Search results for Riboflavin

663 hits were found for Riboflavin

# Family MCID Name MIFTS Score
1
RBF001 Riboflavin Deficiency 49 9.408
2
FZL002 Fazio-Londe Disease 44 5.391
3
EXR006 Exercise Intolerance, Riboflavin-Responsive 16 4.712
4
c BRW008 Brown-Vialetto-Van Laere Syndrome 2 35 3.423
5
c BRW009 Brown-Vialetto-Van Laere Syndrome 1 37 3.332
6
P BRW001 Brown-Vialetto-Van Laere Syndrome 33 2.637
7
P KRT007 Keratoconus 50 0.424
8
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.206
9
KRT019 Keratitis, Hereditary 65 0.206
10
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.172
11
c MGR028 Migraine with or Without Aura 1 67 0.169
12
P MYP004 Myopathy 70 0.165
13
CRN009 Corneal Ectasia 28 0.165
14
P CRN024 Corneal Disease 44 0.150
15
IRN002 Iron Metabolism Disease 57 0.145
16
AST006 Astigmatism 47 0.145
17
P MYP006 Myopia 55 0.128
18
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.128
19
MSC193 Muscular Lipidosis 23 0.125
20
P LCT001 Lactic Acidosis 51 0.115
21
P NRP001 Neuropathy 56 0.111
22
P LVR013 Liver Disease 68 0.104
23
P CTR002 Cataract 60 0.104
24
STM007 Stomatitis 50 0.104
25
ESP021 Esophageal Cancer 90 0.100
26
ALC007 Alcohol Dependence 66 0.100
27
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.100
28
FTT001 Fatty Liver Disease 61 0.096
29
OCL069 Ocular Motor Apraxia 51 0.096
30
P CRN026 Corneal Edema 43 0.096
31
PYR016 Pyridoxine Deficiency 30 0.096
32
BLR008 Bilirubin Metabolic Disorder 57 0.092
33
P TRN020 Turner Syndrome 67 0.088
34
HYP056 Hypoglycemia 66 0.088
35
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.088
36
SKN016 Skin Disease 63 0.088
37
c BRN108 Branchiootic Syndrome 1 62 0.088
38
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.088
39
P HDC001 Headache 57 0.088
40
IRR001 Irregular Astigmatism 30 0.088
41
DFC004 Deficiency Anemia 70 0.084
42
P SNS001 Sensorineural Hearing Loss 60 0.084
43
EYD002 Eye Disease 58 0.084
44
P CRN028 Corneal Ulcer 47 0.084
45
KWS001 Kwashiorkor 44 0.084
46
RFR003 Refractive Error 43 0.084
47
MLR004 Malaria 81 0.079
48
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.079
49
P PRP019 Peripheral Nervous System Disease 58 0.079
50
BLL004 Bullous Keratopathy 49 0.079
51
KRT008 Keratopathy 47 0.079
52
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.074
53
P PSR002 Psoriasis 62 0.074
54
SQM006 Squamous Cell Carcinoma 60 0.074
55
PST011 Pustulosis of Palm and Sole 52 0.074
56
DYS073 Dysphagia 50 0.074
57
P BRB001 Beriberi 46 0.074
58
PLL009 Pellucid Marginal Degeneration 22 0.074
59
P BRS047 Breast Cancer 97 0.068
60
STR067 Stroke, Ischemic 81 0.068
61
P RSP003 Respiratory Failure 74 0.068
62
P GRF003 Graft-Versus-Host Disease 72 0.068
63
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.068
64
c PRC016 Pre-Eclampsia 63 0.068
65
HMC014 Homocysteinemia 53 0.068
66
NNT012 Neonatal Jaundice 53 0.068
67
c INH020 Inherited Metabolic Disorder 47 0.068
68
P HYP265 Hypotonia 43 0.068
69
PPL052 Papillomatosis, Confluent and Reticulated 33 0.068
70
P HPT023 Hepatocellular Carcinoma 100 0.062
71
CRV035 Cervical Cancer 76 0.062
72
P HYP086 Hypothyroidism 69 0.062
73
CRB039 Cerebrovascular Disease 67 0.062
74
c RHB024 Rhabdomyosarcoma 2 67 0.062
75
P MTR014 Motor Neuron Disease 65 0.062
76
LVR012 Liver Cirrhosis 62 0.062
77
NTR005 Nutritional Deficiency Disease 62 0.062
78
CHL014 Cholera 59 0.062
79
ISC004 Ischemia 58 0.062
80
BCT022 Bacterial Infectious Disease 56 0.062
81
DYS015 Dysentery 52 0.062
82
HLX001 Helix Syndrome 47 0.062
83
GLS007 Glossitis 47 0.062
84
MRS001 Marasmus 42 0.062
85
FNG016 Fungal Keratitis 40 0.062
86
CRN022 Corneal Degeneration 36 0.062
87
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.062
88
ACN019 Acanthamoeba Keratitis 31 0.062
89
ANG061 Angular Cheilitis 26 0.062
90
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.056
91
CRH001 Crohn's Disease 74 0.056
92
DWN001 Down Syndrome 70 0.056
93
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.056
94
P MLN008 Melanoma 69 0.056
95
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.056
96
ATH013 Atherosclerosis Susceptibility 65 0.056
97
P DBT009 Diabetes Mellitus 64 0.056
98
CLF027 Cleft Palate, Isolated 64 0.056
99
ANR007 Anorexia Nervosa 63 0.056
100
BLL006 Bullous Pemphigoid 62 0.056
101
ATM095 Autoimmune Disease 62 0.056
102
HYP066 Hyperglycemia 61 0.056
103
P ENC018 Encephalopathy 61 0.056
104
DPH001 Diphtheria 60 0.056
105
IRN001 Iron Deficiency Anemia 59 0.056
106
P ALC033 Alcohol Use Disorder 58 0.056
107
HYP266 Hypoxia 57 0.056
108
P PLY019 Polyneuropathy 56 0.056
109
P DRR001 Diarrhea 55 0.056
110
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.056
111
PRT038 Protein-Energy Malnutrition 54 0.056
112
P INF037 Inflammatory Bowel Disease 54 0.056
113
ABL002 Ablepharon-Macrostomia Syndrome 53 0.056
114
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 53 0.056
115
RYS001 Reye Syndrome 51 0.056
116
MTB004 Metabolic Acidosis 50 0.056
117
P MTC133 Mitochondrial Myopathy 49 0.056
118
ATS010 Autosomal Recessive Disease 48 0.056
119
KRT002 Keratomalacia 47 0.056
120
P MTH007 Methemoglobinemia 46 0.056
121
EPD015 Epidemic Typhus 45 0.056
122
HMP009 Haemophilus Influenzae 43 0.056
123
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.056
124
FRS019 Farsightedness 38 0.056
125
ATM052 Autoimmune Disease 1 37 0.056
126
P ADT009 Auditory Neuropathy Spectrum Disorder 36 0.056
127
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.056
128
LPD042 Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency 21 0.056
129
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.048
130
c SYS001 Systemic Lupus Erythematosus 86 0.048
131
c HYP595 Hypertension, Essential 84 0.048
132
P HRT032 Heart Disease 75 0.048
133
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.048
134
ANX010 Anxiety 73 0.048
135
P KDN018 Kidney Disease 72 0.048
136
P MLT020 Multiple Sclerosis 72 0.048
137
PLM001 Pulmonary Tuberculosis 69 0.048
138
SVR097 Severe Cutaneous Adverse Reaction 69 0.048
139
P MYC084 Mycobacterium Tuberculosis 1 68 0.048
140
CNN005 Connective Tissue Disease 68 0.048
141
c INF071 Inflammatory Bowel Disease 1 67 0.048
142
CRP001 Carpal Tunnel Syndrome 67 0.048
143
CHG001 Chagas Disease 66 0.048
144
P CNJ013 Conjunctivitis 65 0.048
145
P HRP006 Herpes Simplex 65 0.048
146
PRT036 Peritonitis 64 0.048
147
BRC012 Brucellosis 64 0.048
148
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.048
149
PLM031 Poliomyelitis 64 0.048
150
LSH001 Leishmaniasis 63 0.048
151
P ESP024 Esophagitis 62 0.048
152
c PNS012 Paine Syndrome 61 0.048
153
P LPS004 Lupus Erythematosus 61 0.048
154
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.048
155
P BRS044 Breast Adenocarcinoma 59 0.048
156
P SYP003 Syphilis 58 0.048
157
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.048
158
ERY003 Erythema Multiforme 58 0.048
159
P EHL001 Ehlers-Danlos Syndrome 58 0.048
160
P PLV020 Pelvic Organ Prolapse 57 0.048
161
P PLY041 Polymyositis 57 0.048
162
P CRD246 Cardiovascular System Disease 57 0.048
163
GLT035 Glutaric Acidemia I 57 0.048
164
MCS002 Mucositis 56 0.048
165
OCL020 Ocular Cicatricial Pemphigoid 55 0.048
166
P HYP076 Hyperthyroidism 55 0.048
167
P LTR001 Lateral Sclerosis 54 0.048
168
PPL022 Papilloma 54 0.048
169
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.048
170
CRH005 Crohn's Colitis 53 0.048
171
c PSR017 Psoriasis 2 53 0.048
172
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.048
173
DMY004 Demyelinating Disease 52 0.048
174
c PSR023 Psoriasis 1 52 0.048
175
CCT002 Cicatricial Pemphigoid 51 0.048
176
c EHL078 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 51 0.048
177
HYP781 Hypoascorbemia 51 0.048
178
P BRT029 Brittle Cornea Syndrome 2 50 0.048
179
P SCK005 Sickle Cell Disease 50 0.048
180
ADR038 Adermatoglyphia 49 0.048
181
c DSB006 Desbuquois Dysplasia 1 48 0.048
182
c PSR032 Psoriasis 11 47 0.048
183
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.048
184
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.048
185
SQM002 Squamous Cell Papilloma 46 0.048
186
ORG002 Organic Acidemia 44 0.048
187
DWR001 Dwarfism 44 0.048
188
c PSR028 Psoriasis 7 42 0.048
189
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.048
190
P KLZ004 Kala-Azar 1 41 0.048
191
c PSR018 Psoriasis 13 41 0.048
192
ANX004 Anoxia 40 0.048
193
CHL045 Choline Deficiency Disease 39 0.048
194
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.048
195
c SYS043 Systemic Lupus Erythematosus 1 38 0.048
196
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.048
197
ERY066 Erythema Multiforme Major 30 0.048
198
GLT028 Glutaric Aciduria Iii 27 0.048
200
SPR019 Superficial Keratitis 21 0.048
201
P CLR023 Colorectal Cancer 99 0.039
202
P LNG032 Lung Cancer 98 0.039
203
P PRS040 Prostate Cancer 97 0.039
204
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.039
205
P GST053 Gastric Cancer 83 0.039
206
NRL016 Neural Tube Defects 82 0.039
207
CYS001 Cystic Fibrosis 81 0.039
208
P RHM011 Rheumatoid Arthritis 80 0.039
209
c NRF023 Neurofibromatosis, Type Ii 80 0.039
210
P PRK057 Parkinson Disease, Late-Onset 78 0.039
211
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.039
212
c ATR087 Atrial Standstill 1 75 0.039
213
P OST002 Osteoporosis 74 0.039
214
HMN044 Human Immunodeficiency Virus Type 1 71 0.039
215
P MYC007 Myocardial Infarction 70 0.039
216
CNG034 Congestive Heart Failure 69 0.039
217
P ART022 Arthritis 69 0.039
218
SKN019 Skin Melanoma 68 0.039
219
RCK004 Rickets 68 0.039
220
P HPT021 Hepatitis 67 0.039
221
P MNN013 Meningitis 66 0.039
222
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.039
223
P PRD008 Periodontitis 64 0.039
224
OST017 Osteomyelitis 64 0.039
225
P HML002 Hemolytic Anemia 63 0.039
226
P ANR048 Aniridia 1 63 0.039
227
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.039
228
P VSC007 Vascular Disease 63 0.039
229
P CRN300 Coronary Heart Disease 1 63 0.039
230
DPR016 Depression 63 0.039
231
LPD008 Lipid Metabolism Disorder 62 0.039
232
CLT003 Colitis 62 0.039
233
c HPT003 Hepatitis a 62 0.039
234
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.039
235
c SVR001 Severe Acute Respiratory Syndrome 62 0.039
236
LPP008 Lipoprotein Quantitative Trait Locus 62 0.039
237
P HYP750 Hypertriglyceridemia, Familial 62 0.039
238
ALL026 Allergic Hypersensitivity Disease 62 0.039
239
MSL001 Measles 62 0.039
240
P PRP029 Porphyria 62 0.039
241
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.039
242
P ENC004 Encephalitis 61 0.039
243
P PNC044 Pancreatitis 61 0.039
244
c ACT027 Acute Pancreatitis 60 0.039
245
ACN002 Acanthosis Nigricans 60 0.039
246
ACQ007 Acquired Immunodeficiency Syndrome 60 0.039
247
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 0.039
248
c HPT016 Hepatitis B 59 0.039
249
P LKD001 Leukodystrophy 59 0.039
250
ADN018 Adenoma 59 0.039
251
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.039
252
FBR047 Fibromyalgia 58 0.039
253
SPT004 Septic Arthritis 58 0.039
254
BRS051 Breast Disease 58 0.039
255
CRV038 Cervical Squamous Cell Carcinoma 58 0.039
256
MNT002 Mental Depression 58 0.039
257
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.039
258
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.039
259
APH001 Aphthous Stomatitis 57 0.039
260
JPN002 Japanese Encephalitis 57 0.039
261
SLC006 Silicosis 56 0.039
262
AGN016 Aging 56 0.039
263
c FML035 Familial Hyperlipidemia 55 0.039
264
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.039
265
RSC001 Rosacea 54 0.039
266
MTC020 Mitochondrial Complex Ii Deficiency 54 0.039
267
THR013 Thoracic Outlet Syndrome 54 0.039
268
P TRM003 Tremor 54 0.039
269
P RTN016 Retinal Degeneration 53 0.039
270
GST023 Gastric Ulcer 53 0.039
271
c VRL010 Viral Hepatitis 52 0.039
272
ACR041 Acromelic Frontonasal Dysostosis 52 0.039
273
PLS007 Plasmodium Falciparum Malaria 52 0.039
274
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.039
275
P MGR003 Migraine with Aura 52 0.039
276
KRT009 Keratosis 51 0.039
277
END086 End Stage Renal Disease 51 0.039
278
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.039
279
BLP005 Blepharitis 50 0.039
280
PLC008 Placenta Disease 50 0.039
281
P MGR001 Migraine Without Aura 49 0.039
282
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.039
283
TBR011 Tuberculous Meningitis 48 0.039
284
P PRR002 Pure Red-Cell Aplasia 47 0.039
285
LYM019 Lymphosarcoma 46 0.039
286
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.039
287
P TRM004 Trimethylaminuria 46 0.039
288
P PLL002 Pellagra 46 0.039
289
c DRR009 Diarrhea 6 46 0.039
290
TRT001 Teratocarcinoma 45 0.039
291
CRB004 Cerebral Artery Occlusion 45 0.039
292
SBC016 Subacute Delirium 44 0.039
293
GRN017 Granulocytopenia 44 0.039
294
P MTC004 Mitochondrial Encephalomyopathy 44 0.039
295
CVD001 Covid-19 44 0.039
296
P DMY001 Demyelinating Polyneuropathy 43 0.039
297
MDD018 Middle East Respiratory Syndrome 43 0.039
298
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.039
299
SNL007 Senile Cataract 42 0.039
300
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.039
301
ATX019 Ataxia with Vitamin E Deficiency 42 0.039
302
CRV045 Cervical Intraepithelial Neoplasia 39 0.039
303
48X005 48,xyyy 39 0.039
304
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.039
305
GRN055 Granular Corneal Dystrophy 36 0.039
306
P AXN001 Axonal Neuropathy 36 0.039
307
MTC151 Mitochondrial Complex I Deficiency, Nuclear Type 20 35 0.039
308
ATX010 Ataxia Neuropathy Spectrum 34 0.039
309
PYR009 Pyridoxine Deficiency Anemia 34 0.039
310
PRG007 Progressive Bulbar Palsy 34 0.039
311
ACT064 Acute Necrotizing Encephalitis 33 0.039
312
c KRT029 Keratoconus 1 33 0.039
313
CHR696 Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia 32 0.039
314
DGN002 Degenerative Myopia 32 0.039
315
EXN003 Exencephaly 31 0.039
316
PLR005 Pleuropneumonia 31 0.039
317
PLM049 Plummer Vinson Syndrome 30 0.039
318
MDR004 Madras Motor Neuron Disease 29 0.039
319
PTT016 Patterson Pseudoleprechaunism Syndrome 28 0.039
320
END014 Endemic Typhus 27 0.039
321
CHL079 Children's Interstitial Lung Disease 26 0.039
322
c PRM209 Primary Trimethylaminuria 18 0.039
323
BLD137 Blood Group--Ahonen 16 0.039
324
c PHT009 Photoparoxysmal Response 2 14 0.039
325
P OVR042 Ovarian Cancer 88 0.028
326
P ATX030 Ataxia-Telangiectasia 82 0.028
327
P BLD134 Bladder Cancer 79 0.028
328
PHN003 Phenylketonuria 75 0.028
329
END057 Endometrial Cancer 74 0.028
330
SCK003 Sickle Cell Anemia 74 0.028
331
P SCH015 Schizophrenia 74 0.028
332
SVR004 Severe Combined Immunodeficiency 73 0.028
333
c HYP836 Hypercholesterolemia, Familial, 1 73 0.028
334
ULC004 Ulcerative Colitis 73 0.028
335
c SPN225 Spondyloarthropathy 1 73 0.028
336
P CNR004 Cone-Rod Dystrophy 2 73 0.028
337
P RTN024 Retinoblastoma 73 0.028
338
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.028
339
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.028
340
c HPT073 Hepatitis C Virus 72 0.028
341
P NRB001 Neuroblastoma 72 0.028
342
PRP027 Peripheral Vascular Disease 71 0.028
343
P SRC025 Sarcoidosis 1 70 0.028
344
MLT157 Multiple System Atrophy 1 70 0.028
345
LGH007 Leigh Syndrome 70 0.028
346
P HYP061 Hypertrophic Cardiomyopathy 70 0.028
347
c CHR684 Chronic Kidney Disease 70 0.028
348
ADL002 Adult Syndrome 70 0.028
349
P ASP006 Aspergillosis 69 0.028
350
CRB037 Cerebral Palsy 69 0.028
351
P SLP006 Sleep Apnea 69 0.028
352
P OCL013 Oculodentodigital Dysplasia 69 0.028
353
ART016 Aortic Aneurysm 69 0.028
354
P ANG001 Angelman Syndrome 69 0.028
355
P LKM062 Leukemia, Acute Lymphoblastic 69 0.028
356
P LYM118 Lymphoma 68 0.028
357
P PNM007 Pneumonia 68 0.028
358
BRN024 Bronchitis 68 0.028
359
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.028
360
P THR014 Thrombocytopenia 67 0.028
361
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.028
362
c FML021 Familial Hypercholesterolemia 66 0.028
363
P SKN015 Skin Carcinoma 66 0.028
364
P MCR115 Microvascular Complications of Diabetes 5 66 0.028
365
ART001 Arterial Tortuosity Syndrome 66 0.028
366
AND002 Androgen Insensitivity Syndrome 66 0.028
367
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.028
368
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.028
369
P DYS154 Dystonia 65 0.028
370
PPL049 Papillon-Lefevre Syndrome 65 0.028
371
BRR014 Barrett Esophagus 65 0.028
372
PND002 Pendred Syndrome 65 0.028
373
PRT037 Pertussis 65 0.028
374
P PRS038 Personality Disorder 65 0.028
375
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.028
376
CLN015 Colon Adenocarcinoma 65 0.028
377
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.028
378
P CHR071 Charcot-Marie-Tooth Disease 65 0.028
379
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.028
380
CLR108 Colorectal Adenoma 64 0.028
381
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.028
382
c CNG006 Congenital Hypothyroidism 64 0.028
383
P ADN016 Adenocarcinoma 64 0.028
384
P FTL069 Fetal Akinesia Deformation Sequence 1 64 0.028
385
KRN002 Kearns-Sayre Syndrome 63 0.028
386
P GLM045 Glioma 63 0.028
387
TYP007 Typhoid Fever 63 0.028
388
c ACT068 Acute Cystitis 63 0.028
389
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.028
390
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.028
391
c FNC043 Fanconi Anemia, Complementation Group E 62 0.028
392
c HPT001 Hepatitis C 62 0.028
393
P TRC086 Trichohepatoenteric Syndrome 1 62 0.028
394
HYD038 Hydrops Fetalis, Nonimmune 62 0.028
395
P ACR001 Aicardi-Goutieres Syndrome 62 0.028
396
CRN239 Carnitine Deficiency, Systemic Primary 62 0.028
397
MDD011 Mood Disorder 62 0.028
398
P PRM006 Primary Biliary Cirrhosis 62 0.028
399
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.028
400
ALC006 Alcoholic Hepatitis 61 0.028
401
RTN017 Retinal Detachment 61 0.028
402
SDD001 Sudden Infant Death Syndrome 61 0.028
403
P KDN017 Kidney Cancer 60 0.028
404
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.028
405
P SCL018 Scoliosis 60 0.028
406
P VNT002 Ventricular Septal Defect 60 0.028
407
ORL011 Oral Cancer 60 0.028
408
INS001 Insulinoma 60 0.028
409
ETN001 Eating Disorder 60 0.028
410
c ACT071 Acute Kidney Failure 60 0.028
411
NRF008 Neurofibromatosis-Noonan Syndrome 60 0.028
412
P HRD011 Hereditary Spherocytosis 60 0.028
413
P MYC008 Myocarditis 59 0.028
414
P AXN002 Axenfeld-Rieger Syndrome 59 0.028
415
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.028
416
P SLP005 Sleep Disorder 59 0.028
417
GNG013 Gingivitis 59 0.028
418
P DNG005 Dengue Virus 59 0.028
419
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.028
420
HLC007 Helicobacter Pylori Infection 59 0.028
421
ANR040 Aneurysm 59 0.028
422
PPT005 Peptic Ulcer Disease 59 0.028
423
P ANP001 Anaplastic Large Cell Lymphoma 58 0.028
424
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.028
425
PST028 Post-Traumatic Stress Disorder 58 0.028
426
CMP010 Complex Regional Pain Syndrome 58 0.028
427
SCR008 Scrub Typhus 58 0.028
428
DSS008 Disease of Mental Health 58 0.028
429
CNS004 Constipation 58 0.028
430
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.028
431
P INF032 Infertility 57 0.028
432
GLS018 Glass Syndrome 57 0.028
433
c CHR417 Chronic Graft Versus Host Disease 57 0.028
434
CHL067 Cholecystitis 57 0.028
435
THR024 Thrombosis 57 0.028
436
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.028
437
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.028
438
AYM001 Ayme-Gripp Syndrome 57 0.028
439
PNM008 Pneumothorax 56 0.028
440
CMR002 Coumarin Resistance 56 0.028
441
LST001 Listeriosis 56 0.028
442
LMY014 Leiomyoma, Uterine 56 0.028
443
P MTC069 Mitochondrial Disorders 56 0.028
444
HMG005 Hemoglobinopathy 56 0.028
445
PPL025 Popliteal Pterygium Syndrome 56 0.028
446
GST050 Gastrointestinal System Disease 56 0.028
447
BRN004 Brain Edema 56 0.028
448
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 55 0.028
449
HYP005 Hypokalemia 55 0.028
450
ICH001 Ichthyosis Vulgaris 55 0.028
451
P MLN007 Male Infertility 55 0.028
452
VSC003 Visceral Leishmaniasis 55 0.028
453
ISV001 Isovaleric Acidemia 55 0.028
454
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 55 0.028
455
P ANT006 Antiphospholipid Syndrome 55 0.028
456
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.028
457
P GRV001 Graves' Disease 55 0.028
458
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.028
459
RNL051 Renal Cysts and Diabetes Syndrome 55 0.028
460
P SBS003 Substance Abuse 55 0.028
461
P ALP106 Alport Syndrome 1, X-Linked 55 0.028
462
BRN045 Brunner Syndrome 55 0.028
463
END040 Endogenous Depression 55 0.028
464
P LRY044 Larynx Cancer 55 0.028
465
ACD008 Acid-Labile Subunit Deficiency 54 0.028
466
PLM010 Pulmonary Edema 54 0.028
467
P ART021 Arteriosclerosis 54 0.028
468
AMN001 Amenorrhea 54 0.028
469
DBT010 Diabetic Neuropathy 54 0.028
470
HMS001 Hemosiderosis 54 0.028
471
WST005 West Nile Virus 54 0.028
472
SNS003 Sensory Peripheral Neuropathy 54 0.028
473
SLP001 Sleeping Sickness 54 0.028
474
PNC001 Pancytopenia 54 0.028
475
CLR030 Clear Cell Renal Cell Carcinoma 53 0.028
476
PLM012 Pulmonary Sarcoidosis 53 0.028
477
TRC023 Trichinosis 53 0.028
478
RHM028 Rheumatic Heart Disease 53 0.028
479
P HMC002 Homocystinuria 53 0.028
480
ENC055 Encephalopathy, Ethylmalonic 53 0.028
481
GTR002 Goiter 53 0.028
482
P PTS002 Ptosis 53 0.028
483
c HPT007 Hepatitis E 53 0.028
484
c FML008 Familial Retinoblastoma 53 0.028
485
c CNT035 Central Nervous System Disease 52 0.028
486
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.028
487
DRM011 Dermatophytosis 52 0.028
488
ESP023 Esophageal Disease 52 0.028
489
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.028
490
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.028
491
P RCT021 Rectum Cancer 52 0.028
492
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.028
493
ART140 Arteries, Anomalies of 52 0.028
494
P NRC002 Narcolepsy 52 0.028
495
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.028
496
P THY032 Thyroiditis 52 0.028
497
BWN001 Bowen-Conradi Syndrome 52 0.028
498
PTH003 Pathologic Nystagmus 52 0.028
499
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.028
500
LMY002 Leiomyoma 52 0.028
501
SPS003 Spastic Diplegia 51 0.028
502
LYM004 Lymphoid Interstitial Pneumonia 51 0.028
503
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.028
504
FDL002 Food Allergy 51 0.028
505
FMR004 Fumarase Deficiency 51 0.028
506
MGL001 Megaloblastic Anemia 51 0.028
507
c PRM108 Primary Progressive Multiple Sclerosis 51 0.028
508
c PRK086 Parkinson Disease 15, Autosomal Recessive Early-Onset 51 0.028
509
TRM010 Traumatic Brain Injury 51 0.028
510
P THR015 Thrombophilia 51 0.028
511
SKN013 Skin Benign Neoplasm 51 0.028
512
HYP081 Hypolipoproteinemia 51 0.028
513
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.028
514
P OVR082 Overgrowth Syndrome 50 0.028
515
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.028
516
c SVR005 Severe Pre-Eclampsia 50 0.028
517
ASC010 Ascaris Lumbricoides Infection 50 0.028
518
PLM017 Pulmonary Alveolar Microlithiasis 50 0.028
519
NTR046 Neutrophil Migration 50 0.028
520
OPT003 Opiate Dependence 50 0.028
521
ENT004 Enthesopathy 49 0.028
522
P CRV039 Cervicitis 49 0.028
523
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.028
524
CCN002 Cocaine Abuse 49 0.028
525
47X002 47,xyy 49 0.028
526
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.028
527
BRN071 Brain Injury 49 0.028
528
URM002 Uremia 49 0.028
529
c INV001 Invasive Aspergillosis 49 0.028
530
EBL001 Ebola Hemorrhagic Fever 49 0.028
531
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.028
532
CCN001 Cocaine Dependence 48 0.028
533
P NGH001 Night Blindness 48 0.028
534
VTM033 Vitamin K Deficiency Bleeding 48 0.028
535
SPL018 Splenomegaly 48 0.028
536
P SCL015 Scleritis 48 0.028
537
c MTR002 Mitral Valve Insufficiency 48 0.028
538
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.028
539
HPR003 Heparin-Induced Thrombocytopenia 48 0.028
540
DRG003 Drug Dependence 47 0.028
541
VRN004 Vernal Keratoconjunctivitis 47 0.028
542
CRN027 Corneal Neovascularization 47 0.028
543
WRN003 Wernicke Encephalopathy 47 0.028
544
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.028
545
ANV001 Anovulation 47 0.028
546
CNZ001 Coenzyme Q10 Deficiency Disease 47 0.028
547
CRD137 Cardiogenic Shock 47 0.028
548
CHR074 Choriocarcinoma 47 0.028
549
CYC008 Cyclic Vomiting Syndrome 47 0.028
550
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.028
551
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.028
552
TNP001 Tinea Pedis 46 0.028
553
TTH006 Tooth Disease 46 0.028
554
c GLC111 Galactosemia Ii 46 0.028
555
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.028
556
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.028
557
P MYC033 Myoclonus 46 0.028
558
OPD001 Opioid Abuse 46 0.028
559
GLL048 Glial Tumor 45 0.028
560
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.028
561
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.028
562
ESP027 Esophagus Squamous Cell Carcinoma 45 0.028
563
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 45 0.028
564
c HMG003 Hemoglobin E Disease 45 0.028
565
MYF001 Myofibroma 45 0.028
566
P CHR345 Chronic Pain 44 0.028
567
IRT001 Iritis 44 0.028
568
CNN002 Cannabis Abuse 44 0.028
569
FCH001 Fuchs' Endothelial Dystrophy 44 0.028
570
P ORF002 Orofacial Cleft 44 0.028
571
P HYP111 Hyperprolinemia 44 0.028
572
EGG001 Egg Allergy 44 0.028
573
c HYP272 Hypercholesterolemia, Familial, 3 44 0.028
574
c SPH013 Spherocytosis, Type 1 44 0.028
575
INT258 Interstitial Nephritis, Karyomegalic 44 0.028
576
c PRM038 Primary Agammaglobulinemia 44 0.028
577
HPT082 Hepatic Adenomas, Familial 44 0.028
578
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.028
579
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.028
580
RDC006 Red Cell Aplasia 43 0.028
581
HYP084 Hypopyon 43 0.028
582
c SRC023 Sarcoidosis 2 43 0.028
583
PLY068 Polysubstance Abuse 43 0.028
584
TRP009 Triple X Syndrome 42 0.028
585
CYT002 Cytokine Deficiency 42 0.028
586
P CRN035 Cranial Nerve Palsy 42 0.028
588
LMR001 Lemierre's Syndrome 42 0.028
589
MYF002 Myofascial Pain Syndrome 42 0.028
590
MMM006 Mammographic Density 41 0.028
591
DBT002 Diabetic Autonomic Neuropathy 41 0.028
592
PRS063 Paresthesia 41 0.028
593
P RRH023 Rare Hereditary Hemochromatosis 41 0.028
594
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 40 0.028
595
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.028
596
HPR006 Heparin Cofactor Ii Deficiency 40 0.028
597
CLD014 Cole Disease 40 0.028
598
P PRG092 Pregnancy Loss, Recurrent 1 40 0.028
599
CNN001 Cannabis Dependence 40 0.028
600
LKP003 Leukoplakia 39 0.028
601
c PRG020 Paragangliomas 3 39 0.028
602
HYP344 Hyperthyroidism, Familial Gestational 39 0.028
603
ADP007 Adie Pupil 39 0.028
604
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.028
605
c CHR682 Chronic Bilirubin Encephalopathy 39 0.028
606
ALL014 Allergic Encephalomyelitis 38 0.028
607
EPD022 Epidermolysis Bullosa Pruriginosa 38 0.028
608
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.028
609
CNT060 Central Serous Chorioretinopathy 38 0.028
610
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.028
611
CRB009 Cerebritis 37 0.028
612
GGR001 Geographic Tongue 37 0.028
613
c CNG223 Congenital Methemoglobinemia 36 0.028
614
P JVN050 Juvenile Amyotrophic Lateral Sclerosis 36 0.028
615
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 0.028
616
CRY036 Cryptogenic Cirrhosis 36 0.028
617
ASC001 Ascaridiasis 35 0.028
618
END072 Endotheliitis 35 0.028
619
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.028
620
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 34 0.028
622
RTC003 Root Caries 33 0.028
623
ALR002 Al-Raqad Syndrome 33 0.028
624
c PRS136 Prostate Cancer, Hereditary, 6 33 0.028
625
HND015 Hand Skill, Relative 33 0.028
626
c PRS130 Prostate Cancer, Hereditary, 8 32 0.028
627
c BLD140 Blood Group, I System 32 0.028
628
c CRD098 Cardiomyopathy, Familial Restrictive, 3 32 0.028
629
STR019 Steroid-Induced Glaucoma 32 0.028
630
NRN002 Neuronitis 32 0.028
631
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.028
632
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.028
633
c CHR013 Chronic Apical Periodontitis 31 0.028
634
WTS001 Watson Syndrome 30 0.028
635
BRT055 Breath-Holding Spells 30 0.028
636
MRR003 Murray Valley Encephalitis 29 0.028
637
MYC088 Mycobacterium Avium Complex Infections 29 0.028
638
PST092 Posttransplant Acute Limbic Encephalitis 29 0.028
639
NVS007 Nevus of Ota 28 0.028
640
ACD011 Acid Phosphatase Deficiency 28 0.028
641
TCH005 Tièche-Jadassohn Nevus 28 0.028
642
CTR027 Cataract-Glaucoma 27 0.028
643
HNM002 Hinman Syndrome 27 0.028
644
CYT018 Cytochrome P450 2d6 Variant 27 0.028
645
URN022 Urinary Tract Infections, Recurrent 27 0.028
646
MLR020 Malaria, Mild 27 0.028
647
MTH071 Methane Production 26 0.028
648
TXC010 Toxic Myocarditis 26 0.028
649
DVR001 Diverticulitis of Colon 25 0.028
650
NRM022 Neurometabolic Disease 25 0.028
651
c MLT009 Multiple Cranial Nerve Palsy 25 0.028
652
NTH002 Nathalie Syndrome 22 0.028
653
GLS008 Glossopharyngeal Nerve Disease 22 0.028
654
BLD165 Blood Group, Colton System 20 0.028
655
HML010 Hemolytic Anemia Due to Glutathione Reductase Deficiency 19 0.028
656
AND005 Androgen Insensitivity Syndrome, Mild 19 0.028
657
CRB089 Cerebral Beriberi 18 0.028
658
GLS013 Glossodynia 18 0.028
659
MLT155 Multiple Acyl-Coa Dehydrogenase Deficiency, Severe Neonatal Type 16 0.028
660
MLT154 Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type 15 0.028
661
c KRT039 Keratoconus 2 15 0.028
662
MYC004 Mycotic Corneal Ulcer 14 0.028
663
c PHT011 Photoparoxysmal Response 3 14 0.028
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