Search results for Inositol

720 hits were found for Inositol

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 65 0.388
2
P PLY011 Polycystic Ovary Syndrome 56 0.378
3
P NRB001 Neuroblastoma 72 0.257
4
P BPL003 Bipolar Disorder 56 0.251
5
c MJR024 Major Affective Disorder 9 41 0.251
6
c MJR022 Major Affective Disorder 8 38 0.251
7
GST033 Gestational Diabetes 61 0.204
8
c PLY105 Polycystic Ovary Syndrome 1 38 0.183
9
HYP043 Hyperandrogenism 48 0.174
10
ANV001 Anovulation 47 0.172
11
CHL014 Cholera 59 0.170
12
HYP060 Hyperinsulinism 54 0.166
13
P INF032 Infertility 57 0.158
14
P GLM045 Glioma 63 0.154
15
NRL016 Neural Tube Defects 82 0.152
16
GLL048 Glial Tumor 45 0.152
17
HYP066 Hyperglycemia 61 0.146
18
DPR016 Depression 63 0.136
19
DBT010 Diabetic Neuropathy 54 0.136
20
P AST007 Astrocytoma 51 0.136
21
P CLR023 Colorectal Cancer 99 0.132
22
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.129
23
c EXD008 Exudative Vitreoretinopathy 1 71 0.129
24
OBS002 Obsessive-Compulsive Disorder 68 0.127
25
FTT001 Fatty Liver Disease 61 0.127
26
P ALZ034 Alzheimer Disease 88 0.124
27
MNT002 Mental Depression 58 0.124
28
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.124
29
DWN001 Down Syndrome 70 0.122
30
BRN056 Bronchopulmonary Dysplasia 57 0.119
31
c KNN009 Kenny-Caffey Syndrome, Type 1 34 0.119
32
P DBT009 Diabetes Mellitus 64 0.116
33
GLC003 Glucose Intolerance 54 0.116
34
P PNC025 Panic Disorder 53 0.116
35
c PRC016 Pre-Eclampsia 63 0.113
36
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.113
37
P HYP086 Hypothyroidism 69 0.108
38
VSL002 Visual Epilepsy 59 0.104
39
P NRP001 Neuropathy 56 0.104
40
P SZR006 Seizure Disorder 56 0.104
41
P MJR007 Major Affective Disorder 1 43 0.104
42
P HNT016 Huntington Disease 72 0.101
43
OST159 Osteogenic Sarcoma 66 0.101
44
HYP056 Hypoglycemia 66 0.101
45
INS001 Insulinoma 60 0.101
46
P PHC003 Pheochromocytoma 71 0.098
47
P CTR002 Cataract 60 0.098
48
c MCR113 Microvascular Complications of Diabetes 3 52 0.098
49
c MCR120 Microvascular Complications of Diabetes 7 47 0.098
50
ADR040 Adrenal Gland Pheochromocytoma 46 0.098
51
c MCR130 Microvascular Complications of Diabetes 6 41 0.098
52
c MCR133 Microvascular Complications of Diabetes 4 41 0.098
53
PPL052 Papillomatosis, Confluent and Reticulated 33 0.098
54
INS024 Insulin-Like Growth Factor I 79 0.095
55
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.095
56
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.095
57
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.095
58
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.095
59
c NRF023 Neurofibromatosis, Type Ii 80 0.091
60
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.091
61
P SCH015 Schizophrenia 74 0.091
62
c RHB024 Rhabdomyosarcoma 2 67 0.091
63
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.091
64
MDD011 Mood Disorder 62 0.091
65
ERY051 Erythroleukemia, Familial 56 0.091
66
WHP001 Whipple Disease 49 0.091
67
CHR178 Chromosomal Triplication 35 0.091
68
P PRS040 Prostate Cancer 97 0.088
69
GLB015 Glioblastoma Multiforme 75 0.088
70
P KDN018 Kidney Disease 72 0.088
71
OVR029 Ovarian Hyperstimulation Syndrome 64 0.088
72
P MLN007 Male Infertility 55 0.088
73
HLX001 Helix Syndrome 47 0.088
74
P BRS047 Breast Cancer 97 0.084
75
BNR002 Bone Resorption Disease 48 0.084
76
P MJR001 Major Depressive Disorder 68 0.080
77
P MLG056 Malignant Hyperthermia 67 0.080
78
AMN001 Amenorrhea 54 0.080
79
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.080
80
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.080
81
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.080
82
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.080
83
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.080
84
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.080
85
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.080
86
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.080
87
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.080
88
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.080
89
CHL079 Children's Interstitial Lung Disease 26 0.080
90
P LNG032 Lung Cancer 98 0.076
91
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.076
92
CHG001 Chagas Disease 66 0.076
93
LPD008 Lipid Metabolism Disorder 62 0.076
94
SQM006 Squamous Cell Carcinoma 60 0.076
95
ADN018 Adenoma 59 0.076
96
CYT002 Cytokine Deficiency 42 0.076
97
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.076
98
P OVR042 Ovarian Cancer 88 0.072
99
ANX010 Anxiety 73 0.072
100
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.072
101
P GLC113 Galactosemia I 64 0.072
102
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.072
103
P VSC007 Vascular Disease 63 0.072
104
LVR012 Liver Cirrhosis 62 0.072
105
NTR005 Nutritional Deficiency Disease 62 0.072
106
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.072
107
P BCL017 B-Cell Lymphoma 58 0.072
108
HYP266 Hypoxia 57 0.072
109
P MYP006 Myopia 55 0.072
110
P STR020 Strabismus 55 0.072
111
P OVR049 Ovarian Disease 52 0.072
112
AMB002 Amblyopia 49 0.072
113
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.072
114
MCH006 Mechanical Strabismus 42 0.072
115
SPP007 Suppression Amblyopia 39 0.072
116
c MJR008 Major Affective Disorder 2 35 0.072
117
c MJR023 Major Affective Disorder 7 33 0.072
118
c MJR003 Major Affective Disorder 6 33 0.072
119
c MJR006 Major Affective Disorder 5 33 0.072
120
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.072
121
c MJR004 Major Affective Disorder 4 28 0.072
122
PRX085 Preaxial Hallucal Polydactyly 28 0.072
123
P TRN020 Turner Syndrome 67 0.067
124
TTN003 Tetanus 65 0.067
125
CHL068 Cholestasis 61 0.067
126
P ENC018 Encephalopathy 61 0.067
127
HPT019 Hepatic Encephalopathy 60 0.067
128
PRN019 Perinatal Necrotizing Enterocolitis 59 0.067
129
P ALP008 Alopecia 54 0.067
130
P THY032 Thyroiditis 52 0.067
131
ENT011 Enterocolitis 51 0.067
132
HPT004 Hepatic Coma 45 0.067
133
PTT037 Pituitary Tumors 44 0.067
134
FNG004 Fungal Meningitis 44 0.067
135
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.067
136
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.067
137
HRW001 Hair Whorl 36 0.067
138
P HPT023 Hepatocellular Carcinoma 100 0.062
139
c LKM061 Leukemia, Acute Myeloid 84 0.062
140
P PNC035 Pancreatic Cancer 84 0.062
141
CYS001 Cystic Fibrosis 81 0.062
142
P BLD134 Bladder Cancer 79 0.062
143
P RSP003 Respiratory Failure 74 0.062
144
c HYP836 Hypercholesterolemia, Familial, 1 73 0.062
145
P ATS364 Autism 70 0.062
146
P LVR013 Liver Disease 68 0.062
147
P MSC005 Muscular Dystrophy 66 0.062
148
P SKN015 Skin Carcinoma 66 0.062
149
P AGM001 Agammaglobulinemia 65 0.062
150
P PRD008 Periodontitis 64 0.062
151
P PLY014 Polycystic Kidney Disease 62 0.062
152
HSH003 Hashimoto Thyroiditis 62 0.062
153
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.062
154
NPH009 Nephrolithiasis 55 0.062
155
END040 Endogenous Depression 55 0.062
156
SLP001 Sleeping Sickness 54 0.062
157
LNG031 Lung Benign Neoplasm 51 0.062
158
HMG002 Hemoglobinuria 50 0.062
159
47X002 47,xyy 49 0.062
160
c SPR086 Spermatogenic Failure 3 44 0.062
161
48X005 48,xyyy 39 0.062
162
OLG022 Oligoasthenoteratozoospermia 36 0.062
163
c HYP595 Hypertension, Essential 84 0.057
164
P ATX030 Ataxia-Telangiectasia 82 0.057
165
IMM167 Immune Deficiency Disease 78 0.057
166
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.057
167
SVR004 Severe Combined Immunodeficiency 73 0.057
168
ULC004 Ulcerative Colitis 73 0.057
169
P RTN024 Retinoblastoma 73 0.057
170
MSC157 Muscular Dystrophy, Duchenne Type 72 0.057
171
P JBR020 Joubert Syndrome 1 72 0.057
172
P MLN008 Melanoma 69 0.057
173
c SML038 Small Cell Cancer of the Lung 65 0.057
174
P ADN016 Adenocarcinoma 64 0.057
175
HYP020 Hyperprolactinemia 64 0.057
176
CLT003 Colitis 62 0.057
177
P PSR002 Psoriasis 62 0.057
178
INT002 Intermittent Claudication 61 0.057
179
c ACT027 Acute Pancreatitis 60 0.057
180
LNG099 Lung Disease 60 0.057
181
P ALP009 Alopecia Areata 60 0.057
182
STT001 Status Epilepticus 60 0.057
183
ISC004 Ischemia 58 0.057
184
P PRP019 Peripheral Nervous System Disease 58 0.057
185
P FBR017 Fibrosarcoma 56 0.057
186
ANN002 Anencephaly 56 0.057
187
P ART021 Arteriosclerosis 54 0.057
188
c PRD040 Periodontitis, Chronic 53 0.057
189
c FML008 Familial Retinoblastoma 53 0.057
190
PST011 Pustulosis of Palm and Sole 52 0.057
191
TLN003 Telangiectasis 52 0.057
192
TRC010 Trichotillomania 51 0.057
193
CLC006 Calcinosis 48 0.057
194
P OCY003 Oocyte Maturation Defect 1 45 0.057
195
CLP005 Ciliopathy 43 0.057
196
ORL015 Oral Squamous Cell Carcinoma 43 0.057
197
c SPN290 Spinocerebellar Ataxia 15 40 0.057
198
c CHL142 Cholestasis, Intrahepatic, of Pregnancy 3 38 0.057
199
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.051
200
P LKM071 Leukemia, Chronic Lymphocytic 79 0.051
201
END057 Endometrial Cancer 74 0.051
202
AGM019 Agammaglobulinemia, X-Linked 71 0.051
203
c CHR684 Chronic Kidney Disease 70 0.051
204
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.051
205
PSY004 Psychotic Disorder 67 0.051
206
ATH013 Atherosclerosis Susceptibility 65 0.051
207
c DBT099 Diabetes Mellitus, Type I 65 0.051
208
CLN015 Colon Adenocarcinoma 65 0.051
209
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.051
210
LSH001 Leishmaniasis 63 0.051
211
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.051
212
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.051
213
P CRD246 Cardiovascular System Disease 57 0.051
214
c ACT134 Acute Liver Failure 56 0.051
215
BCT022 Bacterial Infectious Disease 56 0.051
216
BRN004 Brain Edema 56 0.051
217
P PLY019 Polyneuropathy 56 0.051
218
P LTR001 Lateral Sclerosis 54 0.051
219
P TRM003 Tremor 54 0.051
220
NNL006 Non-Alcoholic Steatohepatitis 54 0.051
221
P ECL001 Eclampsia 50 0.051
222
HPT014 Hepatorenal Syndrome 50 0.051
223
PLC008 Placenta Disease 50 0.051
224
MNN009 Meningoencephalitis 49 0.051
225
BRN071 Brain Injury 49 0.051
226
c BPL002 Bipolar I Disorder 49 0.051
227
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.051
228
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.051
229
c PCH010 Pachyonychia Congenita 3 44 0.051
230
FTL021 Fetal Macrosomia 42 0.051
231
P KLZ004 Kala-Azar 1 41 0.051
232
ALL014 Allergic Encephalomyelitis 38 0.051
233
OPS002 Opsismodysplasia 37 0.051
234
TTH004 Tethered Spinal Cord Syndrome 35 0.051
235
CND006 Candida Glabrata 32 0.051
236
CNN003 Conn's Syndrome 79 0.044
237
GST019 Gastrointestinal Stromal Tumor 78 0.044
238
P LNG064 Lung Cancer Susceptibility 3 78 0.044
239
P APL001 Aplastic Anemia 74 0.044
240
CRH001 Crohn's Disease 74 0.044
241
P NJM001 Nijmegen Breakage Syndrome 74 0.044
242
P LYM118 Lymphoma 68 0.044
243
CHL065 Cholangiocarcinoma 68 0.044
244
P LKM002 Leukemia 68 0.044
245
c INF071 Inflammatory Bowel Disease 1 67 0.044
246
c ATS007 Autism Spectrum Disorder 67 0.044
247
ALC007 Alcohol Dependence 66 0.044
248
P MCR115 Microvascular Complications of Diabetes 5 66 0.044
249
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.044
250
SRC014 Sarcoma 65 0.044
251
P MCH002 Machado-Joseph Disease 62 0.044
252
c BRN108 Branchiootic Syndrome 1 62 0.044
253
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.044
254
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.044
255
P MYL006 Myeloid Leukemia 60 0.044
256
P NPH012 Nephrotic Syndrome 60 0.044
257
DPH001 Diphtheria 60 0.044
258
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.044
259
ETN001 Eating Disorder 60 0.044
260
PNM001 Pneumocystosis 59 0.044
261
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.044
262
GNG013 Gingivitis 59 0.044
263
P PLY006 Polydactyly 59 0.044
264
BRS051 Breast Disease 58 0.044
265
NWB001 Newborn Respiratory Distress Syndrome 58 0.044
266
DSS008 Disease of Mental Health 58 0.044
267
P CND004 Candidiasis 58 0.044
268
P GLM007 Glomerulonephritis 57 0.044
269
IRN002 Iron Metabolism Disease 57 0.044
270
P PRV006 Pervasive Developmental Disorder 57 0.044
271
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.044
272
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.044
273
P DRR001 Diarrhea 55 0.044
274
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.044
275
P GRV001 Graves' Disease 55 0.044
276
P HYP076 Hyperthyroidism 55 0.044
277
CRH005 Crohn's Colitis 53 0.044
278
SPN035 Spindle Cell Sarcoma 53 0.044
279
c PSR017 Psoriasis 2 53 0.044
280
P RTN018 Retinal Disease 53 0.044
281
c PSR023 Psoriasis 1 52 0.044
282
P OLV001 Olivopontocerebellar Atrophy 51 0.044
284
OCL069 Ocular Motor Apraxia 51 0.044
285
INT079 Intrahepatic Cholangiocarcinoma 51 0.044
286
P OVR082 Overgrowth Syndrome 50 0.044
287
STM007 Stomatitis 50 0.044
288
P SCK005 Sickle Cell Disease 50 0.044
289
LRN003 Learning Disability 49 0.044
290
ATS010 Autosomal Recessive Disease 48 0.044
291
c PSR032 Psoriasis 11 47 0.044
292
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.044
293
RYN005 Raynaud Phenomenon 47 0.044
294
GLC022 Glucose/galactose Malabsorption 45 0.044
295
IMP006 Impulse Control Disorder 45 0.044
296
AGR002 Agoraphobia 45 0.044
297
P SBR004 Seborrheic Dermatitis 45 0.044
298
c PSR028 Psoriasis 7 42 0.044
299
c PSR018 Psoriasis 13 41 0.044
300
HYP344 Hyperthyroidism, Familial Gestational 39 0.044
301
DBT007 Diabetic Cataract 38 0.044
302
c LKM005 Leukemia, T-Cell, Chronic 34 0.044
303
P GST053 Gastric Cancer 83 0.036
304
MLR004 Malaria 81 0.036
305
P GLM040 Glioma Susceptibility 1 81 0.036
306
P HRT032 Heart Disease 75 0.036
307
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.036
308
BRN028 Brain Cancer 74 0.036
309
P OST002 Osteoporosis 74 0.036
310
P CNR004 Cone-Rod Dystrophy 2 73 0.036
311
P MLT020 Multiple Sclerosis 72 0.036
312
HMN044 Human Immunodeficiency Virus Type 1 71 0.036
313
PRP027 Peripheral Vascular Disease 71 0.036
314
P MYC007 Myocardial Infarction 70 0.036
315
P MYP004 Myopathy 70 0.036
316
P LKM062 Leukemia, Acute Lymphoblastic 69 0.036
317
P MYC084 Mycobacterium Tuberculosis 1 68 0.036
318
SKN019 Skin Melanoma 68 0.036
319
RCK004 Rickets 68 0.036
320
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.036
321
P OLG002 Oligodendroglioma 67 0.036
322
BRK010 Burkitt Lymphoma 67 0.036
323
CRB039 Cerebrovascular Disease 67 0.036
324
P PLM037 Pulmonary Hypertension 67 0.036
325
c MGR028 Migraine with or Without Aura 1 67 0.036
326
ANG054 Angina Pectoris 66 0.036
327
P ATR011 Atrial Fibrillation 66 0.036
328
LNG039 Lung Squamous Cell Carcinoma 66 0.036
329
P PLM036 Pulmonary Fibrosis 65 0.036
330
IRR002 Irritable Bowel Syndrome 65 0.036
331
KWS002 Kawasaki Disease 65 0.036
332
P THY023 Thymoma 65 0.036
333
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.036
334
P RHB003 Rhabdomyosarcoma 63 0.036
335
P HML002 Hemolytic Anemia 63 0.036
336
CNT061 Conotruncal Heart Malformations 63 0.036
337
c SVR001 Severe Acute Respiratory Syndrome 62 0.036
338
P HYP750 Hypertriglyceridemia, Familial 62 0.036
339
P DNT020 Dent Disease 1 62 0.036
340
BLL006 Bullous Pemphigoid 62 0.036
341
TXC005 Toxic Shock Syndrome 62 0.036
342
MSL001 Measles 62 0.036
343
P INT143 Interstitial Cystitis 61 0.036
344
c PNS012 Paine Syndrome 61 0.036
345
c SCL052 Scleroderma, Familial Progressive 61 0.036
346
P ENC004 Encephalitis 61 0.036
347
ORL011 Oral Cancer 60 0.036
348
c ACT071 Acute Kidney Failure 60 0.036
349
PRT013 Portal Hypertension 59 0.036
350
P LYM033 Lymphoproliferative Syndrome 59 0.036
351
c LTN004 Late-Onset Retinal Degeneration 59 0.036
352
P CYS018 Cystitis 59 0.036
353
P NPH005 Nephronophthisis 59 0.036
354
GST045 Gastroenteritis 59 0.036
355
CRY005 Cryptococcosis 58 0.036
356
P URT039 Urticaria 58 0.036
357
MCR013 Microphthalmia 57 0.036
358
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.036
359
P FCL005 Focal Segmental Glomerulosclerosis 57 0.036
360
ALL006 Allergic Asthma 56 0.036
361
SCH003 Schizophreniform Disorder 56 0.036
362
HYP005 Hypokalemia 55 0.036
363
FND002 Fundus Dystrophy 55 0.036
364
P SLM003 Salmonellosis 55 0.036
365
P PMP001 Pemphigus 54 0.036
366
AMN003 Amnestic Disorder 54 0.036
367
P INF037 Inflammatory Bowel Disease 54 0.036
368
PLM010 Pulmonary Edema 54 0.036
369
PRS045 Prostatic Hypertrophy 53 0.036
370
P FBR031 Febrile Seizures 53 0.036
371
P ACT008 Actinic Keratosis 53 0.036
372
NRT001 Neurotic Disorder 53 0.036
373
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.036
374
DMY004 Demyelinating Disease 52 0.036
375
GLM004 Gliomatosis Cerebri 52 0.036
376
THY030 Thyroid Gland Disease 52 0.036
377
P MSC003 Muscular Atrophy 52 0.036
378
c THY107 Thymoma, Familial 52 0.036
379
LGN006 Legionnaire Disease 52 0.036
380
c INH030 Inherited Retinal Disorder 51 0.036
381
PRS021 Prostatic Adenoma 51 0.036
382
KRT009 Keratosis 51 0.036
383
CLR109 Colorectal Adenocarcinoma 51 0.036
384
TRM010 Traumatic Brain Injury 51 0.036
385
HYP081 Hypolipoproteinemia 51 0.036
386
P TMP001 Temporal Lobe Epilepsy 50 0.036
387
TRY001 Trypanosomiasis 50 0.036
388
VRC001 Varicocele 49 0.036
389
CRY014 Cryptococcal Meningitis 48 0.036
390
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.036
391
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.036
392
PLY012 Polyhydramnios 46 0.036
393
OLG001 Oligospermia 45 0.036
394
TRT001 Teratocarcinoma 45 0.036
395
CRB004 Cerebral Artery Occlusion 45 0.036
396
CVD001 Covid-19 44 0.036
397
c SPN101 Spinocerebellar Ataxia 29 42 0.036
398
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.036
399
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.036
400
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.036
401
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 41 0.036
402
ANX004 Anoxia 40 0.036
403
AML001 Amelanotic Melanoma 39 0.036
404
LWG005 Low-Grade Astrocytoma 38 0.036
405
PRM329 Premature Aging 35 0.036
406
NRX001 Neuroaxonal Dystrophy 35 0.036
407
PRN007 Perinephritis 33 0.036
408
EXN003 Exencephaly 31 0.036
409
PLY150 Polykaryocytosis Inducer 31 0.036
410
ARG004 Argyria 27 0.036
411
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.036
412
ESP021 Esophageal Cancer 90 0.025
413
MYL069 Myeloma, Multiple 85 0.025
414
STR067 Stroke, Ischemic 81 0.025
415
c DLT002 Dilated Cardiomyopathy 79 0.025
416
P RTN008 Retinitis Pigmentosa 79 0.025
417
P PRK057 Parkinson Disease, Late-Onset 78 0.025
418
CRV035 Cervical Cancer 76 0.025
419
c ATR087 Atrial Standstill 1 75 0.025
420
c ART115 Aortic Valve Disease 1 75 0.025
421
SCK003 Sickle Cell Anemia 74 0.025
422
c MNN043 Meningioma, Familial 74 0.025
423
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.025
424
c THR092 Thrombophilia Due to Thrombin Defect 73 0.025
425
P FML018 Familial Mediterranean Fever 73 0.025
426
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.025
427
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.025
428
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.025
429
P LFR001 Li-Fraumeni Syndrome 72 0.025
430
P GRF003 Graft-Versus-Host Disease 72 0.025
431
ACR007 Acromegaly 71 0.025
432
DFC004 Deficiency Anemia 70 0.025
433
GST040 Gastric Adenocarcinoma 70 0.025
434
P TTR001 Tetralogy of Fallot 70 0.025
435
CRT072 Creutzfeldt-Jakob Disease 70 0.025
436
CNG034 Congestive Heart Failure 69 0.025
437
P SLP006 Sleep Apnea 69 0.025
438
P LPR021 Leprosy 3 69 0.025
439
ART016 Aortic Aneurysm 69 0.025
440
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.025
441
P SYS005 Systemic Scleroderma 68 0.025
442
CMM004 Common Variable Immunodeficiency 68 0.025
443
c BSL007 Basal Cell Carcinoma 68 0.025
444
CNN005 Connective Tissue Disease 68 0.025
445
PNC129 Pancreatic Adenocarcinoma 68 0.025
446
P CRD119 Cardiac Arrest 67 0.025
447
P CRB048 Cerebral Cavernous Malformations 67 0.025
448
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.025
449
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.025
450
P CLC063 Celiac Disease 1 66 0.025
451
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.025
452
P DMN002 Dementia 66 0.025
453
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.025
454
P NSP012 Nasopharyngeal Carcinoma 66 0.025
455
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.025
456
c HRD010 Hereditary Spastic Paraplegia 66 0.025
457
P HYD006 Hydrocephalus 66 0.025
458
P MNN013 Meningitis 66 0.025
459
P DRM053 Dermatitis, Atopic 66 0.025
460
MYL031 Myeloproliferative Neoplasm 66 0.025
461
KHL003 Kohlschutter-Tonz Syndrome 65 0.025
462
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.025
463
c ART101 Aortic Valve Disease 2 65 0.025
464
P CHR071 Charcot-Marie-Tooth Disease 65 0.025
465
PRT036 Peritonitis 64 0.025
466
P HRM001 Hermansky-Pudlak Syndrome 64 0.025
467
CLF027 Cleft Palate, Isolated 64 0.025
468
GT001 Gout 64 0.025
469
CLR108 Colorectal Adenoma 64 0.025
470
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.025
471
PLM031 Poliomyelitis 64 0.025
472
OST017 Osteomyelitis 64 0.025
473
P NTR004 Neutropenia 63 0.025
474
PLG002 Plague 63 0.025
475
P CRN300 Coronary Heart Disease 1 63 0.025
476
P MVM001 Movement Disease 63 0.025
477
P LMY004 Leiomyosarcoma 63 0.025
478
P END044 Endometriosis 63 0.025
479
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.025
480
LPP008 Lipoprotein Quantitative Trait Locus 62 0.025
481
P VSC011 Vasculitis 62 0.025
482
c ANM038 Anemia, Autoimmune Hemolytic 62 0.025
483
ATM095 Autoimmune Disease 62 0.025
484
ALL026 Allergic Hypersensitivity Disease 62 0.025
485
MNN042 Meningioma, Radiation-Induced 62 0.025
486
P KLL001 Kallmann Syndrome 61 0.025
487
NRM001 Neuromyelitis Optica 61 0.025
488
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.025
489
DRM006 Dermatitis 61 0.025
490
ALC006 Alcoholic Hepatitis 61 0.025
491
CHR066 Chronic Fatigue Syndrome 61 0.025
492
P ACH003 Achromatopsia 61 0.025
493
P PNC044 Pancreatitis 61 0.025
494
SPN186 Spinal Cord Injury 60 0.025
495
ACQ007 Acquired Immunodeficiency Syndrome 60 0.025
496
P SNS001 Sensorineural Hearing Loss 60 0.025
497
P THL005 Thalassemia 60 0.025
498
P CHR285 Chronic Myelomonocytic Leukemia 60 0.025
499
P BRN019 Bernard-Soulier Syndrome 60 0.025
500
P MYC008 Myocarditis 59 0.025
501
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.025
502
P BND020 Bone Disease 59 0.025
503
P LKD001 Leukodystrophy 59 0.025
504
P BRN022 Bronchiectasis 59 0.025
505
THY029 Thyroid Carcinoma 59 0.025
506
CHL123 Chlamydia 59 0.025
507
P BRS044 Breast Adenocarcinoma 59 0.025
508
GRD007 Grade Iii Astrocytoma 59 0.025
509
BRN002 Bronchiolitis 59 0.025
510
P CNT004 Centronuclear Myopathy 59 0.025
511
P GLL022 Guillain-Barre Syndrome 59 0.025
512
ANR040 Aneurysm 59 0.025
513
INC002 Inclusion Body Myositis 58 0.025
514
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.025
515
c ACT073 Acute Leukemia 58 0.025
516
P ANP001 Anaplastic Large Cell Lymphoma 58 0.025
517
c SPN301 Spinocerebellar Ataxia 2 58 0.025
518
PST028 Post-Traumatic Stress Disorder 58 0.025
519
FBR047 Fibromyalgia 58 0.025
520
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.025
521
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.025
522
ADR005 Adrenal Carcinoma 58 0.025
523
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.025
524
CNS004 Constipation 58 0.025
525
PMP006 Pemphigus Vulgaris, Familial 57 0.025
526
c CHR417 Chronic Graft Versus Host Disease 57 0.025
527
BLM002 Bulimia Nervosa 57 0.025
528
P PRN023 Prion Disease 57 0.025
529
THR024 Thrombosis 57 0.025
530
CHR177 Chromophobe Renal Cell Carcinoma 57 0.025
531
VSC002 Vascular Dementia 57 0.025
532
CYT008 Cytomegalovirus Infection 57 0.025
533
JPN002 Japanese Encephalitis 57 0.025
534
SCH014 Schistosomiasis 57 0.025
535
P MYS005 Myositis 56 0.025
536
P ADL017 Adult T-Cell Leukemia 56 0.025
537
P CHN012 Chondrosarcoma 56 0.025
538
TCK001 Tick-Borne Encephalitis 56 0.025
539
SFT003 Soft Tissue Sarcoma 56 0.025
540
CYS008 Cystic Echinococcosis 56 0.025
541
EMB004 Embryonal Carcinoma 56 0.025
542
c GRV008 Graves Disease 1 56 0.025
543
P GST044 Gastritis 56 0.025
544
HPT022 Hepatoblastoma 56 0.025
545
BRN012 Bronchiolitis Obliterans 55 0.025
546
P ANT006 Antiphospholipid Syndrome 55 0.025
547
P PTT006 Pituitary Adenoma 55 0.025
548
CHR100 Chronic Ulcer of Skin 55 0.025
549
HDR002 Hidradenitis Suppurativa 55 0.025
550
CRC006 Carcinoid Syndrome 55 0.025
551
P DBT005 Diabetes Insipidus 55 0.025
552
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.025
553
FLT006 Floating-Harbor Syndrome 55 0.025
554
SYN007 Synovitis 54 0.025
555
VGN023 Vaginitis 54 0.025
556
P RST001 Restless Legs Syndrome 54 0.025
557
BRN014 Bronchopneumonia 54 0.025
558
HMS001 Hemosiderosis 54 0.025
559
c SPN294 Spinocerebellar Ataxia 1 53 0.025
560
CLR030 Clear Cell Renal Cell Carcinoma 53 0.025
561
HRT012 Heart Valve Disease 53 0.025
562
IMM102 Immunodeficiency 14 53 0.025
563
P MNC007 Monocytic Leukemia 53 0.025
564
P RNL017 Renal Oncocytoma 53 0.025
565
ECH003 Echinococcosis 53 0.025
566
ACR014 Acral Lentiginous Melanoma 53 0.025
567
P CNT005 Central Nervous System Lymphoma 53 0.025
568
P HMR003 Hemorrhagic Disease 53 0.025
569
CLF001 Cleft Lip 53 0.025
570
GTR002 Goiter 53 0.025
571
HMC014 Homocysteinemia 53 0.025
572
GSG001 Gas Gangrene 53 0.025
573
c GLL024 Gallbladder Disease 1 53 0.025
574
GLL028 Gillespie Syndrome 53 0.025
575
CHR073 Choreatic Disease 52 0.025
576
PRP016 Paraplegia 52 0.025
577
c VRL010 Viral Hepatitis 52 0.025
578
IMP005 Impotence 52 0.025
579
ART140 Arteries, Anomalies of 52 0.025
580
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 52 0.025
581
BWN001 Bowen-Conradi Syndrome 52 0.025
582
FML037 Female Breast Cancer 52 0.025
583
PTH003 Pathologic Nystagmus 52 0.025
584
c ACT135 Acute Graft Versus Host Disease 52 0.025
585
P TRT010 Teratoma 52 0.025
586
PRV004 Periventricular Leukomalacia 52 0.025
587
P SPP010 Suppressor of Tumorigenicity 3 51 0.025
588
ILS001 Ileus 51 0.025
589
c PRM108 Primary Progressive Multiple Sclerosis 51 0.025
590
P PRC012 Pericardial Effusion 51 0.025
591
FBR008 Fibrillary Astrocytoma 51 0.025
592
TNG007 Tongue Carcinoma 51 0.025
593
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.025
594
HYP781 Hypoascorbemia 51 0.025
595
SCH012 Schizoaffective Disorder 50 0.025
596
SPN021 Spinal Meningioma 50 0.025
597
CRT013 Carotid Stenosis 50 0.025
598
c HRD202 Hereditary Lymphedema I 50 0.025
599
PRT018 Portal Vein Thrombosis 50 0.025
600
VTR016 Vater/vacterl Association 50 0.025
601
PRN009 Paranoid Schizophrenia 50 0.025
602
DBT004 Diabetic Polyneuropathy 49 0.025
603
SYS003 Systolic Heart Failure 49 0.025
604
HDR003 Hidradenitis 49 0.025
605
PRS129 Prostatic Hyperplasia, Benign 49 0.025
606
DYS009 Dysthymic Disorder 49 0.025
607
URM002 Uremia 49 0.025
608
P BRS053 Breast Fibroadenoma 49 0.025
609
VCC001 Vaccinia 49 0.025
610
VTM033 Vitamin K Deficiency Bleeding 48 0.025
611
CLS016 Clostridium Difficile Colitis 48 0.025
612
BBS001 Babesiosis 48 0.025
613
IGG001 Iga Glomerulonephritis 48 0.025
614
HMP001 Hemopericardium 48 0.025
615
HYP025 Hyperphosphatemia 48 0.025
616
c PRM226 Primary Central Nervous System Lymphoma 48 0.025
617
DRG003 Drug Dependence 47 0.025
618
CLF056 Cleft Lip with or Without Cleft Palate 47 0.025
619
ANH002 Anhidrosis 47 0.025
620
ACT084 Acute Stress Disorder 47 0.025
621
SRT004 Serotonin Syndrome 47 0.025
622
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.025
623
P PRC019 Precocious Puberty 46 0.025
624
RTN023 Retinitis 46 0.025
625
ATN005 Autonomic Dysfunction 46 0.025
626
TTH006 Tooth Disease 46 0.025
627
SMT001 Somatization Disorder 46 0.025
628
c GRN049 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I 46 0.025
629
P PNT019 Pontocerebellar Hypoplasia 46 0.025
630
TCL003 T Cell Deficiency 46 0.025
631
c MLG068 Malignant Glioma 46 0.025
632
c LFR007 Li-Fraumeni Syndrome 2 45 0.025
633
URL001 Urolithiasis 45 0.025
634
GLC036 Glucagonoma 45 0.025
635
ATN004 Autonomic Neuropathy 45 0.025
636
DBT008 Diabetic Angiopathy 44 0.025
637
DWR001 Dwarfism 44 0.025
638
SCH030 Schneckenbecken Dysplasia 44 0.025
639
CRB027 Cerebellar Disease 44 0.025
640
c HYP272 Hypercholesterolemia, Familial, 3 44 0.025
641
CRB090 Cerebral Hypoxia 44 0.025
642
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.025
643
c MLG147 Malignant Hyperthermia 1 43 0.025
644
MYX004 Myxedema 43 0.025
645
LWC001 Low Compliance Bladder 43 0.025
646
MYC013 Mycobacterium Abscessus 43 0.025
647
P HYP265 Hypotonia 43 0.025
648
PMP004 Pemphigus Foliaceus 43 0.025
649
MST004 Mast Cell Neoplasm 42 0.025
650
BNS003 Binswanger's Disease 42 0.025
651
MRS001 Marasmus 42 0.025
652
CRN285 Corneal Dystrophy, Fleck 42 0.025
653
ATX019 Ataxia with Vitamin E Deficiency 42 0.025
654
BNB002 Bainbridge-Ropers Syndrome 42 0.025
655
SPN050 Spinocerebellar Degeneration 42 0.025
656
NRR001 Neuroretinitis 42 0.025
657
EHR002 Ehrlichiosis 42 0.025
658
MMM006 Mammographic Density 41 0.025
659
DBT002 Diabetic Autonomic Neuropathy 41 0.025
660
P RRH023 Rare Hereditary Hemochromatosis 41 0.025
661
P CRB045 Cerebellar Hypoplasia 41 0.025
662
LRG008 Large Granular Lymphocyte Leukemia 41 0.025
663
SCR001 Secretory Meningioma 41 0.025
664
P RRT020 Rare Tumor 41 0.025
665
MRP001 Morphine Dependence 41 0.025
666
ADS004 Aids Dementia Complex 40 0.025
667
SKL017 Skeletal Dysplasias 40 0.025
668
P TRC031 Trichorhinophalangeal Syndrome 40 0.025
669
ART008 Arteriosclerosis Obliterans 40 0.025
670
CHL045 Choline Deficiency Disease 39 0.025
671
LNG030 Lung Adenoma 39 0.025
672
LKP003 Leukoplakia 39 0.025
673
WLL004 Wallerian Degeneration 39 0.025
674
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.025
675
NRD004 Neurodegeneration Due to Cerebral Folate Transport Deficiency 39 0.025
676
SCR011 Scrapie 39 0.025
677
EXT007 Extracutaneous Mastocytoma 38 0.025
678
OVR094 Ovarian Epithelial Cancer 38 0.025
679
ATX023 Ataxia, Sensory, 1, Autosomal Dominant 38 0.025
680
c HNT011 Huntington Disease-Like 3 38 0.025
681
P FML187 Familial Hypertension 37 0.025
682
GLM044 Glomerular Disease 37 0.025
683
P CRB059 Cerebellar Degeneration 37 0.025
684
c CHR020 Chronic Interstitial Cystitis 37 0.025
685
HMM004 Hamamy Syndrome 37 0.025
686
BRR002 Barrett's Adenocarcinoma 36 0.025
687
c HMG004 Hemoglobin D Disease 36 0.025
688
PLC002 Plica Syndrome 36 0.025
689
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.025
690
c VRL004 Viral Labyrinthitis 35 0.025
691
CLD011 Cold Urticaria 35 0.025
692
HNS001 Hansen's Disease 34 0.025
693
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.025
694
c PRG106 Progressive Muscular Dystrophy 33 0.025
695
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 33 0.025
696
HND015 Hand Skill, Relative 33 0.025
697
P GLY112 Glycosylphosphatidylinositol Biosynthesis Defect 1 32 0.025
698
c SCH080 Schizophrenia 3 32 0.025
699
OVR109 Ovarian Germ Cell Teratoma 32 0.025
700
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 30 0.025
701
CVR010 Cavernous Malformation 30 0.025
702
c DFN253 Deafness, Autosomal Recessive 84a 30 0.025
703
CRD220 Cardiac Valvular Defect, Developmental 29 0.025
704
TRT017 Teratoma, Ovarian 29 0.025
705
TCK004 Tick Infestation 28 0.025
706
CHN045 Chondrodysplasia with Joint Dislocations, Gpapp Type 28 0.025
707
ACT162 Acute Sensory Ataxic Neuropathy 26 0.025
708
MLG164 Malignant Epithelial Tumor of Ovary 26 0.025
709
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.025
710
NNT021 Neonatal Meningitis 25 0.025
711
LBR035 Liberfarb Syndrome 24 0.025
712
c ALZ053 Alzheimer Disease 7 24 0.025
713
APN006 Apnea of Prematurity 24 0.025
714
c TYP027 Type 1 Diabetes Mellitus 10 21 0.025
715
CGT001 Ciguatera Fish Poisoning 20 0.025
716
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 17 0.025
717
c MNT281 Mental Retardation, Autosomal Recessive 59 17 0.025
718
c RNL034 Renal Cell Carcinoma 4 16 0.025
719
PNF002 Painful Legs and Moving Toes Syndrome 14 0.025
720
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.025
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