Search results for Docosahexaenoic acid

519 hits were found for Docosahexaenoic acid

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.428
2
FTT001 Fatty Liver Disease 61 0.349
3
P LVR013 Liver Disease 68 0.334
4
P CLR023 Colorectal Cancer 99 0.291
5
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.291
6
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.252
7
ISC004 Ischemia 58 0.246
8
P HYP750 Hypertriglyceridemia, Familial 62 0.246
9
LVR012 Liver Cirrhosis 62 0.246
10
CHL068 Cholestasis 61 0.242
11
P NRB001 Neuroblastoma 72 0.240
12
P ALZ034 Alzheimer Disease 88 0.237
13
P BRS047 Breast Cancer 97 0.236
14
LPD008 Lipid Metabolism Disorder 62 0.234
15
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.229
16
P SZR006 Seizure Disorder 56 0.228
17
VSL002 Visual Epilepsy 59 0.222
18
P GLM045 Glioma 63 0.222
19
GLL048 Glial Tumor 45 0.220
20
CYS001 Cystic Fibrosis 81 0.219
21
P CRN300 Coronary Heart Disease 1 63 0.214
22
P KDN018 Kidney Disease 72 0.211
23
ACT119 Acute Promyelocytic Leukemia 63 0.210
24
BNR002 Bone Resorption Disease 48 0.210
25
HLX001 Helix Syndrome 47 0.205
26
c HYP836 Hypercholesterolemia, Familial, 1 73 0.203
27
CYT002 Cytokine Deficiency 42 0.202
28
P HPT023 Hepatocellular Carcinoma 100 0.201
29
P BPL003 Bipolar Disorder 56 0.199
30
ATH013 Atherosclerosis Susceptibility 65 0.199
31
c MJR024 Major Affective Disorder 9 41 0.199
32
c MJR022 Major Affective Disorder 8 38 0.199
33
CLT003 Colitis 62 0.198
34
NNL006 Non-Alcoholic Steatohepatitis 54 0.196
35
LPP008 Lipoprotein Quantitative Trait Locus 62 0.194
36
HYP066 Hyperglycemia 61 0.190
37
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.190
38
DRM006 Dermatitis 61 0.190
39
48X005 48,xyyy 39 0.189
40
P INF037 Inflammatory Bowel Disease 54 0.189
41
P PRS040 Prostate Cancer 97 0.188
42
DPR016 Depression 63 0.188
43
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.187
45
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.186
46
P ENC018 Encephalopathy 61 0.185
47
SPN186 Spinal Cord Injury 60 0.184
48
HYP056 Hypoglycemia 66 0.183
49
P VSC007 Vascular Disease 63 0.182
50
OST012 Osteoarthritis 78 0.182
51
ATM095 Autoimmune Disease 62 0.181
52
BRN071 Brain Injury 49 0.179
53
MNT002 Mental Depression 58 0.179
54
GLB015 Glioblastoma Multiforme 75 0.177
55
NTR005 Nutritional Deficiency Disease 62 0.177
56
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.177
57
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.175
58
ART140 Arteries, Anomalies of 52 0.174
59
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.174
60
c PRC016 Pre-Eclampsia 63 0.173
61
TRM010 Traumatic Brain Injury 51 0.170
62
PHN003 Phenylketonuria 75 0.170
63
DFC004 Deficiency Anemia 70 0.168
64
P LKM002 Leukemia 68 0.167
65
ULC004 Ulcerative Colitis 73 0.167
66
P ADN016 Adenocarcinoma 64 0.165
67
HYP266 Hypoxia 57 0.164
68
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.163
69
P PNC035 Pancreatic Cancer 84 0.163
70
HYP060 Hyperinsulinism 54 0.163
71
P MJR001 Major Depressive Disorder 68 0.163
72
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.162
73
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.162
74
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.162
75
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.162
76
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.162
77
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.162
78
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.162
79
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.162
80
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.162
81
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.162
82
CRB004 Cerebral Artery Occlusion 45 0.162
83
P OST002 Osteoporosis 74 0.160
84
P TRN020 Turner Syndrome 67 0.160
85
P MYL006 Myeloid Leukemia 60 0.159
86
c HYP595 Hypertension, Essential 84 0.157
87
P NRP001 Neuropathy 56 0.157
88
ALC007 Alcohol Dependence 66 0.156
89
PPT005 Peptic Ulcer Disease 59 0.156
90
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.156
91
P ATS364 Autism 70 0.155
92
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.155
93
ALL026 Allergic Hypersensitivity Disease 62 0.155
94
PRX001 Peroxisomal Disease 46 0.155
95
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.155
96
P CRD246 Cardiovascular System Disease 57 0.154
97
HRW001 Hair Whorl 36 0.154
98
P OVR042 Ovarian Cancer 88 0.153
99
PRT037 Pertussis 65 0.153
100
RTN023 Retinitis 46 0.153
101
NRR001 Neuroretinitis 42 0.153
102
HMN044 Human Immunodeficiency Virus Type 1 71 0.153
103
P GST044 Gastritis 56 0.152
104
P PRD008 Periodontitis 64 0.151
105
ADR022 Adrenomyeloneuropathy 38 0.151
106
PPL052 Papillomatosis, Confluent and Reticulated 33 0.151
107
P RTN008 Retinitis Pigmentosa 79 0.151
108
P DRM053 Dermatitis, Atopic 66 0.149
109
ADR007 Adrenoleukodystrophy 75 0.149
110
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.149
111
CRH001 Crohn's Disease 74 0.148
112
MYL069 Myeloma, Multiple 85 0.148
113
P MYC007 Myocardial Infarction 70 0.147
114
c CHR684 Chronic Kidney Disease 70 0.147
115
c ATS007 Autism Spectrum Disorder 67 0.146
116
P ZLL001 Zellweger Syndrome 57 0.145
117
P HRT032 Heart Disease 75 0.145
118
c ACT027 Acute Pancreatitis 60 0.144
119
CRD132 Cardiac Conduction Defect 58 0.144
120
P CHL066 Cholangitis 51 0.144
121
P LNG032 Lung Cancer 98 0.143
122
c PCH010 Pachyonychia Congenita 3 44 0.142
123
P RTN016 Retinal Degeneration 53 0.142
124
CNG034 Congestive Heart Failure 69 0.142
125
P NTR004 Neutropenia 63 0.141
126
P BND020 Bone Disease 59 0.139
127
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.139
128
INS024 Insulin-Like Growth Factor I 79 0.139
129
P BLD134 Bladder Cancer 79 0.139
130
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.138
131
P LTR001 Lateral Sclerosis 54 0.137
132
P RTN024 Retinoblastoma 73 0.137
133
c FML008 Familial Retinoblastoma 53 0.136
134
ADN018 Adenoma 59 0.136
135
CHL079 Children's Interstitial Lung Disease 26 0.135
136
P DBT009 Diabetes Mellitus 64 0.135
137
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.134
138
HPT004 Hepatic Coma 45 0.134
139
GST033 Gestational Diabetes 61 0.134
140
HMC014 Homocysteinemia 53 0.133
141
P MCR115 Microvascular Complications of Diabetes 5 66 0.132
142
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.131
143
STR067 Stroke, Ischemic 81 0.131
144
END086 End Stage Renal Disease 51 0.130
145
c RHB024 Rhabdomyosarcoma 2 67 0.130
146
P GLM007 Glomerulonephritis 57 0.129
147
c MCR120 Microvascular Complications of Diabetes 7 47 0.129
148
c MCR113 Microvascular Complications of Diabetes 3 52 0.129
149
c LKM061 Leukemia, Acute Myeloid 84 0.129
150
PRT036 Peritonitis 64 0.129
151
c ACT071 Acute Kidney Failure 60 0.129
152
c MCR130 Microvascular Complications of Diabetes 6 41 0.129
153
c MCR133 Microvascular Complications of Diabetes 4 41 0.129
154
P CNR004 Cone-Rod Dystrophy 2 73 0.128
155
P GST053 Gastric Cancer 83 0.128
156
IRN002 Iron Metabolism Disease 57 0.126
157
OST159 Osteogenic Sarcoma 66 0.126
158
HPT019 Hepatic Encephalopathy 60 0.126
159
CRB039 Cerebrovascular Disease 67 0.125
160
47X002 47,xyy 49 0.123
161
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.123
162
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.123
163
RCK004 Rickets 68 0.123
164
LNG099 Lung Disease 60 0.122
165
P LPS004 Lupus Erythematosus 61 0.121
166
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.121
167
P ART022 Arthritis 69 0.121
168
P PRP019 Peripheral Nervous System Disease 58 0.120
169
SKN016 Skin Disease 63 0.120
170
EMB004 Embryonal Carcinoma 56 0.120
171
AGN016 Aging 56 0.119
172
P ART021 Arteriosclerosis 54 0.119
173
P BCL017 B-Cell Lymphoma 58 0.118
174
HLC007 Helicobacter Pylori Infection 59 0.118
175
ALL014 Allergic Encephalomyelitis 38 0.117
176
ENT011 Enterocolitis 51 0.117
177
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.116
178
c ACT075 Acute Myocardial Infarction 57 0.116
179
CRV035 Cervical Cancer 76 0.115
180
P ATR011 Atrial Fibrillation 66 0.115
181
c SYS001 Systemic Lupus Erythematosus 86 0.115
182
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.115
183
MDD011 Mood Disorder 62 0.115
184
DBT010 Diabetic Neuropathy 54 0.115
185
P SCL009 Sclerosing Cholangitis 48 0.115
186
P EPL164 Epilepsy 71 0.114
187
BCT022 Bacterial Infectious Disease 56 0.114
188
P SKN015 Skin Carcinoma 66 0.114
189
P HYP086 Hypothyroidism 69 0.113
190
GLC003 Glucose Intolerance 54 0.113
191
c DBT099 Diabetes Mellitus, Type I 65 0.113
192
VTM002 Vitamin B12 Deficiency 48 0.113
193
P ALC033 Alcohol Use Disorder 58 0.113
194
P PHC003 Pheochromocytoma 71 0.113
195
P MLN008 Melanoma 69 0.112
196
ADR040 Adrenal Gland Pheochromocytoma 46 0.112
197
P OVR082 Overgrowth Syndrome 50 0.112
198
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.111
199
SQM006 Squamous Cell Carcinoma 60 0.111
200
P LNG064 Lung Cancer Susceptibility 3 78 0.111
201
P PRK057 Parkinson Disease, Late-Onset 78 0.111
202
c CHL119 Cholangitis, Primary Sclerosing 57 0.111
203
P FBR017 Fibrosarcoma 56 0.110
204
HYP005 Hypokalemia 55 0.110
205
HMP009 Haemophilus Influenzae 43 0.109
206
PRN019 Perinatal Necrotizing Enterocolitis 59 0.109
207
P RHM011 Rheumatoid Arthritis 80 0.108
208
P MPL001 Maple Syrup Urine Disease 69 0.108
209
P MSC005 Muscular Dystrophy 66 0.108
210
BRN024 Bronchitis 68 0.108
211
P MSC003 Muscular Atrophy 52 0.108
212
MTH071 Methane Production 26 0.108
213
c MGR028 Migraine with or Without Aura 1 67 0.107
214
HYP081 Hypolipoproteinemia 51 0.107
215
P CTR002 Cataract 60 0.107
216
EYD002 Eye Disease 58 0.107
217
BRN004 Brain Edema 56 0.107
218
P PNC044 Pancreatitis 61 0.106
219
KRT002 Keratomalacia 47 0.106
220
P EXN002 Exanthem 57 0.105
221
PST021 Postpartum Depression 50 0.105
222
P PLM036 Pulmonary Fibrosis 65 0.105
223
CNT047 Contact Dermatitis 58 0.104
224
P SCH015 Schizophrenia 74 0.104
225
ATX019 Ataxia with Vitamin E Deficiency 42 0.104
226
ANX004 Anoxia 40 0.104
227
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.104
228
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.103
229
P HYP076 Hyperthyroidism 55 0.103
230
c INH020 Inherited Metabolic Disorder 47 0.102
231
P ALP008 Alopecia 54 0.102
232
P THR014 Thrombocytopenia 67 0.102
233
TTN003 Tetanus 65 0.102
234
P DMN002 Dementia 66 0.102
235
ANX010 Anxiety 73 0.101
236
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.101
237
P TMP001 Temporal Lobe Epilepsy 50 0.101
238
IGG001 Iga Glomerulonephritis 48 0.101
239
ACQ007 Acquired Immunodeficiency Syndrome 60 0.100
240
BRN056 Bronchopulmonary Dysplasia 57 0.099
241
P RSP003 Respiratory Failure 74 0.099
242
URL001 Urolithiasis 45 0.099
243
ATS010 Autosomal Recessive Disease 48 0.099
244
c SML038 Small Cell Cancer of the Lung 65 0.098
245
PRS045 Prostatic Hypertrophy 53 0.098
246
P AST007 Astrocytoma 51 0.098
247
c EXD008 Exudative Vitreoretinopathy 1 71 0.098
248
TXC005 Toxic Shock Syndrome 62 0.098
249
P PLM037 Pulmonary Hypertension 67 0.097
250
c FNC043 Fanconi Anemia, Complementation Group E 62 0.097
251
P LKM062 Leukemia, Acute Lymphoblastic 69 0.097
252
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.096
253
ADL002 Adult Syndrome 70 0.095
254
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.095
255
P RTN018 Retinal Disease 53 0.095
256
P TRM003 Tremor 54 0.095
257
P LYM118 Lymphoma 68 0.095
258
c ACT073 Acute Leukemia 58 0.095
259
ANG054 Angina Pectoris 66 0.094
260
c VRL010 Viral Hepatitis 52 0.093
261
SVR004 Severe Combined Immunodeficiency 73 0.093
262
P INF032 Infertility 57 0.093
263
c LKM063 Leukemia, Chronic Myeloid 72 0.093
264
MMM001 Mammary Paget's Disease 53 0.092
265
P RHN004 Rhinitis 57 0.092
266
P ECL001 Eclampsia 50 0.092
267
P HDC001 Headache 57 0.092
268
P INS002 in Situ Carcinoma 53 0.092
269
TRN015 Transient Cerebral Ischemia 63 0.092
270
P PNM007 Pneumonia 68 0.092
271
P AMY004 Amyloidosis 70 0.092
272
c ATR087 Atrial Standstill 1 75 0.091
273
P SCK005 Sickle Cell Disease 50 0.091
274
P SPP010 Suppressor of Tumorigenicity 3 51 0.091
275
AST005 Asthma 76 0.089
276
PRS021 Prostatic Adenoma 51 0.089
277
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.089
278
GNG013 Gingivitis 59 0.089
279
P DYS154 Dystonia 65 0.089
280
GST050 Gastrointestinal System Disease 56 0.088
281
PRS129 Prostatic Hyperplasia, Benign 49 0.087
282
P MLN007 Male Infertility 55 0.087
283
CHR074 Choriocarcinoma 47 0.086
284
P FML011 Familial Adenomatous Polyposis 72 0.085
285
PRP027 Peripheral Vascular Disease 71 0.085
286
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.085
287
DPH001 Diphtheria 60 0.084
288
ALL006 Allergic Asthma 56 0.084
289
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.084
290
RFS006 Refsum Disease, Classic 64 0.083
291
MST005 Mastitis 53 0.083
292
P LKM071 Leukemia, Chronic Lymphocytic 79 0.083
293
P NPH012 Nephrotic Syndrome 60 0.082
294
P THL005 Thalassemia 60 0.082
295
SCK003 Sickle Cell Anemia 74 0.082
296
P HYP098 Hypereosinophilic Syndrome 67 0.082
297
BLR008 Bilirubin Metabolic Disorder 57 0.082
298
AMN003 Amnestic Disorder 54 0.082
299
END040 Endogenous Depression 55 0.081
300
DSS008 Disease of Mental Health 58 0.081
301
P OBS001 Obstructive Jaundice 50 0.081
302
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.081
303
ALL003 Allergic Rhinitis 67 0.081
304
LYM019 Lymphosarcoma 46 0.081
305
BRN028 Brain Cancer 74 0.080
306
PRT013 Portal Hypertension 59 0.080
307
c HYP272 Hypercholesterolemia, Familial, 3 44 0.079
308
P HYP265 Hypotonia 43 0.079
309
HMS001 Hemosiderosis 54 0.079
310
MSC157 Muscular Dystrophy, Duchenne Type 72 0.078
311
BLR001 Biliary Atresia 50 0.078
313
IRN001 Iron Deficiency Anemia 59 0.077
314
P RRH023 Rare Hereditary Hemochromatosis 41 0.077
315
MST004 Mast Cell Neoplasm 42 0.077
316
EXT007 Extracutaneous Mastocytoma 38 0.077
317
CLR109 Colorectal Adenocarcinoma 51 0.077
318
c HNT004 Huntington Disease-Like 2 50 0.077
319
ARG004 Argyria 27 0.077
320
VSC002 Vascular Dementia 57 0.076
321
P MDL005 Medulloblastoma 77 0.076
322
P KDN017 Kidney Cancer 60 0.076
323
PSY004 Psychotic Disorder 67 0.075
324
FDL002 Food Allergy 51 0.075
325
LNG031 Lung Benign Neoplasm 51 0.075
326
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.074
327
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.074
328
SYN007 Synovitis 54 0.073
329
P SHR001 Short Bowel Syndrome 53 0.073
330
PLC002 Plica Syndrome 36 0.073
331
DYS073 Dysphagia 50 0.073
332
P OPN001 Open-Angle Glaucoma 49 0.072
333
P HML002 Hemolytic Anemia 63 0.072
334
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.072
335
c FML035 Familial Hyperlipidemia 55 0.072
336
P MNC007 Monocytic Leukemia 53 0.072
337
c FML021 Familial Hypercholesterolemia 66 0.071
338
PST092 Posttransplant Acute Limbic Encephalitis 29 0.071
339
RDN001 Reading Disorder 40 0.071
340
GST040 Gastric Adenocarcinoma 70 0.071
341
P FTL001 Fetal Alcohol Syndrome 57 0.071
342
HDN002 Head Injury 46 0.071
343
P RHZ001 Rhizomelic Chondrodysplasia Punctata 53 0.070
344
MSC007 Muscle Hypertrophy 64 0.070
345
P SLP006 Sleep Apnea 69 0.070
346
RTN020 Retinal Vascular Disease 46 0.070
347
PLC008 Placenta Disease 50 0.070
348
SCR011 Scrapie 39 0.070
349
c BRN108 Branchiootic Syndrome 1 62 0.069
350
P UVT001 Uveitis 57 0.069
351
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.069
352
CRT015 Carotid Artery Occlusion 45 0.069
353
P VSC018 Visceral Steatosis 33 0.069
354
LYM133 Lymphoma, Hodgkin, Classic 69 0.069
355
c FTL071 Fetal Akinesia Deformation Sequence 3 28 0.068
356
NTR046 Neutrophil Migration 50 0.068
357
BRS051 Breast Disease 58 0.068
358
P CLC063 Celiac Disease 1 66 0.068
359
P VSC011 Vasculitis 62 0.068
360
c HNT011 Huntington Disease-Like 3 38 0.067
361
BRK010 Burkitt Lymphoma 67 0.067
362
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.066
363
c LTN004 Late-Onset Retinal Degeneration 59 0.066
364
CHR100 Chronic Ulcer of Skin 55 0.066
365
MLK006 Milk Allergy 48 0.066
366
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.066
367
P MCR010 Microcephaly 59 0.065
368
P PRN023 Prion Disease 57 0.065
369
OVR094 Ovarian Epithelial Cancer 38 0.065
370
DRY001 Dry Eye Syndrome 47 0.065
371
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.065
372
c GLC092 Glaucoma, Primary Open Angle 62 0.065
373
PLC007 Placental Abruption 48 0.065
374
P LBR014 Leber Congenital Amaurosis 4 56 0.065
375
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.065
376
P SPN046 Spinal Muscular Atrophy 62 0.064
377
BRN002 Bronchiolitis 59 0.064
378
DMY004 Demyelinating Disease 52 0.064
379
ILS001 Ileus 51 0.064
380
NNT017 Neonatal Adrenoleukodystrophy 47 0.064
381
SPR126 Superior Semicircular Canal Dehiscence 40 0.063
382
c HMG029 Hemoglobin Se Disease 39 0.063
383
SKN019 Skin Melanoma 68 0.063
384
MCR013 Microphthalmia 57 0.063
385
IMP005 Impotence 52 0.063
386
MCL006 Macular Retinal Edema 55 0.063
387
c FML001 Familial Atrial Fibrillation 65 0.062
388
CRC021 Carcinosarcoma 62 0.062
389
RBS001 Rabies 58 0.062
390
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.062
391
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.062
392
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.062
393
RST023 Resting Heart Rate, Variation in 41 0.062
394
P CHN012 Chondrosarcoma 56 0.061
395
49X006 49, Xxxxy Syndrome 41 0.061
396
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.061
397
DBF001 D-Bifunctional Protein Deficiency 54 0.061
398
P MTR014 Motor Neuron Disease 65 0.061
399
c INF071 Inflammatory Bowel Disease 1 67 0.061
400
KHL003 Kohlschutter-Tonz Syndrome 65 0.060
401
P SBS003 Substance Abuse 55 0.060
402
TRD006 Tardive Dyskinesia 54 0.060
403
AMB002 Amblyopia 49 0.059
404
SPP007 Suppression Amblyopia 39 0.059
405
SDD001 Sudden Infant Death Syndrome 61 0.059
406
BRS099 Breast Ductal Carcinoma 62 0.059
407
PLC005 Placental Insufficiency 57 0.059
408
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.059
409
DCT002 Ductal Carcinoma in Situ 59 0.059
410
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.059
411
P DYS005 Dyslexia 40 0.059
412
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.059
413
P TRT010 Teratoma 52 0.058
414
c STR040 Stargardt Disease 3 32 0.058
415
CRB090 Cerebral Hypoxia 44 0.058
416
SPP011 Suppression of Tumorigenicity 12 59 0.058
417
MNT001 Mantle Cell Lymphoma 69 0.057
418
ETN001 Eating Disorder 60 0.057
419
P MTC069 Mitochondrial Disorders 56 0.057
420
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.057
421
P FLL037 Follicular Lymphoma 67 0.057
422
P OPT006 Optic Nerve Disease 60 0.056
423
PTH003 Pathologic Nystagmus 52 0.056
425
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.056
426
P STR022 Stargardt Disease 58 0.055
427
c BPL002 Bipolar I Disorder 49 0.055
428
KHN001 Kuhnt-Junius Degeneration 47 0.055
429
MLT157 Multiple System Atrophy 1 70 0.055
430
P MRC003 Mercury Poisoning 48 0.055
431
DBT006 Diabetic Macular Edema 48 0.055
432
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.055
433
P PRC031 Preeclampsia/eclampsia 1 38 0.054
434
KLD004 Keloid Disorder 40 0.054
435
OVR063 Overnutrition 44 0.053
436
MCP006 Mucoepidermoid Carcinoma 50 0.052
437
ALC009 Alcoholic Liver Cirrhosis 53 0.052
438
LRN003 Learning Disability 49 0.052
439
SNS003 Sensory Peripheral Neuropathy 54 0.052
440
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.052
441
GSG001 Gas Gangrene 53 0.051
442
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.051
443
RTN003 Retinal Ischemia 50 0.051
444
c FLL041 Follicular Lymphoma 1 49 0.051
445
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.051
446
PLC006 Placental Choriocarcinoma 36 0.051
447
MNG007 Manganese Poisoning 29 0.051
448
WLS001 Wilson Disease 71 0.050
449
c ALP101 Alpha-Thalassemia 62 0.050
450
PLL012 Pollen Allergy 46 0.050
451
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.050
452
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.049
453
c NNS043 Nonsyndromic Retinitis Pigmentosa 27 0.049
454
P CRB088 Cerebral Atrophy 37 0.049
455
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.048
456
c BRS049 Breast Carcinoma in Situ 51 0.048
457
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.048
458
CNG092 Congenital Extrahepatic Portosystemic Shunt 23 0.048
459
ASP026 Asplenia, Isolated Congenital 44 0.047
460
DVL001 Developmental Coordination Disorder 34 0.046
461
DVL005 Developmental Dyspraxia 23 0.046
462
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.046
463
PRT082 Preterm Premature Rupture of the Membranes 54 0.045
464
MCN017 Meconium Ileus 52 0.045
465
SYN036 Syncope 45 0.044
466
P PRL003 Proliferative Glomerulonephritis 44 0.044
467
GRM010 Germ Cells Tumors 34 0.044
468
BWN001 Bowen-Conradi Syndrome 52 0.044
469
c SPR086 Spermatogenic Failure 3 44 0.044
470
LBL001 Lobular Neoplasia 56 0.043
471
AYM001 Ayme-Gripp Syndrome 57 0.043
472
c ATM099 Autoimmune Uveitis 45 0.043
473
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.043
474
CYS005 Cysticercosis 53 0.043
475
PRV004 Periventricular Leukomalacia 52 0.043
476
EXS001 Exostosis 46 0.043
477
LNG091 Lung Mucoepidermoid Carcinoma 35 0.042
478
P CRB059 Cerebellar Degeneration 37 0.042
479
FND002 Fundus Dystrophy 55 0.041
480
APR001 Apraxia 52 0.041
481
c SPN284 Spinocerebellar Ataxia 38 41 0.041
482
NRX001 Neuroaxonal Dystrophy 35 0.041
483
P MLN069 Melanoma, Uveal 59 0.041
484
c INH030 Inherited Retinal Disorder 51 0.041
485
c PRG020 Paragangliomas 3 39 0.041
486
SMT004 Smith-Lemli-Opitz Syndrome 70 0.040
487
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.040
488
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.040
489
c STR084 Stargardt Disease 1 47 0.040
490
c PLN017 Peeling Skin Syndrome 1 38 0.040
491
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.039
492
CLN044 Colon Adenoma 44 0.039
493
c OPT053 Optic Atrophy 1 63 0.039
494
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.039
495
c PRX062 Peroxisome Biogenesis Disorder 8b 25 0.039
496
INT253 Intestinal Benign Neoplasm 45 0.038
497
MSC152 Muscular Dystrophy, Becker Type 63 0.036
498
c RHZ011 Rhizomelic Chondrodysplasia Punctata, Type 1 52 0.036
499
TRP014 Triploidy 42 0.036
500
ACT162 Acute Sensory Ataxic Neuropathy 26 0.036
501
END021 Endomyocardial Fibrosis 49 0.035
502
PLT031 Platelet Membrane Fluidity 29 0.035
503
SHR107 Short Stature-Obesity Syndrome 26 0.035
504
P BRG001 Brugada Syndrome 71 0.033
505
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.033
506
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.033
507
P USH001 Usher Syndrome 60 0.032
508
P NPH005 Nephronophthisis 59 0.032
509
P VTL001 Vitelliform Macular Dystrophy 42 0.032
510
DBT081 Diabetic Encephalopathy 37 0.032
511
INT358 Intestinal Polyposis Syndrome 25 0.032
512
c MCR269 Microcephaly 15, Primary, Autosomal Recessive 33 0.031
513
BRT055 Breath-Holding Spells 30 0.031
514
CHR003 Cherubism 57 0.029
515
IMM102 Immunodeficiency 14 53 0.029
516
P SPS008 Spastic Ataxia 41 0.029
517
BST007 Best Vitelliform Macular Dystrophy 34 0.029
518
PDP001 Pedophilia 30 0.029
519
PRP002 Periapical Granuloma 39 0.027
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