Search results for [Pyr1]-Apelin-13

21322 hits were found for [Pyr1]-Apelin-13

# Family MCID Name MIFTS Score
1
P HPT023 Hepatocellular Carcinoma 100 1.000
2
P CLR023 Colorectal Cancer 99 1.000
3
P LNG032 Lung Cancer 98 1.000
4
P PRS040 Prostate Cancer 97 1.000
5
P BRS047 Breast Cancer 97 1.000
6
ESP021 Esophageal Cancer 90 1.000
7
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.000
8
c AMY091 Amyotrophic Lateral Sclerosis 1 89 1.000
9
P OVR042 Ovarian Cancer 88 1.000
10
P ALZ034 Alzheimer Disease 88 1.000
11
c SYS001 Systemic Lupus Erythematosus 86 1.000
12
MYL069 Myeloma, Multiple 85 1.000
14
c LKM061 Leukemia, Acute Myeloid 84 1.000
15
P PNC035 Pancreatic Cancer 84 1.000
16
P GST053 Gastric Cancer 83 1.000
17
NRL016 Neural Tube Defects 82 1.000
18
P ATX030 Ataxia-Telangiectasia 82 1.000
19
c FNC027 Fanconi Anemia, Complementation Group a 81 1.000
20
MLR004 Malaria 81 1.000
21
CYS001 Cystic Fibrosis 81 1.000
22
P GLM040 Glioma Susceptibility 1 81 1.000
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 1.000
24
STR067 Stroke, Ischemic 81 1.000
25
P RTT002 Rett Syndrome 80 1.000
26
P RHM011 Rheumatoid Arthritis 80 1.000
27
SQM013 Squamous Cell Carcinoma, Head and Neck 80 1.000
28
c NRF023 Neurofibromatosis, Type Ii 80 1.000
29
P BLD134 Bladder Cancer 79 1.000
30
c DLT002 Dilated Cardiomyopathy 79 1.000
31
P RTN008 Retinitis Pigmentosa 79 1.000
32
P LKM071 Leukemia, Chronic Lymphocytic 79 1.000
33
PFF001 Pfeiffer Syndrome 79 1.000
34
CNN003 Conn's Syndrome 79 1.000
35
INS024 Insulin-Like Growth Factor I 79 1.000
36
c CWD006 Cowden Syndrome 1 78 1.000
37
GST019 Gastrointestinal Stromal Tumor 78 1.000
38
RNL114 Renal Cell Carcinoma, Nonpapillary 78 1.000
39
OST012 Osteoarthritis 78 1.000
40
P PRK057 Parkinson Disease, Late-Onset 78 1.000
41
P LYN001 Lynch Syndrome 77 1.000
42
P MDL005 Medulloblastoma 77 1.000
43
MRF001 Marfan Syndrome 77 1.000
44
c TBR025 Tuberous Sclerosis 1 77 1.000
45
PLM134 Pulmonary Fibrosis, Idiopathic 77 1.000
46
c NRF024 Neurofibromatosis, Type I 77 1.000
47
AST005 Asthma 76 1.000
48
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.000
49
CRV035 Cervical Cancer 76 1.000
50
P NNN008 Noonan Syndrome 1 76 1.000
51
KPS004 Kaposi Sarcoma 75 1.000
52
P HRT032 Heart Disease 75 1.000
53
PHN003 Phenylketonuria 75 1.000
54
GLB015 Glioblastoma Multiforme 75 1.000
55
c ATR087 Atrial Standstill 1 75 1.000
56
c ART115 Aortic Valve Disease 1 75 1.000
57
ADR007 Adrenoleukodystrophy 75 1.000
58
P APL001 Aplastic Anemia 74 1.000
59
BRN028 Brain Cancer 74 1.000
60
END057 Endometrial Cancer 74 1.000
61
SCK003 Sickle Cell Anemia 74 1.000
62
LPT014 Leptin Deficiency or Dysfunction 74 1.000
63
P SCH015 Schizophrenia 74 1.000
64
c HMC039 Hemochromatosis, Type 1 74 1.000
65
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 1.000
66
c BTT014 Beta-Thalassemia 74 1.000
67
c MNN043 Meningioma, Familial 74 1.000
68
CRH001 Crohn's Disease 74 1.000
69
P NJM001 Nijmegen Breakage Syndrome 74 1.000
70
VNH007 Von Hippel-Lindau Syndrome 73 1.000
71
SVR004 Severe Combined Immunodeficiency 73 1.000
72
c HYP836 Hypercholesterolemia, Familial, 1 73 1.000
73
ULC004 Ulcerative Colitis 73 1.000
74
PLM129 Pulmonary Disease, Chronic Obstructive 73 1.000
75
c SPN225 Spondyloarthropathy 1 73 1.000
76
RNL065 Renal Cell Carcinoma, Papillary, 1 73 1.000
77
c THR092 Thrombophilia Due to Thrombin Defect 73 1.000
78
BSL036 Basal Cell Nevus Syndrome 73 1.000
79
P CNR004 Cone-Rod Dystrophy 2 73 1.000
80
P FML018 Familial Mediterranean Fever 73 1.000
81
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.000
82
P RTN024 Retinoblastoma 73 1.000
83
ANX010 Anxiety 73 1.000
84
P HYP724 Hyperlipoproteinemia, Type Iii 73 1.000
85
P ALG028 Alagille Syndrome 1 73 1.000
86
MSC157 Muscular Dystrophy, Duchenne Type 72 1.000
87
LYM143 Lymphoma, Non-Hodgkin, Familial 72 1.000
88
SCH036 Scheie Syndrome 72 1.000
89
BRT054 Brittle Bone Disorder 72 1.000
90
c MCP050 Mucopolysaccharidosis, Type Ii 72 1.000
91
c TBR026 Tuberous Sclerosis 2 72 1.000
92
P JBR020 Joubert Syndrome 1 72 1.000
93
P KDN018 Kidney Disease 72 1.000
94
P LFR001 Li-Fraumeni Syndrome 72 1.000
95
c HPT073 Hepatitis C Virus 72 1.000
96
P HNT016 Huntington Disease 72 1.000
97
c MLT156 Multiple Endocrine Neoplasia, Type I 72 1.000
98
P FML011 Familial Adenomatous Polyposis 72 1.000
99
P GRF003 Graft-Versus-Host Disease 72 1.000
100
OTT002 Otitis Media 72 1.000
101
FBR012 Fabry Disease 72 1.000
102
c LKM063 Leukemia, Chronic Myeloid 72 1.000
103
P WSK001 Wiskott-Aldrich Syndrome 72 1.000
104
AGM019 Agammaglobulinemia, X-Linked 71 1.000
105
P PHC003 Pheochromocytoma 71 1.000
106
ACR007 Acromegaly 71 1.000
107
HMN044 Human Immunodeficiency Virus Type 1 71 1.000
108
c EXD008 Exudative Vitreoretinopathy 1 71 1.000
109
WLS001 Wilson Disease 71 1.000
110
PRP027 Peripheral Vascular Disease 71 1.000
111
CNT097 Central Hypoventilation Syndrome, Congenital 71 1.000
112
P BRG001 Brugada Syndrome 71 1.000
113
BHC003 Behcet Syndrome 71 1.000
114
P EPL164 Epilepsy 71 1.000
115
P SRC025 Sarcoidosis 1 70 1.000
116
P ATS364 Autism 70 1.000
117
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 1.000
118
P MTC003 Metachromatic Leukodystrophy 70 1.000
119
DFC004 Deficiency Anemia 70 1.000
120
P AMY004 Amyloidosis 70 1.000
121
GST040 Gastric Adenocarcinoma 70 1.000
122
MYL009 Myelodysplastic Syndrome 70 1.000
123
MLT157 Multiple System Atrophy 1 70 1.000
124
DWN001 Down Syndrome 70 1.000
125
APR006 Apert Syndrome 70 1.000
126
c GLY008 Glycogen Storage Disease Ii 70 1.000
127
MYL005 Myelofibrosis 70 1.000
128
LGH007 Leigh Syndrome 70 1.000
129
c GCH015 Gaucher Disease, Type I 70 1.000
130
P CRD224 Cardiofaciocutaneous Syndrome 1 70 1.000
131
MCC012 Mccune-Albright Syndrome 70 1.000
132
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 1.000
133
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 1.000
134
ADN011 Adenoid Cystic Carcinoma 70 1.000
135
PTZ001 Peutz-Jeghers Syndrome 70 1.000
136
P OST001 Osteopetrosis 70 1.000
137
P HYP061 Hypertrophic Cardiomyopathy 70 1.000
138
P FRG001 Fragile X Syndrome 70 1.000
139
P TTR001 Tetralogy of Fallot 70 1.000
140
P MLN066 Melanoma, Cutaneous Malignant 1 70 1.000
141
c CHR684 Chronic Kidney Disease 70 1.000
142
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 1.000
143
SMT004 Smith-Lemli-Opitz Syndrome 70 1.000
144
ADL002 Adult Syndrome 70 1.000
145
c PNC108 Pancreatitis, Hereditary 70 1.000
146
P MYP004 Myopathy 70 1.000
147
CRT072 Creutzfeldt-Jakob Disease 70 1.000
148
P TBR001 Tuberous Sclerosis 70 1.000
149
CNG034 Congestive Heart Failure 69 1.000
150
P DMN001 Diamond-Blackfan Anemia 69 1.000
151
P ASP006 Aspergillosis 69 1.000
152
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.000
153
WRN001 Werner Syndrome 69 1.000
154
ABT001 Abetalipoproteinemia 69 1.000
155
P KRB001 Krabbe Disease 69 1.000
156
PLY001 Polycythemia Vera 69 1.000
157
PLM001 Pulmonary Tuberculosis 69 1.000
158
P RTH006 Rothmund-Thomson Syndrome, Type 2 69 1.000
159
P MLN008 Melanoma 69 1.000
160
P ART022 Arthritis 69 1.000
161
ACR008 Acrocallosal Syndrome 69 1.000
162
SVR097 Severe Cutaneous Adverse Reaction 69 1.000
163
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 1.000
164
P PRM011 Primary Ciliary Dyskinesia 69 1.000
165
CRB037 Cerebral Palsy 69 1.000
166
P SLP006 Sleep Apnea 69 1.000
167
P TYS001 Tay-Sachs Disease 69 1.000
168
LYM133 Lymphoma, Hodgkin, Classic 69 1.000
169
P OCL013 Oculodentodigital Dysplasia 69 1.000
170
P HYP086 Hypothyroidism 69 1.000
171
c PRG042 Progressive Familial Heart Block, Type Ia 69 1.000
172
P LPR021 Leprosy 3 69 1.000
173
ART016 Aortic Aneurysm 69 1.000
174
LKC009 Leukocyte Adhesion Deficiency, Type I 69 1.000
175
EWN003 Ewing Sarcoma 69 1.000
176
P MPL001 Maple Syrup Urine Disease 69 1.000
177
LYM007 Lymphangioleiomyomatosis 69 1.000
178
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 1.000
179
MST024 Mastocytosis, Cutaneous 69 1.000
180
P ANG001 Angelman Syndrome 69 1.000
181
P LKM062 Leukemia, Acute Lymphoblastic 69 1.000
182
MNT001 Mantle Cell Lymphoma 69 1.000
183
c MYT021 Myotonic Dystrophy 1 69 1.000
184
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.000
185
P LYM118 Lymphoma 68 1.000
186
NVS017 Nevus, Epidermal 68 1.000
187
ODN023 Odontochondrodysplasia 68 1.000
188
P CRN037 Craniosynostosis 68 1.000
189
P TMP003 Temporal Arteritis 68 1.000
190
P LVR013 Liver Disease 68 1.000
191
P PNM007 Pneumonia 68 1.000
192
P SYS005 Systemic Scleroderma 68 1.000
193
P MYC084 Mycobacterium Tuberculosis 1 68 1.000
194
CHL065 Cholangiocarcinoma 68 1.000
195
SND001 Sandhoff Disease 68 1.000
196
CMM004 Common Variable Immunodeficiency 68 1.000
197
c BSL007 Basal Cell Carcinoma 68 1.000
198
P LKM002 Leukemia 68 1.000
199
OBS002 Obsessive-Compulsive Disorder 68 1.000
200
CRZ001 Crouzon Syndrome 68 1.000
201
CST001 Costello Syndrome 68 1.000
202
SKN019 Skin Melanoma 68 1.000
203
PCK003 Pick Disease of Brain 68 1.000
204
c NMN015 Niemann-Pick Disease, Type C1 68 1.000
205
P MYS003 Myasthenia Gravis 68 1.000
206
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 1.000
207
P INF038 Influenza 68 1.000
208
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 1.000
209
P ESS003 Essential Thrombocythemia 68 1.000
210
BRN024 Bronchitis 68 1.000
211
c HMP004 Hemophilia B 68 1.000
212
CNN005 Connective Tissue Disease 68 1.000
213
P ALP004 Alport Syndrome 68 1.000
214
c CNG411 Congenital Disorder of Glycosylation, Type in 68 1.000
215
RCK004 Rickets 68 1.000
216
P MJR001 Major Depressive Disorder 68 1.000
217
MLD001 Melioidosis 68 1.000
218
P JVN014 Juvenile Polyposis Syndrome 68 1.000
219
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 1.000
220
P FRN006 Frontotemporal Dementia 68 1.000
221
PNC129 Pancreatic Adenocarcinoma 68 1.000
222
c MCL062 Mucolipidosis Ii Alpha/beta 68 1.000
223
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 1.000
224
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 1.000
225
c MCP052 Mucopolysaccharidosis, Type Vi 67 1.000
226
P KBK002 Kabuki Syndrome 1 67 1.000
227
P THR014 Thrombocytopenia 67 1.000
228
HYL004 Hyaline Fibromatosis Syndrome 67 1.000
229
P CWD010 Cowden Syndrome 67 1.000
230
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 1.000
231
GST092 Gastroesophageal Reflux 67 1.000
232
c HYP768 Hyperlipoproteinemia, Type I 67 1.000
233
P CRD119 Cardiac Arrest 67 1.000
234
P CRB048 Cerebral Cavernous Malformations 67 1.000
235
P HPT021 Hepatitis 67 1.000
236
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.000
237
P DYS007 Dyskeratosis Congenita 67 1.000
238
CHR103 Charge Syndrome 67 1.000
239
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 1.000
240
c INF071 Inflammatory Bowel Disease 1 67 1.000
241
FCT007 Factor Vii Deficiency 67 1.000
242
P HLP001 Holoprosencephaly 67 1.000
243
P OLG002 Oligodendroglioma 67 1.000
244
BLM001 Bloom Syndrome 67 1.000
245
c JVN004 Juvenile Myelomonocytic Leukemia 67 1.000
246
BRK010 Burkitt Lymphoma 67 1.000
247
CRB039 Cerebrovascular Disease 67 1.000
248
P FLL037 Follicular Lymphoma 67 1.000
249
ALL003 Allergic Rhinitis 67 1.000
250
c HMP029 Hemophilia a 67 1.000
251
OMN001 Omenn Syndrome 67 1.000
252
STH001 Saethre-Chotzen Syndrome 67 1.000
253
THY111 Thyroid Carcinoma, Familial Medullary 67 1.000
254
P SHW006 Shwachman-Diamond Syndrome 1 67 1.000
255
P CHR012 Chronic Granulomatous Disease 67 1.000
256
PSY004 Psychotic Disorder 67 1.000
257
P PRP003 Porphyria Cutanea Tarda 67 1.000
258
P TRN020 Turner Syndrome 67 1.000
259
FLL027 Fallopian Tube Carcinoma 67 1.000
260
P HYP098 Hypereosinophilic Syndrome 67 1.000
261
P BLD062 Bile Duct Cancer 67 1.000
262
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 1.000
263
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 1.000
264
c ATS007 Autism Spectrum Disorder 67 1.000
265
CRP001 Carpal Tunnel Syndrome 67 1.000
266
FBR011 Fibrodysplasia Ossificans Progressiva 67 1.000
267
P MLG056 Malignant Hyperthermia 67 1.000
268
c MGR028 Migraine with or Without Aura 1 67 1.000
269
PRT010 Parathyroid Carcinoma 67 1.000
270
c RHB024 Rhabdomyosarcoma 2 67 1.000
271
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 1.000
272
c PRM196 Premature Ovarian Failure 1 67 1.000
273
THY121 Thyroid Gland Anaplastic Carcinoma 66 1.000
274
MYC006 Mycosis Fungoides 66 1.000
275
LPT001 Leptospirosis 66 1.000
276
c TYR012 Tyrosinemia, Type I 66 1.000
277
WLF001 Wolff-Parkinson-White Syndrome 66 1.000
278
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 66 1.000
279
P CLC063 Celiac Disease 1 66 1.000
280
P LNG028 Long Qt Syndrome 66 1.000
281
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 1.000
282
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 1.000
283
ALC007 Alcohol Dependence 66 1.000
284
OST159 Osteogenic Sarcoma 66 1.000
285
ANG054 Angina Pectoris 66 1.000
286
GLL008 Gilles De La Tourette Syndrome 66 1.000
287
CHD001 Chediak-Higashi Syndrome 66 1.000
288
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 66 1.000
289
P TRC072 Treacher Collins Syndrome 1 66 1.000
290
P DMN002 Dementia 66 1.000
291
c FML021 Familial Hypercholesterolemia 66 1.000
292
P MSC005 Muscular Dystrophy 66 1.000
293
GLN010 Glanzmann Thrombasthenia 66 1.000
294
P SKN015 Skin Carcinoma 66 1.000
295
GRG001 Greig Cephalopolysyndactyly Syndrome 66 1.000
296
P NSP012 Nasopharyngeal Carcinoma 66 1.000
297
P CNG001 Congenital Myasthenic Syndrome 66 1.000
298
MYX005 Myxoid Liposarcoma 66 1.000
299
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 1.000
300
c PSD108 Pseudohypoparathyroidism, Type Ia 66 1.000
301
ART001 Arterial Tortuosity Syndrome 66 1.000
302
c FML346 Familial Adenomatous Polyposis 1 66 1.000
303
FCL009 Focal Dermal Hypoplasia 66 1.000
304
ADR054 Adrenocortical Carcinoma, Hereditary 66 1.000
305
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 1.000
306
P EPD009 Epidermolysis Bullosa Dystrophica 66 1.000
307
ACH004 Achondroplasia 66 1.000
308
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.000
309
LBR036 Leber Plus Disease 66 1.000
312
HYP056 Hypoglycemia 66 1.000
313
c HRD010 Hereditary Spastic Paraplegia 66 1.000
314
AND002 Androgen Insensitivity Syndrome 66 1.000
315
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 1.000
316
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 66 1.000
317
c LNG044 Long Qt Syndrome 1 66 1.000
318
P ATR011 Atrial Fibrillation 66 1.000
319
CHG001 Chagas Disease 66 1.000
320
P HYD006 Hydrocephalus 66 1.000
321
P MNN013 Meningitis 66 1.000
322
P DRM053 Dermatitis, Atopic 66 1.000
323
P CCK001 Cockayne Syndrome 66 1.000
324
LNG039 Lung Squamous Cell Carcinoma 66 1.000
325
MYL031 Myeloproliferative Neoplasm 66 1.000
326
MVL001 Mevalonic Aciduria 66 1.000
327
P NRV007 Nervous System Disease 66 1.000
328
c MCL013 Mucolipidosis Iv 66 1.000
329
SVR066 Severe Combined Immunodeficiency, X-Linked 66 1.000
330
P BRD002 Bardet-Biedl Syndrome 66 1.000
331
c SML038 Small Cell Cancer of the Lung 65 1.000
332
KHL003 Kohlschutter-Tonz Syndrome 65 1.000
333
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 1.000
334
CRN036 Craniopharyngioma 65 1.000
335
CNC002 Cinca Syndrome 65 1.000
336
P PLM036 Pulmonary Fibrosis 65 1.000
337
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.000
338
GTL001 Gitelman Syndrome 65 1.000
339
TTN003 Tetanus 65 1.000
340
c FML001 Familial Atrial Fibrillation 65 1.000
341
P LYS001 Loeys-Dietz Syndrome 65 1.000
342
P HRS035 Hirschsprung Disease 1 65 1.000
343
P ART005 Arteriovenous Malformation 65 1.000
344
LWC002 Lowe Oculocerebrorenal Syndrome 65 1.000
345
P AGM001 Agammaglobulinemia 65 1.000
346
P CNJ013 Conjunctivitis 65 1.000
347
P MCK013 Meckel Syndrome, Type 1 65 1.000
348
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 1.000
349
P DYS154 Dystonia 65 1.000
350
DMN031 Dementia, Lewy Body 65 1.000
351
KRT019 Keratitis, Hereditary 65 1.000
352
ACR006 Aceruloplasminemia 65 1.000
353
SRC014 Sarcoma 65 1.000
354
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 1.000
355
PPL049 Papillon-Lefevre Syndrome 65 1.000
356
P VNW001 Von Willebrand's Disease 65 1.000
357
P LPS002 Liposarcoma 65 1.000
358
P MTR004 Maturity-Onset Diabetes of the Young 65 1.000
359
P PSD087 Pseudoxanthoma Elasticum 65 1.000
360
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 1.000
361
AFB002 Afibrinogenemia, Congenital 65 1.000
362
P MTR014 Motor Neuron Disease 65 1.000
363
PRP001 Propionic Acidemia 65 1.000
364
TNG002 Tangier Disease 65 1.000
365
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 1.000
366
MSM014 Mismatch Repair Cancer Syndrome 65 1.000
367
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 1.000
368
BRR014 Barrett Esophagus 65 1.000
369
P CLD001 Cleidocranial Dysplasia 65 1.000
370
PND002 Pendred Syndrome 65 1.000
371
c ART101 Aortic Valve Disease 2 65 1.000
372
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 1.000
373
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 1.000
374
HRL003 Hurler Syndrome 65 1.000
375
IRR002 Irritable Bowel Syndrome 65 1.000
376
DRM014 Dermatofibrosarcoma Protuberans 65 1.000
377
P HRP006 Herpes Simplex 65 1.000
378
CHY002 Chylomicron Retention Disease 65 1.000
379
GRN037 Granulomatosis with Polyangiitis 65 1.000
380
MRK001 Merkel Cell Carcinoma 65 1.000
381
ATH013 Atherosclerosis Susceptibility 65 1.000
382
c WLM013 Wilms Tumor 1 65 1.000
383
P PLR004 Pleuropulmonary Blastoma 65 1.000
384
P CTS001 Cutis Laxa 65 1.000
385
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 1.000
386
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.000
387
P PRS038 Personality Disorder 65 1.000
388
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 65 1.000
389
KWS002 Kawasaki Disease 65 1.000
390
c DBT099 Diabetes Mellitus, Type I 65 1.000
391
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 1.000
392
MCK007 Muckle-Wells Syndrome 65 1.000
393
P ADL010 Adult Respiratory Distress Syndrome 65 1.000
394
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 1.000
395
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 1.000
396
CLN015 Colon Adenocarcinoma 65 1.000
397
CRB011 Cerebrotendinous Xanthomatosis 65 1.000
398
P THY023 Thymoma 65 1.000
399
LYS012 Lysosomal Acid Lipase Deficiency 65 1.000
400
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.000
401
P CHR071 Charcot-Marie-Tooth Disease 65 1.000
402
c MCP001 Mucopolysaccharidosis Iii 65 1.000
403
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 1.000
404
PRT036 Peritonitis 64 1.000
405
MNK001 Menkes Disease 64 1.000
406
APN008 Apnea, Obstructive Sleep 64 1.000
407
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 1.000
408
ANG020 Angiosarcoma 64 1.000
409
NRM005 Neuromuscular Disease 64 1.000
410
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 1.000
411
PLL001 Pallister-Hall Syndrome 64 1.000
412
P NRN021 Neuronal Ceroid Lipofuscinosis 64 1.000
413
P HRM001 Hermansky-Pudlak Syndrome 64 1.000
414
MYC079 Myoclonic Epilepsy of Lafora 64 1.000
415
NRF007 Neurofibroma 64 1.000
416
OVR029 Ovarian Hyperstimulation Syndrome 64 1.000
417
P CMP005 Campomelic Dysplasia 64 1.000
418
NRR002 Norrie Disease 64 1.000
419
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 1.000
420
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 64 1.000
421
P PRT008 Proteus Syndrome 64 1.000
422
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 1.000
423
CLF027 Cleft Palate, Isolated 64 1.000
424
BRK001 Brooke-Spiegler Syndrome 64 1.000
425
P MST009 Mastocytosis 64 1.000
426
TBC004 Tobacco Addiction 64 1.000
427
CTR172 Citrullinemia, Classic 64 1.000
428
c JVN010 Juvenile Rheumatoid Arthritis 64 1.000
429
GT001 Gout 64 1.000
430
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 1.000
431
P GLC113 Galactosemia I 64 1.000
432
ALS001 Alstrom Syndrome 64 1.000
433
CLR108 Colorectal Adenoma 64 1.000
434
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 1.000
435
P FRD001 Friedreich Ataxia 64 1.000
436
BRC012 Brucellosis 64 1.000
437
ART002 Arts Syndrome 64 1.000
438
DGR001 Digeorge Syndrome 64 1.000
439
ALP103 Alpha-1-Antitrypsin Deficiency 64 1.000
440
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 1.000
441
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 1.000
442
P PLZ001 Pelizaeus-Merzbacher Disease 64 1.000
443
PRP083 Porphyria, Acute Intermittent 64 1.000
444
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 1.000
445
P PRD008 Periodontitis 64 1.000
446
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 1.000
447
c CNG006 Congenital Hypothyroidism 64 1.000
448
MSC007 Muscle Hypertrophy 64 1.000
449
PLM031 Poliomyelitis 64 1.000
450
P CRN015 Cornelia De Lange Syndrome 64 1.000
451
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 1.000
452
HJD001 Hajdu-Cheney Syndrome 64 1.000
453
SPT006 Septooptic Dysplasia 64 1.000
454
DSM004 Desmoid Tumor 64 1.000
455
c GST103 Gastric Cancer, Hereditary Diffuse 64 1.000
456
P FTL069 Fetal Akinesia Deformation Sequence 1 64 1.000
457
KND001 Kindler Syndrome 64 1.000
458
LYM017 Lyme Disease 64 1.000
459
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 1.000
460
RFS006 Refsum Disease, Classic 64 1.000
461
MGK001 Megakaryocytic Leukemia 64 1.000
462
RBR001 Roberts Syndrome 64 1.000
463
HYP020 Hyperprolactinemia 64 1.000
464
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 1.000
465
OST017 Osteomyelitis 64 1.000
466
P RHB003 Rhabdomyosarcoma 63 1.000
467
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 1.000
468
c MCP049 Mucopolysaccharidosis, Type Vii 63 1.000
469
c EPS035 Episodic Ataxia, Type 2 63 1.000
470
c DPH024 Diaphragmatic Hernia, Congenital 63 1.000
471
KRN002 Kearns-Sayre Syndrome 63 1.000
472
INC021 Incontinentia Pigmenti 63 1.000
473
LSH001 Leishmaniasis 63 1.000
474
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 1.000
475
BRT002 Birt-Hogg-Dube Syndrome 63 1.000
476
P ERL057 Early Infantile Epileptic Encephalopathy 63 1.000
477
P GLM045 Glioma 63 1.000
478
P GCH001 Gaucher's Disease 63 1.000
479
P HML002 Hemolytic Anemia 63 1.000
480
BLS001 Blau Syndrome 63 1.000
481
P NTR004 Neutropenia 63 1.000
482
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 1.000
483
P RNL100 Renal Hypodysplasia/aplasia 1 63 1.000
484
CYS013 Cystinuria 63 1.000
485
P ANR048 Aniridia 1 63 1.000
486
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 1.000
487
TYP007 Typhoid Fever 63 1.000
488
P VSC007 Vascular Disease 63 1.000
489
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 1.000
490
P HYP069 Hyperparathyroidism 63 1.000
491
PLG002 Plague 63 1.000
492
WLK001 Walker-Warburg Syndrome 63 1.000
493
c HYP794 Hyperoxaluria, Primary, Type I 63 1.000
494
CNT061 Conotruncal Heart Malformations 63 1.000
495
c MLG084 Malignant Fibrous Histiocytoma 63 1.000
496
P CRN300 Coronary Heart Disease 1 63 1.000
497
MSC152 Muscular Dystrophy, Becker Type 63 1.000
498
P DST002 Distal Arthrogryposis 63 1.000
499
P CRG003 Crigler-Najjar Syndrome, Type I 63 1.000
500
SKN016 Skin Disease 63 1.000
501
ACT119 Acute Promyelocytic Leukemia 63 1.000
502
P THR117 Three M Syndrome 1 63 1.000
503
P SHR029 Short Syndrome 63 1.000
504
INT146 Intervertebral Disc Disease 63 1.000
505
P HYP055 Hypoplastic Left Heart Syndrome 63 1.000
506
PTR032 Peters-Plus Syndrome 63 1.000
507
CHN016 Cohen Syndrome 63 1.000
508
P PTT014 Pitt-Hopkins Syndrome 63 1.000
509
END041 Endometrial Adenocarcinoma 63 1.000
510
CHR063 Chronic Mucocutaneous Candidiasis 63 1.000
511
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 1.000
512
c SYS004 Systemic Mastocytosis 63 1.000
513
HYP780 Hypoadrenocorticism, Familial 63 1.000
514
P MVM001 Movement Disease 63 1.000
515
HLT001 Holt-Oram Syndrome 63 1.000
516
c ACT068 Acute Cystitis 63 1.000
517
P CFF008 Coffin-Siris Syndrome 1 63 1.000
518
P LMY004 Leiomyosarcoma 63 1.000
519
c GLY060 Glycogen Storage Disease Ia 63 1.000
520
ANR007 Anorexia Nervosa 63 1.000
521
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 1.000
522
P END044 Endometriosis 63 1.000
523
RHB001 Rhabdoid Cancer 63 1.000
524
c ATM011 Autoimmune Hepatitis 63 1.000
525
BDD001 Budd-Chiari Syndrome 63 1.000
526
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 1.000
527
c OPT053 Optic Atrophy 1 63 1.000
528
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 1.000
529
c GLC092 Glaucoma, Primary Open Angle 62 1.000
530
c ALP101 Alpha-Thalassemia 62 1.000
531
INT323 Intraocular Pressure Quantitative Trait Locus 62 1.000
532
P ECT006 Ectodermal Dysplasia 62 1.000
533
CYC010 Cyclic Neutropenia 62 1.000
534
c LCL006 Localized Scleroderma 62 1.000
535
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.000
536
HMT002 Hematologic Cancer 62 1.000
537
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.000
538
ERL001 Early Myoclonic Encephalopathy 62 1.000
539
LPD008 Lipid Metabolism Disorder 62 1.000
540
LRN002 Laron Syndrome 62 1.000
541
ELL001 Ellis-Van Creveld Syndrome 62 1.000
542
CLT003 Colitis 62 1.000
543
c FNC043 Fanconi Anemia, Complementation Group E 62 1.000
544
c HPT001 Hepatitis C 62 1.000
545
NNN026 Noonan Syndrome with Multiple Lentigines 62 1.000
546
P PLY014 Polycystic Kidney Disease 62 1.000
547
P PSR002 Psoriasis 62 1.000
548
c GM1007 Gm1 Gangliosidosis 62 1.000
549
P EPL140 Epilepsy, Idiopathic Generalized 62 1.000
550
c HPT003 Hepatitis a 62 1.000
551
c GLY004 Glycogen Storage Disease V 62 1.000
552
P MCH002 Machado-Joseph Disease 62 1.000
553
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 1.000
554
c BRN108 Branchiootic Syndrome 1 62 1.000
555
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.000
556
DNH001 Donohue Syndrome 62 1.000
557
TKY002 Takayasu Arteritis 62 1.000
558
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 1.000
559
P SPN046 Spinal Muscular Atrophy 62 1.000
560
c SVR001 Severe Acute Respiratory Syndrome 62 1.000
561
LPP008 Lipoprotein Quantitative Trait Locus 62 1.000
562
PRM126 Primary Peritoneal Carcinoma 62 1.000
563
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 1.000
564
P HYP750 Hypertriglyceridemia, Familial 62 1.000
565
P EPL198 Epilepsy, Myoclonic Juvenile 62 1.000
566
c DYS056 Dystonia 12 62 1.000
567
c MLN065 Melanocytic Nevus Syndrome, Congenital 62 1.000
568
P LRS001 Larsen Syndrome 62 1.000
569
P DNT020 Dent Disease 1 62 1.000
570
P ESP024 Esophagitis 62 1.000
571
P TRC086 Trichohepatoenteric Syndrome 1 62 1.000
572
BLL006 Bullous Pemphigoid 62 1.000
573
P ART023 Arthropathy 62 1.000
574
c BRD010 Bardet-Biedl Syndrome 1 62 1.000
575
HYD038 Hydrops Fetalis, Nonimmune 62 1.000
576
CHR619 Chromosome 2q35 Duplication Syndrome 62 1.000
577
P VSC011 Vasculitis 62 1.000
578
P THN009 Thanatophoric Dysplasia, Type I 62 1.000
579
P BCK002 Beckwith-Wiedemann Syndrome 62 1.000
580
LSC001 Lesch-Nyhan Syndrome 62 1.000
581
P ORT004 Orthostatic Intolerance 62 1.000
582
c ANM038 Anemia, Autoimmune Hemolytic 62 1.000
583
PHL006 Phelan-Mcdermid Syndrome 62 1.000
584
c NMN013 Niemann-Pick Disease, Type a 62 1.000
585
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 1.000
586
ATM095 Autoimmune Disease 62 1.000
587
P ACR001 Aicardi-Goutieres Syndrome 62 1.000
588
ALL026 Allergic Hypersensitivity Disease 62 1.000
589
CRN239 Carnitine Deficiency, Systemic Primary 62 1.000
590
HYP810 Hypereosinophilic Syndrome, Idiopathic 62 1.000
591
P PRM002 Primary Hyperoxaluria 62 1.000
592
HSH003 Hashimoto Thyroiditis 62 1.000
593
BRS099 Breast Ductal Carcinoma 62 1.000
594
MNN042 Meningioma, Radiation-Induced 62 1.000
595
NRM019 Neuraminidase Deficiency 62 1.000
596
GLY010 Glycine Encephalopathy 62 1.000
597
CTN007 Cutaneous Leishmaniasis 62 1.000
598
CRC021 Carcinosarcoma 62 1.000
599
P CRN108 Cranioectodermal Dysplasia 1 62 1.000
600
TXC005 Toxic Shock Syndrome 62 1.000
601
P OST009 Osteochondritis Dissecans 62 1.000
602
P PRM006 Primary Biliary Cirrhosis 62 1.000
603
MSS001 Masa Syndrome 62 1.000
604
LVR012 Liver Cirrhosis 62 1.000
605
BLD131 Bladder Urothelial Carcinoma 62 1.000
606
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 62 1.000
607
ASP002 Aspartylglucosaminuria 62 1.000
608
MSL001 Measles 62 1.000
609
P PRP029 Porphyria 62 1.000
610
ESP020 Esophageal Atresia 62 1.000
611
P BTH005 Bethlem Myopathy 1 62 1.000
612
NTR005 Nutritional Deficiency Disease 62 1.000
613
P CRN038 Carney Complex Variant 61 1.000
614
ATY005 Atypical Teratoid Rhabdoid Tumor 61 1.000
615
CHL068 Cholestasis 61 1.000
616
NNL005 Non-Alcoholic Fatty Liver Disease 61 1.000
617
P DRM010 Dermatomyositis 61 1.000
618
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 1.000
619
PSR001 Psoriatic Arthritis 61 1.000
621
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 1.000
622
c MCP043 Mucopolysaccharidosis, Type Iiia 61 1.000
623
P INT143 Interstitial Cystitis 61 1.000
624
P KLL001 Kallmann Syndrome 61 1.000
625
NRM001 Neuromyelitis Optica 61 1.000
626
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 1.000
627
P HYP097 Hyperekplexia 61 1.000
628
MCK005 Mckusick-Kaufman Syndrome 61 1.000
629
HYP066 Hyperglycemia 61 1.000
630
OST003 Osteonecrosis 61 1.000
631
c PRX045 Peroxisome Biogenesis Disorder 1b 61 1.000
632
FTT001 Fatty Liver Disease 61 1.000
633
c MCP047 Mucopolysaccharidosis, Type Iva 61 1.000
634
CHN055 Chanarin-Dorfman Syndrome 61 1.000
635
INT002 Intermittent Claudication 61 1.000
636
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 1.000
637
P CHL002 Childhood Absence Epilepsy 61 1.000
638
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 1.000
639
DRM006 Dermatitis 61 1.000
640
CHR001 Churg-Strauss Syndrome 61 1.000
641
c PNS012 Paine Syndrome 61 1.000
642
c SCL052 Scleroderma, Familial Progressive 61 1.000
643
P THR005 Thrombotic Thrombocytopenic Purpura 61 1.000
644
P HYP035 Hypophosphatasia 61 1.000
645
WST001 West Syndrome 61 1.000
646
TMT001 Timothy Syndrome 61 1.000
647
P ENC018 Encephalopathy 61 1.000
648
YLL002 Yellow Fever 61 1.000
649
P ENC004 Encephalitis 61 1.000
650
ALC006 Alcoholic Hepatitis 61 1.000
651
CNV004 Canavan Disease 61 1.000
652
FCS002 Fucosidosis 61 1.000
653
CHR066 Chronic Fatigue Syndrome 61 1.000
654
OSS012 Osseous Heteroplasia, Progressive 61 1.000
655
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 61 1.000
656
WLD007 Waldenstroem's Macroglobulinemia 61 1.000
657
ALV005 Alveolar Soft Part Sarcoma 61 1.000
658
c WLM018 Wilms Tumor 5 61 1.000
659
ART141 Arteriovenous Malformations of the Brain 61 1.000
660
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 61 1.000
661
WHM001 Whim Syndrome 61 1.000
662
P ACH003 Achromatopsia 61 1.000
663
RCT015 Reactive Arthritis 61 1.000
664
P STS008 Sotos Syndrome 1 61 1.000
665
P PNC044 Pancreatitis 61 1.000
666
P SJG008 Sjogren Syndrome 61 1.000
667
GST033 Gestational Diabetes 61 1.000
668
ARG002 Argininosuccinic Aciduria 61 1.000
669
RTN017 Retinal Detachment 61 1.000
670
SDD001 Sudden Infant Death Syndrome 61 1.000
671
VRL011 Viral Infectious Disease 61 1.000
672
c PRT132 Protoporphyria, Erythropoietic, 1 61 1.000
673
FBR086 Fibrolamellar Carcinoma 61 1.000
674
APP008 Appendicitis 61 1.000
675
c ART144 Arthrogryposis, Distal, Type 1a 61 1.000
676
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 1.000
677
HYP052 Hyperkalemic Periodic Paralysis 61 1.000
678
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 1.000
679
P LPS004 Lupus Erythematosus 61 1.000
680
P HMN010 Hemangioma 61 1.000
681
DCB001 Decubitus Ulcer 61 1.000
682
LCR014 Lacrimoauriculodentodigital Syndrome 61 1.000
683
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 61 1.000
684
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 1.000
685
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 1.000
686
BTN003 Biotinidase Deficiency 60 1.000
687
NRL005 Neurilemmoma 60 1.000
688
P MYL006 Myeloid Leukemia 60 1.000
689
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 60 1.000
690
LGN002 Legionellosis 60 1.000
691
NTH001 Netherton Syndrome 60 1.000
692
NPH091 Nephrolithiasis, Calcium Oxalate 60 1.000
693
P KDN017 Kidney Cancer 60 1.000
694
SHG001 Shigellosis 60 1.000
695
HRP004 Herpes Zoster 60 1.000
696
TTH002 Tooth Agenesis 60 1.000
697
PTN001 Patent Foramen Ovale 60 1.000
698
P NPH012 Nephrotic Syndrome 60 1.000
699
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 60 1.000
700
PNM010 Pneumothorax, Primary Spontaneous 60 1.000
701
WLL001 Williams-Beuren Syndrome 60 1.000
702
SZR001 Sezary's Disease 60 1.000
703
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.000
704
RGH009 Right Atrial Isomerism 60 1.000
705
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 1.000
706
CFF002 Coffin-Lowry Syndrome 60 1.000
707
DRR016 Diarrhea 2, with Microvillus Atrophy 60 1.000
708
CNT105 Central Core Disease of Muscle 60 1.000
709
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 1.000
710
P TST021 Testicular Germ Cell Tumor 60 1.000
711
FND001 Fundus Albipunctatus 60 1.000
712
DPH001 Diphtheria 60 1.000
713
c LPM012 Lipomatosis, Multiple 60 1.000
714
c USH036 Usher Syndrome, Type I 60 1.000
715
TRG002 Trigeminal Neuralgia 60 1.000
716
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 1.000
717
c JVN061 Juvenile Arthritis 60 1.000
718
P SCL018 Scoliosis 60 1.000
719
P TXP001 Toxoplasmosis 60 1.000
720
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 1.000
721
P BNG030 Benign Ependymoma 60 1.000
722
OST024 Osteoporosis-Pseudoglioma Syndrome 60 1.000
723
INT066 Interstitial Lung Disease 60 1.000
724
P VNT002 Ventricular Septal Defect 60 1.000
725
c ACT027 Acute Pancreatitis 60 1.000
726
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 1.000
727
KFR001 Kufor-Rakeb Syndrome 60 1.000
728
HPT019 Hepatic Encephalopathy 60 1.000
729
THR100 Thrombocytopenic Purpura, Autoimmune 60 1.000
730
CRD223 Cardiac Arrhythmia 60 1.000
731
ACN002 Acanthosis Nigricans 60 1.000
732
HYP042 Hypochondroplasia 60 1.000
733
c EPS042 Episodic Ataxia, Type 1 60 1.000
734
ACQ007 Acquired Immunodeficiency Syndrome 60 1.000
735
LNG099 Lung Disease 60 1.000
736
c ORF037 Orofaciodigital Syndrome I 60 1.000
737
c LYN004 Lynch Syndrome I 60 1.000
738
P ALP009 Alopecia Areata 60 1.000
739
LGG001 Legg-Calve-Perthes Disease 60 1.000
740
c WLF013 Wolfram Syndrome 1 60 1.000
741
STR039 Sturge-Weber Syndrome 60 1.000
742
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 1.000
743
SQM006 Squamous Cell Carcinoma 60 1.000
744
P ATR010 Atrial Heart Septal Defect 60 1.000
745
P WLF004 Wolfram Syndrome 60 1.000
746
c MSC170 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2 60 1.000
747
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 1.000
748
END081 Endosteal Hyperostosis, Autosomal Dominant 60 1.000
749
DNG002 Dengue Hemorrhagic Fever 60 1.000
750
LBR030 Leber Optic Atrophy 60 1.000
751
c MLT159 Multiple Endocrine Neoplasia, Type Iib 60 1.000
752
RHM001 Rheumatic Fever 60 1.000
753
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 1.000
754
PMS001 Poems Syndrome 60 1.000
755
P SNS001 Sensorineural Hearing Loss 60 1.000
756
VRC005 Varicose Veins 60 1.000
757
CHC001 Chickenpox 60 1.000
758
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 1.000
759
c HYP731 Hyperaldosteronism, Familial, Type I 60 1.000
760
P CTR002 Cataract 60 1.000
761
P PTN014 Patent Ductus Arteriosus 1 60 1.000
762
P USH001 Usher Syndrome 60 1.000
763
P EMR001 Emery-Dreifuss Muscular Dystrophy 60 1.000
764
ORL011 Oral Cancer 60 1.000
765
ING001 Inguinal Hernia 60 1.000
766
INS001 Insulinoma 60 1.000
767
HYD002 Hydronephrosis 60 1.000
768
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 1.000
769
P SHR074 Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly 60 1.000
770
QFV001 Q Fever 60 1.000
771
STF001 Stiff-Person Syndrome 60 1.000
772
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 1.000
773
P OCL002 Oculocutaneous Albinism 60 1.000
774
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 1.000
775
ETN001 Eating Disorder 60 1.000
776
P GLY013 Glycogen Storage Disease 60 1.000
777
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 60 1.000
778
STT001 Status Epilepticus 60 1.000
779
c ACT071 Acute Kidney Failure 60 1.000
780
NRF008 Neurofibromatosis-Noonan Syndrome 60 1.000
781
OCC006 Occipital Horn Syndrome 60 1.000
782
P THL005 Thalassemia 60 1.000
783
P CHR285 Chronic Myelomonocytic Leukemia 60 1.000
784
DRR014 Darier-White Disease 60 1.000
785
VGN017 Vaginal Cancer 60 1.000
786
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.000
787
P HRD011 Hereditary Spherocytosis 60 1.000
788
c OTP006 Otopalatodigital Syndrome, Type I 60 1.000
789
DYS164 Dyskeratosis Congenita, X-Linked 60 1.000
790
FCT002 Factor Xi Deficiency 60 1.000
791
MRT001 Muir-Torre Syndrome 60 1.000
792
NLP001 Nail-Patella Syndrome 60 1.000
793
c HRD002 Hereditary Angioedema 60 1.000
794
P BRN019 Bernard-Soulier Syndrome 60 1.000
795
P OPT006 Optic Nerve Disease 60 1.000
796
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 1.000
797
ANT009 Antithrombin Iii Deficiency 59 1.000
798
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 1.000
799
c ALB021 Albinism, Oculocutaneous, Type Ii 59 1.000
800
SPP011 Suppression of Tumorigenicity 12 59 1.000
801
P RBL001 Rubella 59 1.000
802
P EPS003 Episodic Ataxia 59 1.000
803
P MYC008 Myocarditis 59 1.000
804
P AXN002 Axenfeld-Rieger Syndrome 59 1.000
805
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 59 1.000
806
PBL005 Piebald Trait 59 1.000
807
PRT013 Portal Hypertension 59 1.000
808
CRT002 Cartilage-Hair Hypoplasia 59 1.000
809
P MCR010 Microcephaly 59 1.000
810
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 59 1.000
811
CHL014 Cholera 59 1.000
812
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 59 1.000
813
PRC038 Precocious Puberty, Male-Limited 59 1.000
814
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 1.000
815
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 59 1.000
816
c GLY003 Glycogen Storage Disease Iii 59 1.000
817
P BND020 Bone Disease 59 1.000
818
IDP011 Idiopathic Interstitial Pneumonia 59 1.000
819
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 59 1.000
820
PNM001 Pneumocystosis 59 1.000
821
c HPT016 Hepatitis B 59 1.000
822
P LKD001 Leukodystrophy 59 1.000
823
P BRN022 Bronchiectasis 59 1.000
824
WLF002 Wolf-Hirschhorn Syndrome 59 1.000
825
LGS001 Legius Syndrome 59 1.000
826
c PCH015 Pachyonychia Congenita 1 59 1.000
827
THY029 Thyroid Carcinoma 59 1.000
828
P CMR001 Camurati-Engelmann Disease 59 1.000
829
LKN001 Leukoencephalopathy with Vanishing White Matter 59 1.000
830
IGR001 Ige Responsiveness, Atopic 59 1.000
831
MTC097 Mitochondrial Complex Iv Deficiency 59 1.000
832
c DNG003 Dengue Disease 59 1.000
833
SPN027 Spinal Stenosis 59 1.000
834
P SPN309 Spinocerebellar Ataxia 6 59 1.000
835
UTR024 Uterine Carcinosarcoma 59 1.000
836
MYP136 Myopathy, Centronuclear, X-Linked 59 1.000
837
P SLP005 Sleep Disorder 59 1.000
838
CHL123 Chlamydia 59 1.000
839
P DBT100 Diabetes Mellitus, Permanent Neonatal 1 59 1.000
840
PLM033 Pulmonary Embolism 59 1.000
841
PRT058 Pure Autonomic Failure 59 1.000
842
PRN019 Perinatal Necrotizing Enterocolitis 59 1.000
843
P EPD062 Epidermolysis Bullosa, Junctional, Non-Herlitz Type 59 1.000
844
P PRD006 Prader-Willi Syndrome 59 1.000
845
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 59 1.000
846
P LYM033 Lymphoproliferative Syndrome 59 1.000
847
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 1.000
848
PRG009 Progressive Multifocal Leukoencephalopathy 59 1.000
849
P MLN069 Melanoma, Uveal 59 1.000
850
c LTN004 Late-Onset Retinal Degeneration 59 1.000
851
BLL001 Baller-Gerold Syndrome 59 1.000
852
DCT002 Ductal Carcinoma in Situ 59 1.000
853
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 1.000
854
P WRD001 Waardenburg's Syndrome 59 1.000
855
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 1.000
856
DBN001 Dubin-Johnson Syndrome 59 1.000
857
c MCP045 Mucopolysaccharidosis, Type Iiic 59 1.000
858
P BRS044 Breast Adenocarcinoma 59 1.000
859
P ERY058 Erythrocytosis, Familial, 1 59 1.000
860
GRD007 Grade Iii Astrocytoma 59 1.000
861
P CYS018 Cystitis 59 1.000
862
DNN001 Danon Disease 59 1.000
863
c HYD046 Hydatidiform Mole, Recurrent, 1 59 1.000
864
KLP010 Klippel-Trenaunay-Weber Syndrome 59 1.000
865
AVN001 Avian Influenza 59 1.000
866
ALX003 Alexander Disease 59 1.000
867
GRY002 Gray Platelet Syndrome 59 1.000
868
P HMN036 Hemangiopericytoma, Malignant 59 1.000
869
GNG013 Gingivitis 59 1.000
870
BRN002 Bronchiolitis 59 1.000
871
P CNT004 Centronuclear Myopathy 59 1.000
872
IRN001 Iron Deficiency Anemia 59 1.000
873
P NMN002 Niemann-Pick Disease 59 1.000
874
P GLL022 Guillain-Barre Syndrome 59 1.000
875
P DNG005 Dengue Virus 59 1.000
876
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 59 1.000
877
ADN018 Adenoma 59 1.000
878
CYS010 Cystinosis 59 1.000
879
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 1.000
880
FRB001 Farber Lipogranulomatosis 59 1.000
881
VLV032 Vulva Cancer 59 1.000
882
P NPH005 Nephronophthisis 59 1.000
883
GST045 Gastroenteritis 59 1.000
884
P LDD007 Liddle Syndrome 1 59 1.000
885
c MCP044 Mucopolysaccharidosis, Type Iiib 59 1.000
886
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 1.000
887
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 59 1.000
888
HLC007 Helicobacter Pylori Infection 59 1.000
889
WVR001 Weaver Syndrome 59 1.000
890
P ADM011 Adams-Oliver Syndrome 59 1.000
891
P PLY006 Polydactyly 59 1.000
892
ANR040 Aneurysm 59 1.000
893
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 59 1.000
894
MNK003 Muenke Syndrome 59 1.000
895
c SVR003 Severe Congenital Neutropenia 59 1.000
896
ALP097 Alopecia Universalis Congenita 59 1.000
897
c CLR131 Ciliary Dyskinesia, Primary, 1 59 1.000
898
PPT005 Peptic Ulcer Disease 59 1.000
899
SRC027 Sarcoma, Synovial 58 1.000
900
RNL024 Renal Glucosuria 58 1.000
901
CLS005 Clouston Syndrome 58 1.000
902
INC002 Inclusion Body Myositis 58 1.000
903
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.000
904
DBT087 Diabetes Insipidus, Neurohypophyseal 58 1.000
905
P FML052 Familial Cold Autoinflammatory Syndrome 58 1.000
906
KRT071 Keratosis, Seborrheic 58 1.000
907
PSD012 Pseudoachondroplasia 58 1.000
908
P PLY017 Polyarteritis Nodosa 58 1.000
909
c ACT073 Acute Leukemia 58 1.000
910
P SYP003 Syphilis 58 1.000
911
c GLY007 Glycogen Storage Disease Iv 58 1.000
912
PPL048 Papillorenal Syndrome 58 1.000
913
P ANP001 Anaplastic Large Cell Lymphoma 58 1.000
914
GLB001 Gilbert Syndrome 58 1.000
915
c SPN301 Spinocerebellar Ataxia 2 58 1.000
916
CRY005 Cryptococcosis 58 1.000
917
P TYR004 Tyrosinemia 58 1.000
918
ALK013 Alkaptonuria 58 1.000
919
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 1.000
920
CSY001 C Syndrome 58 1.000
921
c LNG047 Long Qt Syndrome 2 58 1.000
922
ANT024 Anthrax Disease 58 1.000
923
P INT070 Intestinal Obstruction 58 1.000
924
P HYP726 Hypercalcemia, Infantile, 1 58 1.000
925
c NMN016 Niemann-Pick Disease, Type B 58 1.000
926
PRX015 Paroxysmal Extreme Pain Disorder 58 1.000
927
RBS001 Rabies 58 1.000
928
ERY029 Erythermalgia, Primary 58 1.000
929
P PGT001 Paget's Disease of Bone 58 1.000
930
PRM057 Paramyotonia Congenita of Von Eulenburg 58 1.000
931
c LYS021 Loeys-Dietz Syndrome 3 58 1.000
932
P BCL017 B-Cell Lymphoma 58 1.000
933
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 1.000
934
SPR004 Supravalvular Aortic Stenosis 58 1.000
935
c XRD022 Xeroderma Pigmentosum, Complementation Group D 58 1.000
936
FBR047 Fibromyalgia 58 1.000
937
CMP010 Complex Regional Pain Syndrome 58 1.000
938
c SHR072 Short-Rib Thoracic Dysplasia 3 with or Without Polydactyly 58 1.000
939
TTZ003 Tietz Albinism-Deafness Syndrome 58 1.000
940
c CHL140 Chilblain Lupus 1 58 1.000
941
FCL081 Focal Cortical Dysplasia, Type Ii 58 1.000
942
P MLT007 Multiple Epiphyseal Dysplasia 58 1.000
943
CRD132 Cardiac Conduction Defect 58 1.000
944
CHR072 Chordoma 58 1.000
945
MCS006 Macs Syndrome 58 1.000
946
SCR008 Scrub Typhus 58 1.000
947
THY025 Thymus Cancer 58 1.000
948
c BNG091 Benign Chronic Pemphigus 58 1.000
949
FML063 Familial Glucocorticoid Deficiency 58 1.000
950
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 1.000
951
DST005 Diastrophic Dysplasia 58 1.000
952
P STR022 Stargardt Disease 58 1.000
953
c PRG018 Paragangliomas 1 58 1.000
954
c PTT056 Pituitary Adenoma 1, Multiple Types 58 1.000
955
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 1.000
956
SPT004 Septic Arthritis 58 1.000
957
P ALC033 Alcohol Use Disorder 58 1.000
958
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 58 1.000
959
c PRM005 Primary Hyperparathyroidism 58 1.000
960
CCC001 Coccidioidomycosis 58 1.000
961
P EPD083 Epidermodysplasia Verruciformis 1 58 1.000
962
HYP458 Hyper Ige Syndrome 58 1.000
963
RSP019 Respiratory Distress Syndrome in Premature Infants 58 1.000
964
CNT047 Contact Dermatitis 58 1.000
965
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.000
966
PLM026 Pilomatrixoma 58 1.000
967
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 1.000
968
BRS051 Breast Disease 58 1.000
969
ADR005 Adrenal Carcinoma 58 1.000
970
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 58 1.000
971
ERY003 Erythema Multiforme 58 1.000
972
P URT039 Urticaria 58 1.000
973
P MTR012 Mitral Valve Disease 58 1.000
974
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.000
975
ADL030 Adult-Onset Still's Disease 58 1.000
976
P EHL001 Ehlers-Danlos Syndrome 58 1.000
977
NWB001 Newborn Respiratory Distress Syndrome 58 1.000
978
EYD002 Eye Disease 58 1.000
979
DSS008 Disease of Mental Health 58 1.000
980
P MMP001 Mumps 58 1.000
981
CRV038 Cervical Squamous Cell Carcinoma 58 1.000
982
c GLC097 Glaucoma 3, Primary Congenital, a 58 1.000
983
MNT002 Mental Depression 58 1.000
984
P PTY003 Pityriasis Rubra Pilaris 58 1.000
985
CHL028 Childhood Type Dermatomyositis 58 1.000
986
P BNC003 Bone Cancer 58 1.000
987
CNS004 Constipation 58 1.000
988
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 58 1.000
989
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 1.000
990
c DWL002 Dowling-Degos Disease 1 58 1.000
991
APP015 Apparent Mineralocorticoid Excess 58 1.000
992
P EPD003 Epidermolysis Bullosa Simplex 58 1.000
993
LYM027 Lymphopenia 58 1.000
994
P CND004 Candidiasis 58 1.000
995
BRG013 Buerger Disease 58 1.000
996
EXT034 Extrinsic Allergic Alveolitis 58 1.000
997
P PRP019 Peripheral Nervous System Disease 58 1.000
998
MRS002 Marshall Syndrome 58 1.000
999
LNG108 Langerhans Cell Histiocytosis 58 1.000
1000
MXD005 Mixed Connective Tissue Disease 58 1.000
1001
P VND007 Van Der Woude Syndrome 1 58 1.000
1002
c THY102 Thyroid Cancer, Nonmedullary, 2 58 1.000
1003
c MCP004 Mucopolysaccharidosis Iv 57 1.000
1004
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 1.000
1005
CHR081 Choroideremia 57 1.000
1006
P GLL018 Gallbladder Cancer 57 1.000
1007
P FNC044 Fanconi Anemia, Complementation Group C 57 1.000
1008
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 57 1.000
1009
P INF032 Infertility 57 1.000
1010
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 1.000
1011
P UVT001 Uveitis 57 1.000
1012
PMP006 Pemphigus Vulgaris, Familial 57 1.000
1013
P GLL020 Gallbladder Disease 57 1.000
1014
P ESP035 Esophagitis, Eosinophilic, 1 57 1.000
1015
GYR004 Gyrate Atrophy of Choroid and Retina 57 1.000
1016
APL002 Aplasia of Lacrimal and Salivary Glands 57 1.000
1017
DNY001 Denys-Drash Syndrome 57 1.000
1018
P GLM007 Glomerulonephritis 57 1.000
1019
GLS018 Glass Syndrome 57 1.000
1020
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 1.000
1021
P OPT009 Optic Neuritis 57 1.000
1022
TTL012 Total Anomalous Pulmonary Venous Return 1 57 1.000
1023
P PLV020 Pelvic Organ Prolapse 57 1.000
1024
CST005 Castleman Disease 57 1.000
1025
c CHR417 Chronic Graft Versus Host Disease 57 1.000
1026
BLM002 Bulimia Nervosa 57 1.000
1027
MCR013 Microphthalmia 57 1.000
1028
c CHL119 Cholangitis, Primary Sclerosing 57 1.000
1029
GRN051 Granulomatous Disease, Chronic, X-Linked 57 1.000
1030
CHL067 Cholecystitis 57 1.000
1031
P ZLL001 Zellweger Syndrome 57 1.000
1032
IRN002 Iron Metabolism Disease 57 1.000
1033
c ANM036 Anemia, Sideroblastic, 1 57 1.000
1034
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 57 1.000
1035
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 57 1.000
1036
BRN056 Bronchopulmonary Dysplasia 57 1.000
1037
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 1.000
1038
MNR012 Meniere Disease 57 1.000
1039
c LYS019 Loeys-Dietz Syndrome 1 57 1.000
1040
c VSC019 Vesicoureteral Reflux 1 57 1.000
1041
P MYM013 Moyamoya Disease 1 57 1.000
1042
PLM070 Pulmonic Stenosis 57 1.000
1043
P PLY041 Polymyositis 57 1.000
1044
CHR003 Cherubism 57 1.000
1045
P EXN002 Exanthem 57 1.000
1046
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 1.000
1047
CHK001 Chikungunya 57 1.000
1048
P RHN004 Rhinitis 57 1.000
1049
P SLV026 Salivary Gland Carcinoma 57 1.000
1050
ARG007 Argininemia 57 1.000