blood Coagulation Disease 38 0.228
36
VSC008 Vascular Hemostatic Disease 36 0.225
37
P DRM053 Dermatitis, Atopic 68 0.217
38
HDG004 Hodgkin's Granuloma 28 0.211
39
HDG006 Hodgkin's Paragranuloma 21 0.211
40
HMT002 Hematologic Cancer 64 0.204
41
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.200
42
P FLL037 Follicular Lymphoma 76 0.197
43
DFF005 Diffuse Large B-Cell Lymphoma 64 0.197
44
MNT001 Mantle Cell Lymphoma 76 0.196
45
P BCL006 B-Cell Lymphomas 70 0.194
46
c CHR089 Chronic Kidney Failure 72 0.193
47
CNN005 Connective Tissue Disease 65 0.188
48
P LPS004 Lupus Erythematosus 69 0.187
49
SKN016 Skin Disease 68 0.187
50
P HPT021 Hepatitis 75 0.185
51
P GLM007 Glomerulonephritis 61 0.185
52
RTC009 Reticulum Cell Sarcoma 51 0.185
53
RTC005 Reticulosarcoma 49 0.185
54
INT038 Interdigitating Dendritic Cell Sarcoma 46 0.185
55
SKN027 Skin Conditions 48 0.184
56
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.182
57
P MYL005 Myelofibrosis 75 0.181
58
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 67 0.179
59
MRG003 Marginal Zone B-Cell Lymphoma 56 0.179
60
LYM040 Lymphoblastic Lymphoma 58 0.178
61
P LVR013 Liver Disease 76 0.176
62
c JVN004 Juvenile Myelomonocytic Leukemia 70 0.176
63
P CHR285 Chronic Myelomonocytic Leukemia 63 0.176
64
P NPH012 Nephrotic Syndrome 60 0.176
65
BRK010 Burkitt Lymphoma 71 0.173
66
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 36 0.171
67
RFR001 Refractory Plasma Cell Neoplasm 19 0.171
68
PLS025 Plasmablastic Lymphoma 51 0.168
69
NDL020 Nodal Marginal Zone B-Cell Lymphoma 38 0.168
70
LYM048 Lymphoma, Large-Cell, Immunoblastic 31 0.168
71
END030 End Stage Renal Failure 59 0.166
72
SPL004 Splenic Marginal Zone Lymphoma 52 0.164
73
P DBT009 Diabetes Mellitus 72 0.163
74
c HPT003 Hepatitis a 63 0.163
75
PLS011 Plasmacytoma 60 0.161
76
c HPT001 Hepatitis C 73 0.152
77
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.150
78
c HPT073 Hepatitis C Virus 73 0.148
79
KRT006 Keratoconjunctivitis 56 0.148
80
P WLD002 Waldenstrom Macroglobulinemia 65 0.144
81
MCR004 Macroglobulinemia 54 0.144
82
LYM012 Lymphoplasmacytic Lymphoma 50 0.144
83
GST050 Gastrointestinal System Disease 66 0.142
84
P ART022 Arthritis 77 0.140
85
ATY042 Atypical Chronic Myeloid Leukemia 51 0.136
86
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 62 0.132
87
P CTN015 Cutaneous T Cell Lymphoma 56 0.132
88
P RHM011 Rheumatoid Arthritis 91 0.130
89
MYC006 Mycosis Fungoides 73 0.128
90
SZR001 Sezary's Disease 58 0.128
91
P LCH002 Lichen Planus 58 0.128
92
GLC008 Glucose Metabolism Disease 38 0.128
93
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.128
94
HDG009 Hodgkin Lymphoma, Childhood 20 0.128
95
LNG099 Lung Disease 67 0.123
96
P TCL004 T-Cell Leukemia 50 0.123
97
LCH009 Lichen Sclerosus 45 0.121
98
c ADL017 Adult T-Cell Leukemia 63 0.119
99
P MMB011 Membranous Nephropathy 55 0.119
100
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 28 0.119
101
LYM051 Lymphomatoid Granulomatosis 51 0.116
102
P RFR008 Refractory Anemia with Excess Blasts 34 0.116
103
c LKM005 Leukemia, T-Cell, Chronic 25 0.116
104
APL001 Aplastic Anemia 74 0.114
105
ORL013 Oral Lichen Planus 51 0.114
106
SML025 Small Non-Cleaved Cell Lymphoma 25 0.114
107
VSC007 Vascular Disease 71 0.111
108
P EXN002 Exanthem 62 0.111
109
VRN004 Vernal Keratoconjunctivitis 56 0.111
110
CHR563 Chronic Eosinophilic Leukemia 51 0.111
111
CHR286 Chronic Neutrophilic Leukemia 49 0.111
112
RFR010 Refractory Anemia 48 0.111
113
ARG006 Aregenerative Anemia 26 0.111
114
P ANP001 Anaplastic Large Cell Lymphoma 60 0.109
115
HRY003 Hairy Cell Leukemia 60 0.109
116
RFR002 Refractory Hairy Cell Leukemia 32 0.109
117
CLS052 Classic Hairy Cell Leukemia 16 0.109
118
ULC004 Ulcerative Colitis 80 0.106
119
P CNJ013 Conjunctivitis 67 0.106
120
CLT003 Colitis 63 0.106
121
c ACT073 Acute Leukemia 61 0.106
122
P MYS003 Myasthenia Gravis 73 0.103
123
PRL017 Prolymphocytic Leukemia 51 0.101
124
LTH001 Lethal Midline Granuloma 40 0.101
125
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 29 0.101
126
PLY001 Polycythemia Vera 75 0.098
127
P ESS003 Essential Thrombocythemia 71 0.098
128
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.098
129
P ART023 Arthropathy 68 0.098
130
P DRM010 Dermatomyositis 65 0.098
131
P INT068 Intestinal Disease 65 0.098
132
GNG013 Gingivitis 64 0.098
133
RHM027 Rheumatic Disease 62 0.098
134
JNT002 Joint Disorders 60 0.098
135
P PLY018 Polycythemia 60 0.098
136
CYT008 Cytomegalovirus Infection 57 0.098
137
THR004 Thrombocytosis 55 0.098
138
P CLL015 Collagen Disease 53 0.098
139
c PRM012 Primary Polycythemia 53 0.098
140
PYD002 Pyoderma 51 0.098
141
ANG046 Angioimmunoblastic T-Cell Lymphoma 46 0.098
142
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 44 0.098
143
ENT004 Enthesopathy 38 0.098
144
DLT018 Dilution, Pigmentary 37 0.098
145
PGM003 Pigmentation Disease 36 0.098
146
CYT004 Cytomegalic Inclusion Disease 35 0.098
147
c TRC078 Trichohepatoenteric Syndrome 2 34 0.098
148
HYP213 Hypomelanotic Disorder 25 0.098
149
c SYS001 Systemic Lupus Erythematosus 86 0.095
150
P PNM007 Pneumonia 70 0.095
151
GST045 Gastroenteritis 65 0.095
152
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.095
153
P PSR002 Psoriasis 65 0.092
154
MCS002 Mucositis 61 0.092
155
P FCL005 Focal Segmental Glomerulosclerosis 60 0.092
156
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.092
157
P PLY041 Polymyositis 57 0.092
158
P TRC086 Trichohepatoenteric Syndrome 1 54 0.092
159
P INF038 Influenza 77 0.089
160
LVR012 Liver Cirrhosis 73 0.089
161
AGN016 Aging 65 0.089
162
P INF032 Infertility 59 0.089
163
GLC003 Glucose Intolerance 58 0.089
164
PYD001 Pyoderma Gangrenosum 55 0.089
165
P CTN003 Cutaneous Lupus Erythematosus 53 0.089
166
P INF037 Inflammatory Bowel Disease 52 0.089
167
GNG012 Gingival Overgrowth 52 0.089
168
c MYS011 Myasthenia Gravis Congenital 28 0.089
169
ISC004 Ischemia 66 0.086
170
P THR014 Thrombocytopenia 65 0.086
171
INT066 Interstitial Lung Disease 63 0.086
172
SPS003 Spastic Diplegia 55 0.086
173
RFR007 Refractory Anemia with Excess Blasts in Transformation 25 0.086
174
AST005 Asthma 83 0.082
175
HYP056 Hypoglycemia 62 0.082
176
ACQ007 Acquired Immunodeficiency Syndrome 65 0.079
177
PRP030 Purpura 61 0.079
178
NRM005 Neuromuscular Disease 60 0.079
179
ALL009 Allergic Conjunctivitis 53 0.079
180
STM007 Stomatitis 52 0.079
181
INT054 Intraocular Lymphoma 50 0.079
182
CNJ012 Conjunctival Disease 48 0.079
183
SML008 Small Intestine Lymphoma 45 0.079
184
CHR463 Chronic Actinic Dermatitis 34 0.079
185
P MYP004 Myopathy 69 0.075
186
P DRR001 Diarrhea 60 0.075
187
BRN002 Bronchiolitis 59 0.075
188
CLN019 Colonic Disease 55 0.075
189
TXC002 Toxic Encephalopathy 55 0.075
190
HMG005 Hemoglobinopathy 53 0.075
191
c BNG091 Benign Chronic Pemphigus 52 0.075
192
CRN024 Corneal Disease 47 0.075
193
BLD053 Blood Platelet Disease 45 0.075
194
CPL005 Capillary Disease 38 0.075
195
P HRT032 Heart Disease 80 0.071
196
MTH009 Mouth Disease 64 0.071
197
ERY003 Erythema Multiforme 60 0.071
198
BRN012 Bronchiolitis Obliterans 60 0.071
199
BRN038 Bronchial Disease 58 0.071
200
RTN018 Retinal Disease 56 0.071
201
PNC001 Pancytopenia 50 0.071
202
DSC009 Discoid Lupus Erythematosus 48 0.071
203
CHL056 Cheilitis 47 0.071
204
BLN010 Balanitis 36 0.071
205
P SCL057 Scoliosis, Isolated 1 28 0.071
206
SCK003 Sickle Cell Anemia 73 0.067
207
P ADN016 Adenocarcinoma 71 0.067
208
MGK001 Megakaryocytic Leukemia 63 0.067
209
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.067
210
P UVT001 Uveitis 61 0.067
211
OCL009 Ocular Cancer 61 0.067
212
RSC001 Rosacea 58 0.067
213
P ALP008 Alopecia 56 0.067
214
P PMP001 Pemphigus 55 0.067
215
SCK005 Sickle Cell Disease 54 0.067
216
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 53 0.067
217
ACT098 Acute Erythroid Leukemia 52 0.067
218
BNM001 Bone Marrow Cancer 52 0.067
219
PRR002 Pure Red-Cell Aplasia 52 0.067
220
LRG008 Large Granular Lymphocyte Leukemia 49 0.067
221
PRP036 Peripheral T-Cell Lymphoma 48 0.067
222
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 0.067
223
PRC003 Proctitis 44 0.067
224
TST004 Testicular Lymphoma 42 0.067
225
c BLD140 Blood Group, I System 37 0.067
226
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 25 0.067
227
ACQ031 Acquired Idiopathic Sideroblastic Anemia 24 0.067
228
CRH001 Crohn's Disease 80 0.063
229
P NRV007 Nervous System Disease 75 0.063
230
P OST002 Osteoporosis 75 0.063
231
SQM006 Squamous Cell Carcinoma 74 0.063
232
P MYS005 Myositis 63 0.063
233
THR024 Thrombosis 61 0.063
234
P MNC007 Monocytic Leukemia 59 0.063
235
P ENC018 Encephalopathy 58 0.063
236
c LKM070 Leukemia, Acute Monocytic 55 0.063
237
PNM001 Pneumocystosis 55 0.063
238
P TRM003 Tremor 54 0.063
239
MSC033 Muscle Disorders 53 0.063
240
ART140 Arteries, Anomalies of 51 0.063
241
ACT200 Acute Monoblastic Leukemia 47 0.063
242
ATP013 Atopic Keratoconjunctivitis 45 0.063
243
HPT070 Hepatosplenic T-Cell Lymphoma 43 0.063
244
LCH004 Lichen Disease 42 0.063
245
P SBR004 Seborrheic Dermatitis 40 0.063
246
MSC004 Muscle Tissue Disease 39 0.063
247
ERS002 Erosive Pustular Dermatosis of the Scalp 25 0.063
248
ULC008 Ulcerative Proctitis 24 0.063
249
c ADL093 Adult Acute Monocytic Leukemia 22 0.063
250
WRN001 Werner Syndrome 70 0.058
251
P AMY004 Amyloidosis 69 0.058
252
c HPT016 Hepatitis B 68 0.058
253
RNL114 Renal Cell Carcinoma, Nonpapillary 68 0.058
254
P KDN017 Kidney Cancer 66 0.058
255
P THL005 Thalassemia 65 0.058
256
FCT002 Factor Xi Deficiency 64 0.058
257
HYP066 Hyperglycemia 64 0.058
258
ACT119 Acute Promyelocytic Leukemia 64 0.058
259
P NRP001 Neuropathy 63 0.058
260
c ATM011 Autoimmune Hepatitis 63 0.058
261
P ART021 Arteriosclerosis 62 0.058
262
P CTR002 Cataract 60 0.058
263
P NTR004 Neutropenia 60 0.058
264
GT001 Gout 60 0.058
265
c ALM001 Al Amyloidosis 56 0.058
266
c ACT071 Acute Kidney Failure 54 0.058
267
HMG002 Hemoglobinuria 52 0.058
268
FLL008 Folliculitis 50 0.058
269
HYP077 Hypertrichosis 49 0.058
270
LPD004 Lipoid Nephrosis 46 0.058
271
ACT088 Acute Insulin Response 43 0.058
272
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.058
273
GRN007 Granuloma Annulare 40 0.058
274
ACT114 Acute Myeloblastic Leukemia Without Maturation 32 0.058
275
P BRS047 Breast Cancer 100 0.053
276
P HPT023 Hepatocellular Carcinoma 94 0.053
277
P PRS040 Prostate Cancer 88 0.053
278
P CRN018 Coronary Artery Anomaly 69 0.053
279
SRC014 Sarcoma 68 0.053
280
P ENC004 Encephalitis 66 0.053
281
CNT047 Contact Dermatitis 64 0.053
282
KRT001 Keratoconjunctivitis Sicca 63 0.053
283
MNT002 Mental Depression 60 0.053
284
c SCL052 Scleroderma, Familial Progressive 60 0.053
285
NTH001 Netherton Syndrome 60 0.053
286
P CRN300 Coronary Heart Disease 1 57 0.053
287
P CYS018 Cystitis 57 0.053
288
c INF071 Inflammatory Bowel Disease 1 54 0.053
289
ILT001 Ileitis 52 0.053
290
IDP024 Idiopathic Inflammatory Myopathy 49 0.053
291
GRN017 Granulocytopenia 49 0.053
292
EWN002 Ewing's Family of Tumors 49 0.053
293
PST011 Pustulosis of Palm and Sole 47 0.053
294
P RSM001 Rasmussen Encephalitis 46 0.053
295
PLS016 Plasma Cell Leukemia 43 0.053
296
MTS001 Mutism 42 0.053
297
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.053
298
P CHR084 Chromosomal Disease 40 0.053
299
NRM006 Neuromuscular Junction Disease 39 0.053
300
SBC017 Sebaceous Gland Disease 38 0.053
301
NCR002 Necrobiosis Lipoidica 35 0.053
302
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.053
303
LKC003 Leukocyte Disease 34 0.053
304
ACT216 Acute Leukemia of Ambiguous Lineage 30 0.053
305
ACT095 Acute Biphenotypic Leukemia 29 0.053
306
PLS003 Plasmacytic Leukemia 22 0.053
307
AML051 Aml with Myelodysplasia-Related Features 19 0.053
308
PLY043 Polyomavirus Allograft Nephropathy 11 0.053
309
BND002 B- and T-Cell Mixed Leukemia 9 0.053
310
P MLT020 Multiple Sclerosis 85 0.047
311
P MYC007 Myocardial Infarction 81 0.047
312
c MCL042 Macular Degeneration, Age-Related, 1 79 0.047
313
P WSK001 Wiskott-Aldrich Syndrome 76 0.047
314
CNG034 Congestive Heart Failure 74 0.047
315
ISC006 Ischemic Heart Disease 73 0.047
316
c BTT014 Beta-Thalassemia 70 0.047
317
P EPL164 Epilepsy 70 0.047
318
P DMN001 Diamond-Blackfan Anemia 70 0.047
319
CRB039 Cerebrovascular Disease 68 0.047
320
P SYS005 Systemic Scleroderma 67 0.047
321
c LCL006 Localized Scleroderma 66 0.047
322
VSC011 Vasculitis 66 0.047
323
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.047
324
P ALP009 Alopecia Areata 64 0.047
325
APH001 Aphthous Stomatitis 64 0.047
326
SHW002 Shwachman-Diamond Syndrome 63 0.047
327
P CND004 Candidiasis 61 0.047
328
ALL010 Allergic Contact Dermatitis 60 0.047
329
LPD008 Lipid Metabolism Disorder 59 0.047
330
SFT003 Soft Tissue Sarcoma 58 0.047
331
CRT016 Carotid Artery Disease 58 0.047
332
P RNL003 Renal Clear Cell Carcinoma 58 0.047
333
P RTN016 Retinal Degeneration 56 0.047
334
P MYP006 Myopia 56 0.047
335
HPT046 Hepatic Veno-Occlusive Disease 56 0.047
336
FDL002 Food Allergy 55 0.047
337
NRT004 Neuritis 55 0.047
338
CLR030 Clear Cell Renal Cell Carcinoma 55 0.047
339
HDC001 Headache 55 0.047
340
BRN071 Brain Injury 54 0.047
341
KRT009 Keratosis 53 0.047
342
EXT010 Extramedullary Plasmacytoma 52 0.047
343
P SML016 Small Intestine Cancer 52 0.047
344
ORL005 Oral Candidiasis 51 0.047
345
c MLG074 Malignant Mesenchymoma 51 0.047
346
DBT084 Diabetes Mellitus, Ketosis-Prone 50 0.047
347
P HML001 Hemolytic-Uremic Syndrome 50 0.047
348
CNG028 Congenital Hypoplastic Anemia 50 0.047
349
c PST005 Posterior Uveitis 50 0.047
350
DYS073 Dysphagia 47 0.047
351
ULC007 Ulcerative Stomatitis 46 0.047
352
END072 Endotheliitis 46 0.047
353
DFF003 Diffuse Scleroderma 44 0.047
354
SKN005 Skin Atrophy 41 0.047
355
c ADL027 Adult Dermatomyositis 41 0.047
356
FXF002 Fox-Fordyce Disease 40 0.047
357
PHT003 Phototoxic Dermatitis 39 0.047
358
SLT001 Solitary Osseous Plasmacytoma 39 0.047
359
P ATM020 Autoimmune Enteropathy 39 0.047
360
BLP006 Blepharoconjunctivitis 36 0.047
361
SWL001 Swallowing Disorders 36 0.047
362
LCH016 Lichen Sclerosus Et Atrophicus 36 0.047
363
RNL105 Renal Agenesis, Unilateral 35 0.047
364
ESN016 Eosinophilic Pustular Folliculitis 27 0.047
365
c BKV001 Bk-Virus Nephropathy 26 0.047
366
LCH008 Lichen Planus Pigmentosus 22 0.047
367
P AST055 Asthma-Related Traits 1 18 0.047
368
HRP008 Herpes Simiae 16 0.047
369
HPD002 Hepadnavirus Infection 14 0.047
370
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.041
371
CYS001 Cystic Fibrosis 85 0.041
372
P NRB001 Neuroblastoma 73 0.041
373
P MNN013 Meningitis 71 0.041
374
WGN006 Wegener Granulomatosis 71 0.041
375
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.041
376
BRN024 Bronchitis 67 0.041
377
P NRM001 Neuromyelitis Optica 67 0.041
378
ACR006 Aceruloplasminemia 65 0.041
379
ADL030 Adult-Onset Still's Disease 65 0.041
380
c CNT035 Central Nervous System Disease 65 0.041
381
P HYP098 Hypereosinophilic Syndrome 65 0.041
382
VLC001 Velocardiofacial Syndrome 64 0.041
383
RSP006 Respiratory System Disease 63 0.041
384
LNG108 Langerhans Cell Histiocytosis 63 0.041
385
KRT019 Keratitis, Hereditary 62 0.041
386
P HML002 Hemolytic Anemia 62 0.041
387
P PLY014 Polycystic Kidney Disease 60 0.041
388
P HST010 Histiocytosis 60 0.041
389
RGD003 Rigid Spine Muscular Dystrophy 1 59 0.041
390
BNC003 Bone Cancer 59 0.041
391
c SVR003 Severe Congenital Neutropenia 58 0.041
392
P SJG008 Sjogren Syndrome 58 0.041
393
HYP810 Hypereosinophilic Syndrome, Idiopathic 57 0.041
394
EPD016 Epidermolysis Bullosa 57 0.041
395
BRN106 Burns 57 0.041
396
PTT009 Pituitary Gland Disease 56 0.041
397
c ANM038 Anemia, Autoimmune Hemolytic 56 0.041
398
PRS042 Prostate Disease 56 0.041
399
P PMP005 Pemphigus Vulgaris 56 0.041
400
PST046 Post-Transplant Lymphoproliferative Disease 56 0.041
401
DGR001 Digeorge Syndrome 55 0.041
402
P HYP024 Hypoparathyroidism 55 0.041
403
P SZR006 Seizure Disorder 55 0.041
404
CCT002 Cicatricial Pemphigoid 54 0.041
405
PRP019 Peripheral Nervous System Disease 53 0.041
406
IGG001 Iga Glomerulonephritis 52 0.041
407
TLN003 Telangiectasis 52 0.041
408
P RNL007 Renal Tubular Acidosis 51 0.041
409
DRY001 Dry Eye Syndrome 51 0.041
410
NSD001 Nose Disease 51 0.041
411
PRT030 Parathyroid Gland Disease 50 0.041
412
RNL077 Renal Fibrosis 49 0.041
413
MNC006 Monoclonal Gammopathy of Uncertain Significance 49 0.041
414
HNC001 Henoch-Schoenlein Purpura 48 0.041
415
PNN001 Panniculitis 48 0.041
416
HDN002 Head Injury 48 0.041
417
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.041
418
SLV003 Salivary Gland Disease 47 0.041
419
LYM127 Lymphatic Malformations 45 0.041
420
PTY001 Pityriasis Rosea 45 0.041
421
MCR225 Macrophage Activation Syndrome 44 0.041
422
MLL001 Molluscum Contagiosum 43 0.041
423
CLL014 Cll/sll 43 0.041
424
LCR008 Lacrimal Apparatus Disease 43 0.041
425
CRB009 Cerebritis 41 0.041
426
LTT002 Letterer-Siwe Disease 39 0.041
427
RCT017 Rectal Disease 38 0.041
428
c MYL058 Myeloproliferative Syndrome, Transient 37 0.041
429
ORL022 Oral Erosive Lichen 36 0.041
430
CYL001 Cayler Cardiofacial Syndrome 36 0.041
431
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 36 0.041
432
c HYP072 Hypersensitivity Reaction Type Iii Disease 35 0.041
433
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 35 0.041
434
GNG006 Gingival Hypertrophy 35 0.041
435
ACR005 Acrodermatitis 35 0.041
436
P IGN003 Iga Nephropathy 1 34 0.041
437
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.041
438
VLV036 Vulvar Disease 33 0.041
439
GND003 Gonadal Disease 32 0.041
440
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 31 0.041
441
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 30 0.041
442
c INH004 Inherited Blood Coagulation Disease 29 0.041
443
c PMP006 Pemphigus Vulgaris, Familial 26 0.041
444
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 25 0.041
445
EGS001 Egasyn 22 0.041
446
c ALZ012 Alzheimer Disease 12 20 0.041
447
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 20 0.041
448
DSS003 Disseminated Eosinophilic Collagen Disease 20 0.041
449
SCL001 Scalp Dermatosis 18 0.041
450
c RSM003 Rasmussen Subacute Encephalitis 17 0.041
451
P LNG032 Lung Cancer 99 0.034
452
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.034
453
P OVR042 Ovarian Cancer 82 0.034
454
P PLM037 Pulmonary Hypertension 79 0.034
455
P FNC027 Fanconi Anemia, Complementation Group a 78 0.034
456
ANX010 Anxiety 72 0.034
457
EWN003 Ewing Sarcoma 72 0.034
458
SVR004 Severe Combined Immunodeficiency 71 0.034
459
P RSP003 Respiratory Failure 71 0.034
460
BRC012 Brucellosis 71 0.034
461
DWN001 Down Syndrome 70 0.034
462
P TST021 Testicular Germ Cell Tumor 70 0.034
463
ALL003 Allergic Rhinitis 68 0.034
464
P DYS007 Dyskeratosis Congenita 68 0.034
465
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.034
466
c SML038 Small Cell Cancer of the Lung 67 0.034
467
BRS051 Breast Disease 67 0.034
468
c BSL007 Basal Cell Carcinoma 66 0.034
469
P ASP006 Aspergillosis 65 0.034
470
P THY023 Thymoma 65 0.034
471
P PNC044 Pancreatitis 64 0.034
472
CMB081 Combined Immunodeficiency, X-Linked 64 0.034
473
MST017 Mast Cell Disease 63 0.034
474
P LNG028 Long Qt Syndrome 63 0.034
475
MTR014 Motor Neuron Disease 62 0.034
476
P CMR001 Camurati-Engelmann Disease 62 0.034
477
P RHN004 Rhinitis 62 0.034
478
P MTR004 Maturity-Onset Diabetes of the Young 62 0.034
479
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.034
480
P RHB003 Rhabdomyosarcoma 61 0.034
481
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 59 0.034
482
PNC034 Pancreas Disease 59 0.034
483
P PLY019 Polyneuropathy 58 0.034
484
P SML001 Small Cell Carcinoma 58 0.034
485
P LTR001 Lateral Sclerosis 58 0.034
486
DMY004 Demyelinating Disease 58 0.034
487
RNL065 Renal Cell Carcinoma, Papillary, 1 56 0.034
488
HYP060 Hyperinsulinism 56 0.034
489
LYM027 Lymphopenia 56 0.034
490
P ACT008 Actinic Keratosis 56 0.034
491
P PRM006 Primary Biliary Cirrhosis 55 0.034
492
SPP010 Suppressor of Tumorigenicity 3 55 0.034
493
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 54 0.034
494
P ICH004 Ichthyosis 54 0.034
495
c INT064 Intermediate Uveitis 54 0.034
496
TST014 Testicular Cancer 54 0.034
497
c OVR114 Ovarian Cancer 1 54 0.034
498
P FNC004 Fanconi Syndrome 54 0.034
499
IMP005 Impotence 54 0.034
500
PRP080 Peripheral Artery Disease 54 0.034
501
SPN041 Spinal Cord Disease 54 0.034
502
CLL003 Cellulitis 53 0.034
503
P PLY023 Polycystic Liver Disease 53 0.034
504
DSM007 Desmoplastic Small Round Cell Tumor 53 0.034
505
ALC009 Alcoholic Liver Cirrhosis 53 0.034
506
c TCL005 T-Cell Prolymphocytic Leukemia 53 0.034
507
GGR001 Geographic Tongue 52 0.034
508
P SHR001 Short Bowel Syndrome 52 0.034
509
CLC006 Calcinosis 51 0.034
510
RFL001 Reflex Sympathetic Dystrophy 51 0.034
511
MYL003 Myeloid Sarcoma 51 0.034
512
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 51 0.034
513
c INV001 Invasive Aspergillosis 51 0.034
514
CRN027 Corneal Neovascularization 51 0.034
515
FBR086 Fibrolamellar Carcinoma 50 0.034
516
P LPM005 Lipomatosis 50 0.034
517
OPS006 Opsoclonus-Myoclonus Syndrome 50 0.034
518
MGC001 Megacolon 50 0.034
519
ECZ002 Eczema Herpeticum 49 0.034
520
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.034
521
SNS003 Sensory Peripheral Neuropathy 48 0.034
522
c ACT020 Acute T Cell Leukemia 48 0.034
523
ISC002 Ischemic Optic Neuropathy 48 0.034
524
PLC008 Placenta Disease 48 0.034
525
c CHR418 Chronic Leukemia 46 0.034
526
ANT039 Antisynthetase Syndrome 46 0.034
527
PMP004 Pemphigus Foliaceus 46 0.034
528
ATN004 Autonomic Neuropathy 46 0.034
529
OVR094 Ovarian Epithelial Cancer 46 0.034
530
IRR003 Irritant Dermatitis 45 0.034
531
BLS007 Blastic Plasmacytoid Dendritic Cell 45 0.034
532
EXC002 Exocrine Pancreatic Insufficiency 45 0.034
533
SXL003 Sexual Disorder 45 0.034
534
P BCL005 B Cell Prolymphocytic Leukemia 44 0.034
535
c PSR021 Psoriasis 14, Pustular 44 0.034
536
P TST026 Testicular Germ Cell Cancer 44 0.034
537
BLP005 Blepharitis 43 0.034
538
TST015 Testicular Disease 43 0.034
539
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 43 0.034
540
c CHR579 Chiari Malformation Type Ii 42 0.034
541
OVR112 Ovarian Germ Cell Cancer 42 0.034
542
P RNL045 Renal Tubular Acidosis, Distal 42 0.034
543
LMB024 Limbic Encephalitis 42 0.034
544
c NNN010 Noonan Syndrome 3 42 0.034
545
ACN019 Acanthamoeba Keratitis 41 0.034
546
DND018 Dendritic Cell Tumor 41 0.034
547
GNT050 Genitourinary Tract Anomalies 41 0.034
548
MYC033 Myoclonus 40 0.034
549
P PST059 Pustular Psoriasis 40 0.034
550
ALP097 Alopecia Universalis Congenita 40 0.034
551
c NPH049 Nephrotic Syndrome, Type 2 40 0.034
552
P CRB059 Cerebellar Degeneration 40 0.034
553
c NNN012 Noonan Syndrome 5 39 0.034
554
ALG001 Algoneurodystrophy 39 0.034
555
PRR013 Prurigo Nodularis 39 0.034
556
EYL005 Eyelid Disease 39 0.034
557
GST010 Gestational Trophoblastic Neoplasm 38 0.034
558
VLV008 Vulvitis 38 0.034
559
PPL019 Papillary Conjunctivitis 38 0.034
560
CND006 Candida Glabrata 38 0.034
561
TRP005 Trophoblastic Neoplasm 37 0.034
562
c SBC035 Subacute Cutaneous Lupus Erythematosus 37 0.034
563
SXD001 Sex Differentiation Disease 37 0.034
564
P GRM010 Germ Cells Tumors 37 0.034
565
HMR023 Hemorrhagic Cystitis 36 0.034
566
P CNN004 Connective Tissue Cancer 35 0.034
567
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.034
568
PRN039 Paraneoplastic Syndromes 35 0.034
569
ACT003 Acute Kidney Tubular Necrosis 34 0.034
570
c THY107 Thymoma, Familial 34 0.034
571
PRN032 Paraneoplastic Cerebellar Degeneration 33 0.034
572
AKN002 Akinetic Mutism 33 0.034
573
LCH003 Lichen Nitidus 33 0.034
574
OCC001 Occupational Dermatitis 32 0.034
575
RDT001 Radiation Cystitis 32 0.034
576
VSC012 Vesiculobullous Skin Disease 32 0.034
577
PMP009 Pemphigus Erythematosus 31 0.034
578
GST059 Gestational Trophoblastic Tumor 30 0.034
579
c NRM008 Neuromyelitis Optica Spectrum Disorder 30 0.034
580
MST020 Mast Cell Activation Syndrome 30 0.034
581
P SCK034 Sickle Beta Thalassemia 29 0.034
582
URN022 Urinary Tract Infections, Recurrent 29 0.034
583
c ALP039 Alopecia Areata 1 27 0.034
584
PTY004 Pityriasis Lichenoides 26 0.034
585
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 24 0.034
586
PRN033 Paraneoplastic Neurologic Disorders 23 0.034
587
MLL009 Mullerian Aplasia 21 0.034
588
PHL001 Phlyctenulosis 19 0.034
589
CHR176 Chromophil Renal Cell Carcinoma 19 0.034
590
ICH018 Ichthyosis Linearis Circumflexa 16 0.034
591
NNH003 Non-Hodgkin Lymphoma, Childhood 14 0.034
592
GRN045 Granulosis Rubra Nasi 14 0.034
593
MYC032 Myoclonic Encephalopathy of Infants 13 0.034
594
P DLT002 Dilated Cardiomyopathy 76 0.024
595
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.024
596
MSC157 Muscular Dystrophy, Duchenne Type 74 0.024
597
PSY004 Psychotic Disorder 72 0.024
598
THY028 Thyroid Cancer 72 0.024
599
P FML011 Familial Adenomatous Polyposis 71 0.024
600
P SCH015 Schizophrenia 71 0.024
601
P HRP006 Herpes Simplex 70 0.024
602
P NRF023 Neurofibromatosis, Type Ii 69 0.024
603
P TBR001 Tuberous Sclerosis 69 0.024
604
P PLM036 Pulmonary Fibrosis 68 0.024
605
OMN001 Omenn Syndrome 68 0.024
606
P MCL013 Mucolipidosis Iv 67 0.024
607
P MSC005 Muscular Dystrophy 66 0.024
608
MXD005 Mixed Connective Tissue Disease 66 0.024
609
P CLC063 Celiac Disease 1 65 0.024
610
NRF007 Neurofibroma 65 0.024
611
P HYP061 Hypertrophic Cardiomyopathy 65 0.024
612
RCT015 Reactive Arthritis 65 0.024
613
INC002 Inclusion Body Myositis 64 0.024
614
NRL005 Neurilemmoma 64 0.024
615
c ACT075 Acute Myocardial Infarction 64 0.024
616
SVR097 Severe Cutaneous Adverse Reaction 64 0.024
617
MSC152 Muscular Dystrophy, Becker Type 64 0.024
618
P INT143 Interstitial Cystitis 63 0.024
619
c ACT210 Acute Respiratory Distress Syndrome 63 0.024
620
c TBR025 Tuberous Sclerosis 1 63 0.024
621
CRD119 Cardiac Arrest 63 0.024
622
P HRM001 Hermansky-Pudlak Syndrome 62 0.024
623
P CRG003 Crigler-Najjar Syndrome, Type I 62 0.024
624
P HYP086 Hypothyroidism 62 0.024
625
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.024
626
c ACT027 Acute Pancreatitis 61 0.024
627
NRV006 Nervous System Cancer 61 0.024
628
STF001 Stiff-Person Syndrome 61 0.024
629
P FBR017 Fibrosarcoma 61 0.024
630
P GST044 Gastritis 61 0.024
631
CNG008 Congenital Ichthyosiform Erythroderma 61 0.024
632
HRP004 Herpes Zoster 61 0.024
633
P BPL003 Bipolar Disorder 61 0.024
634
CHL068 Cholestasis 60 0.024
635
c CHL119 Cholangitis, Primary Sclerosing 60 0.024
636
c VRL010 Viral Hepatitis 59 0.024
637
PST028 Post-Traumatic Stress Disorder 59 0.024
638
PRS047 Prostatitis 59 0.024
639
MLG077 Malignant Peripheral Nerve Sheath Tumor 59 0.024
640
P EPD009 Epidermolysis Bullosa Dystrophica 59 0.024
641
MRT001 Muir-Torre Syndrome 59 0.024
642
TRN015 Transient Cerebral Ischemia 58 0.024
643
P HYP069 Hyperparathyroidism 58 0.024
644
P MYC008 Myocarditis 58 0.024
645
NRN004 Neuroendocrine Tumor 58 0.024
646
OCL020 Ocular Cicatricial Pemphigoid 58 0.024
647
P OCL002 Oculocutaneous Albinism 57 0.024
648
WLL006 Wells Syndrome 57 0.024
649
c CRP023 Carpenter Syndrome 1 57 0.024
650
CHR003 Cherubism 57 0.024
651
CHL014 Cholera 56 0.024
652
P MGR003 Migraine with Aura 56 0.024
653
BLD044 Bladder Disease 55 0.024
654
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 55 0.024
655
MGR028 Migraine with or Without Aura 1 55 0.024
656
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 55 0.024
657
CPR004 Coproporphyria, Hereditary 54 0.024
658
TRM010 Traumatic Brain Injury 54 0.024
659
HDR002 Hidradenitis Suppurativa 54 0.024
660
RST001 Restless Legs Syndrome 54 0.024
661
OPT009 Optic Neuritis 53 0.024
662
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.024
663
P VNS003 Venous Insufficiency 53 0.024
664
PRP021 Peripheral Nervous System Neoplasm 53 0.024
665
HPT009 Hepatopulmonary Syndrome 53 0.024
666
c ANT034 Anterior Uveitis 53 0.024
667
P SCL009 Sclerosing Cholangitis 53 0.024
668
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 53 0.024
669
P HRD018 Hair Disease 53 0.024
670
P PNV001 Panuveitis 52 0.024
671
c PNS012 Paine Syndrome 52 0.024
672
LNT004 Lentigines 52 0.024
673
URM002 Uremia 52 0.024
674
c HPT015 Hepatitis D 52 0.024
675
P CHL066 Cholangitis 52 0.024
676
RTN023 Retinitis 52 0.024
677
PRN014 Paronychia 52 0.024
678
c ACT134 Acute Liver Failure 52 0.024
679
PLR008 Pleurisy 52 0.024
680
P PRC012 Pericardial Effusion 52 0.024
681
MMB001 Membranoproliferative Glomerulonephritis 51 0.024
682
MCL006 Macular Retinal Edema 51 0.024
683
CHR001 Churg-Strauss Syndrome 51 0.024
684
NRM004 Neuroma 51 0.024
685
THY030 Thyroid Gland Disease 51 0.024
686
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 51 0.024
687
P OPN001 Open-Angle Glaucoma 51 0.024
688
P LCT001 Lactic Acidosis 51 0.024
689
STR072 Stromal Keratitis 50 0.024
690
FCL012 Facial Paralysis 50 0.024
691
SCB001 Scabies 50 0.024
692
SPR010 Sporotrichosis 50 0.024
693
RTN003 Retinal Ischemia 50 0.024
694
c RTN162 Retinitis Pigmentosa 2 50 0.024
695
P SCL015 Scleritis 50 0.024
696
GNG005 Gangliocytoma 50 0.024
697
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.024
698
P PRK001 Porokeratosis 49 0.024
699
MTB004 Metabolic Acidosis 49 0.024
700
DRM011 Dermatophytosis 48 0.024
701
FSC004 Fasciitis 48 0.024
702
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.024
703
P HYP087 Hypotrichosis 48 0.024
704
PRS012 Pars Planitis 48 0.024
705
P CRN028 Corneal Ulcer 48 0.024
706
P SDR002 Siderosis 48 0.024
707
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 47 0.024
708
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.024
709
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.024
710
MLT016 Multicentric Reticulohistiocytosis 47 0.024
711
HDR003 Hidradenitis 47 0.024
712
GYN001 Gynecomastia 47 0.024
713
c CHR431 Chronic Venous Insufficiency 47 0.024
714
VLV032 Vulva Cancer 47 0.024
715
P ATX024 Ataxia-Oculomotor Apraxia 3 47 0.024
716
P DMY001 Demyelinating Polyneuropathy 46 0.024
717
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.024
718
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.024
719
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.024
720
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 46 0.024
721
EPD070 Epidermoid Cysts 46 0.024
722
DDN006 Duodenitis 46 0.024
723
THR035 Thrombasthenia 46 0.024
724
CNT025 Central Pontine Myelinolysis 45 0.024
725
ALB002 Albinism 45 0.024
726
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.024
727
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.024
728
CRD001 Cardiac Tamponade 45 0.024
729
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.024
730
PRN049 Paraneoplastic Pemphigus 45 0.024
731
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.024
732
SPC005 Speech Disorder 44 0.024
733
STR089 Storage Pool Platelet Disease 43 0.024
734
ACT058 Active Peptic Ulcer Disease 43 0.024
735
NCR004 Nocardiosis 43 0.024
736
NRN002 Neuronitis 43 0.024
737
LCH001 Leech Infestation 43 0.024
738
URM005 Uremic Pruritus 43 0.024
739
NRF003 Neurofibrosarcoma 42 0.024
740
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.024
741
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.024
742
PCH007 Pouchitis 42 0.024
743
CLP006 Clopidogrel Resistance 42 0.024
744
HYP026 Hypoglycemic Coma 41 0.024
745
BLN002 Balanitis Xerotica Obliterans 41 0.024
746
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 41 0.024
747
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.024
748
SPR066 Superficial Siderosis 40 0.024
749
GNT006 Giant Papillary Conjunctivitis 40 0.024
750
AYM001 Ayme-Gripp Syndrome 40 0.024
751
PRT019 Protein-Losing Enteropathy 40 0.024
752
DRM009 Dermatomycosis 39 0.024
753
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.024
754
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.024
755
AMN002 Amino Acid Metabolic Disorder 38 0.024
756
EPD022 Epidermolysis Bullosa Pruriginosa 38 0.024
757
DYS016 Dysgammaglobulinemia 38 0.024
758
LYM005 Lymphocele 37 0.024
759
ABD010 Abdominal Wall Defect 37 0.024
760
PTY002 Pityriasis Versicolor 36 0.024
761
ENG004 Engraftment Syndrome 36 0.024
762
INT003 Intracranial Hypotension 36 0.024
763
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.024
764
c DRM054 Dermatitis, Atopic, 2 35 0.024
765
TXC001 Toxic Megacolon 34 0.024
766
SPR034 Superior Limbic Keratoconjunctivitis 34 0.024
767
HMP001 Hemopericardium 34 0.024
768
FLL019 Follicular Mucinosis 34 0.024
769
RHM013 Rheumatoid Nodulosis 33 0.024
770
STY001 Satoyoshi Syndrome 32 0.024
771
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.024
772
ALP048 Alopecia Totalis 31 0.024
773
ATM052 Autoimmune Disease 1 30 0.024
774
INT065 Interstitial Keratitis 29 0.024
775
SPN340 Spontaneous Intracranial Hypotension 28 0.024
776
P MRL001 Meralgia Paresthetica 28 0.024
777
QNQ001 Quinquaud's Decalvans Folliculitis 28 0.024
778
EXF003 Exfoliative Dermatitis 28 0.024
779
CVR002 Cavernous Sinus Thrombosis 28 0.024
780
RVR002 Reversible Cerebral Vasoconstriction Syndrome 27 0.024
781
LNR004 Linear Porokeratosis 27 0.024
782
c WSK002 Wiskott-Aldrich Syndrome 2 27 0.024
783
CHL075 Cheilitis Glandularis 26 0.024
784
INF057 Inflammatory Linear Verrucous Epidermal Nevus 25 0.024
785
DFF031 Diffuse Alveolar Hemorrhage 25 0.024
786
INF021 Infant Gynecomastia 25 0.024
787
c HYP699 Hyperekplexia 1 25 0.024
788
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.024
789
P PPL026 Papular Mucinosis 23 0.024
790
UVL003 Uveal Diseases 23 0.024
791
P C1Q005 C1q Nephropathy 23 0.024
792
LKP001 Leukoplakia of Penis 23 0.024
793
SKN010 Skin Epithelioid Hemangioma 22 0.024
794
LPS019 Lupus Erythematosus Tumidus 22 0.024
795
FCL001 Facial Dermatosis 21 0.024
796
CYT017 Cytophagic Histiocytic Panniculitis 21 0.024
797
SPR019 Superficial Keratitis 20 0.024
798
NTL003 Notalgia Paresthetica 20 0.024
799
PPL027 Papular Urticaria 20 0.024
800
PTY005 Pityriasis Lichenoides Chronica 19 0.024
801
PST047 Post-Traumatic Epilepsy 19 0.024
802
LNR010 Linear Lichen Planus 19 0.024
803
LPS018 Lupus Erythematosus Panniculitis 19 0.024
804
INB001 Inborn Amino Acid Metabolism Disorder 16 0.024
805
DPD001 Deep Dermatophytosis 16 0.024
806
GRN021 Granulomatous Rosacea 16 0.024
807
AMN012 Aminoacidopathies 15 0.024
808
ACR080 Acral Persistent Papular Mucinosis 12 0.024
809
ATR076 Atrophic Muscular Disease 6 0.024
Content
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