Search results for Glycerol

790 hits were found for Glycerol

# Family MCID Name MIFTS Score
1
GLY014 Glycerol Kinase Deficiency 49 9.773
2
GLY102 Glycerol Quantitative Trait Locus 13 5.119
3
GLY100 Glycerol Kinase 2 12 5.119
4
CHR387 Chromosome Xp21 Deletion Syndrome 35 4.706
5
GLY101 Glycerol Kinase 3 Pseudogene 7 3.964
6
BTG004 Beta-Glycerol Phosphatase 6 3.251
7
DSR071 Disorder of Glycerol Metabolism 4 2.325
8
c ACT071 Acute Kidney Failure 60 0.350
9
P KDN018 Kidney Disease 72 0.343
10
TRG002 Trigeminal Neuralgia 60 0.271
11
P MSC005 Muscular Dystrophy 66 0.186
12
MSC157 Muscular Dystrophy, Duchenne Type 72 0.169
13
MNR012 Meniere Disease 57 0.167
14
HYP056 Hypoglycemia 66 0.148
15
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.148
16
BRN004 Brain Edema 56 0.137
17
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.132
18
P MNN013 Meningitis 66 0.129
19
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.129
20
MTH071 Methane Production 26 0.121
21
c BCT007 Bacterial Meningitis 55 0.118
22
HYP066 Hyperglycemia 61 0.112
23
INT075 Intracranial Hypertension 53 0.112
24
HMP009 Haemophilus Influenzae 43 0.112
25
P HYP750 Hypertriglyceridemia, Familial 62 0.109
26
48X005 48,xyyy 39 0.109
27
OCL069 Ocular Motor Apraxia 51 0.106
28
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.100
29
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.100
30
P DRM053 Dermatitis, Atopic 66 0.100
31
HYP780 Hypoadrenocorticism, Familial 63 0.100
32
FTT001 Fatty Liver Disease 61 0.100
33
P HRD011 Hereditary Spherocytosis 60 0.100
34
P GLM045 Glioma 63 0.097
35
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.097
36
ACT003 Acute Kidney Tubular Necrosis 45 0.097
37
P MYP004 Myopathy 70 0.093
38
P SNS001 Sensorineural Hearing Loss 60 0.093
39
GLL048 Glial Tumor 45 0.093
40
c STC015 Stickler Syndrome, Type I 40 0.093
41
TXC005 Toxic Shock Syndrome 62 0.089
42
P HYP076 Hyperthyroidism 55 0.089
43
HYP060 Hyperinsulinism 54 0.089
44
ALL026 Allergic Hypersensitivity Disease 62 0.086
45
DRM006 Dermatitis 61 0.086
46
P HDC001 Headache 57 0.086
47
ADR049 Adrenal Hypoplasia, Congenital 54 0.086
48
STR067 Stroke, Ischemic 81 0.082
49
CNT047 Contact Dermatitis 58 0.082
50
TRM010 Traumatic Brain Injury 51 0.082
51
URC002 Urea Cycle Disorder 51 0.082
52
HLX001 Helix Syndrome 47 0.082
53
P NTR004 Neutropenia 63 0.077
54
P THL005 Thalassemia 60 0.077
55
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.077
56
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.077
57
FRC001 Fructose-1,6-Bisphosphatase Deficiency 49 0.077
58
BRN071 Brain Injury 49 0.077
59
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.077
60
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.077
61
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.077
62
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.077
63
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.077
64
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.077
65
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.077
66
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.077
67
MLR004 Malaria 81 0.073
68
P LVR013 Liver Disease 68 0.073
69
KRT019 Keratitis, Hereditary 65 0.073
70
SKN016 Skin Disease 63 0.073
71
VSL002 Visual Epilepsy 59 0.073
72
IRN002 Iron Metabolism Disease 57 0.073
73
P SZR006 Seizure Disorder 56 0.073
74
MTB004 Metabolic Acidosis 50 0.073
75
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.073
76
BRN024 Bronchitis 68 0.068
77
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.068
78
CHL068 Cholestasis 61 0.068
79
P ENC018 Encephalopathy 61 0.068
80
HDN002 Head Injury 46 0.068
81
P HPT023 Hepatocellular Carcinoma 100 0.063
82
c HYP836 Hypercholesterolemia, Familial, 1 73 0.063
83
DFC004 Deficiency Anemia 70 0.063
84
P HYP086 Hypothyroidism 69 0.063
85
P DBT009 Diabetes Mellitus 64 0.063
86
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.063
87
c BRN108 Branchiootic Syndrome 1 62 0.063
88
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.063
89
P CTR002 Cataract 60 0.063
90
SLP001 Sleeping Sickness 54 0.063
91
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.063
92
c MLG068 Malignant Glioma 46 0.063
93
P CLR023 Colorectal Cancer 99 0.058
94
GLB015 Glioblastoma Multiforme 75 0.058
95
ADR007 Adrenoleukodystrophy 75 0.058
96
P ASP006 Aspergillosis 69 0.058
97
P TRN020 Turner Syndrome 67 0.058
98
P HYD006 Hydrocephalus 66 0.058
99
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.058
100
MSC152 Muscular Dystrophy, Becker Type 63 0.058
101
LPD008 Lipid Metabolism Disorder 62 0.058
102
P TRC086 Trichohepatoenteric Syndrome 1 62 0.058
103
HPT019 Hepatic Encephalopathy 60 0.058
104
INS001 Insulinoma 60 0.058
105
P GLY013 Glycogen Storage Disease 60 0.058
106
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.058
107
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.058
108
c ACT134 Acute Liver Failure 56 0.058
109
AGN016 Aging 56 0.058
110
NTR046 Neutrophil Migration 50 0.058
111
IRR003 Irritant Dermatitis 49 0.058
112
c INH020 Inherited Metabolic Disorder 47 0.058
113
NSS002 Neisseria Meningitidis Infection 47 0.058
114
MNN020 Meningococcal Infection 46 0.058
115
HPT004 Hepatic Coma 45 0.058
116
CRB004 Cerebral Artery Occlusion 45 0.058
117
P BCT020 Bacteremia 2 44 0.058
118
CYT002 Cytokine Deficiency 42 0.058
119
ANX004 Anoxia 40 0.058
120
ADR022 Adrenomyeloneuropathy 38 0.058
121
HRW001 Hair Whorl 36 0.058
122
c BTT014 Beta-Thalassemia 74 0.052
123
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.052
124
P NRB001 Neuroblastoma 72 0.052
125
P MYC007 Myocardial Infarction 70 0.052
126
ANG054 Angina Pectoris 66 0.052
127
TTN003 Tetanus 65 0.052
128
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.052
129
LSH001 Leishmaniasis 63 0.052
130
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.052
131
GST033 Gestational Diabetes 61 0.052
132
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.052
133
EYD002 Eye Disease 58 0.052
134
ALL010 Allergic Contact Dermatitis 56 0.052
135
MCL006 Macular Retinal Edema 55 0.052
136
P HYP730 Hypogonadotropic Hypogonadism 52 0.052
137
PTH003 Pathologic Nystagmus 52 0.052
138
HMG002 Hemoglobinuria 50 0.052
139
HYP080 Hypogonadism 50 0.052
140
47X002 47,xyy 49 0.052
141
CRT015 Carotid Artery Occlusion 45 0.052
142
SPS057 Spasticity 45 0.052
143
ATX019 Ataxia with Vitamin E Deficiency 42 0.052
144
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.052
145
P KLZ004 Kala-Azar 1 41 0.052
146
c PRG106 Progressive Muscular Dystrophy 33 0.052
147
c HYP595 Hypertension, Essential 84 0.045
148
P GST053 Gastric Cancer 83 0.045
149
CYS001 Cystic Fibrosis 81 0.045
150
AST005 Asthma 76 0.045
151
LPT014 Leptin Deficiency or Dysfunction 74 0.045
152
c MNN043 Meningioma, Familial 74 0.045
153
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.045
154
DWN001 Down Syndrome 70 0.045
155
P HPT021 Hepatitis 67 0.045
156
CRB039 Cerebrovascular Disease 67 0.045
157
c RHB024 Rhabdomyosarcoma 2 67 0.045
158
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.045
159
SRC014 Sarcoma 65 0.045
160
IRR002 Irritable Bowel Syndrome 65 0.045
161
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.045
162
MNN042 Meningioma, Radiation-Induced 62 0.045
163
LVR012 Liver Cirrhosis 62 0.045
164
NTR005 Nutritional Deficiency Disease 62 0.045
165
LNG099 Lung Disease 60 0.045
166
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.045
167
CHL014 Cholera 59 0.045
168
CHL123 Chlamydia 59 0.045
169
IRN001 Iron Deficiency Anemia 59 0.045
170
P ZLL001 Zellweger Syndrome 57 0.045
171
P RHN004 Rhinitis 57 0.045
172
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.045
173
BLR008 Bilirubin Metabolic Disorder 57 0.045
174
c GRV008 Graves Disease 1 56 0.045
175
HYP005 Hypokalemia 55 0.045
176
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.045
177
VSC003 Visceral Leishmaniasis 55 0.045
178
THR013 Thoracic Outlet Syndrome 54 0.045
179
SPN035 Spindle Cell Sarcoma 53 0.045
180
P INT068 Intestinal Disease 53 0.045
181
PNG002 Pain Agnosia 51 0.045
182
RYS001 Reye Syndrome 51 0.045
183
ILS001 Ileus 51 0.045
184
SPN021 Spinal Meningioma 50 0.045
185
AZS001 Azoospermia 50 0.045
186
TRY001 Trypanosomiasis 50 0.045
187
c DRM054 Dermatitis, Atopic, 2 44 0.045
188
DYS032 Dystrophinopathies 43 0.045
189
PNM013 Pneumococcal Meningitis 42 0.045
190
P CLS010 Cluster Headache 42 0.045
191
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.045
192
KLB003 Klebsiella Pneumonia 41 0.045
193
SCR001 Secretory Meningioma 41 0.045
194
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.045
195
GLC008 Glucose Metabolism Disease 40 0.045
196
CRB086 Cerebral Aneurysms 40 0.045
197
P OTT001 Otitis Externa 39 0.045
198
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.045
199
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.045
200
GLS004 Glossopharyngeal Neuralgia 34 0.045
201
PPL052 Papillomatosis, Confluent and Reticulated 33 0.045
202
CND006 Candida Glabrata 32 0.045
203
OCC001 Occupational Dermatitis 29 0.045
204
PRS120 Persistent Idiopathic Facial Pain 28 0.045
205
P CYT020 Cytomegalic Congenital Adrenal Hypoplasia 23 0.045
206
P PNC035 Pancreatic Cancer 84 0.036
207
c FNC027 Fanconi Anemia, Complementation Group a 81 0.036
208
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.036
209
P RHM011 Rheumatoid Arthritis 80 0.036
210
c NRF023 Neurofibromatosis, Type Ii 80 0.036
211
INS024 Insulin-Like Growth Factor I 79 0.036
212
P PRK057 Parkinson Disease, Late-Onset 78 0.036
213
P HRT032 Heart Disease 75 0.036
214
P RSP003 Respiratory Failure 74 0.036
215
BRN028 Brain Cancer 74 0.036
216
c SPN225 Spondyloarthropathy 1 73 0.036
217
c THR092 Thrombophilia Due to Thrombin Defect 73 0.036
218
ANX010 Anxiety 73 0.036
219
P MLT020 Multiple Sclerosis 72 0.036
220
P HNT016 Huntington Disease 72 0.036
221
HMN044 Human Immunodeficiency Virus Type 1 71 0.036
222
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.036
223
ADL002 Adult Syndrome 70 0.036
224
CNG034 Congestive Heart Failure 69 0.036
225
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.036
226
CRB037 Cerebral Palsy 69 0.036
227
P LPR021 Leprosy 3 69 0.036
228
EWN003 Ewing Sarcoma 69 0.036
229
P MYC084 Mycobacterium Tuberculosis 1 68 0.036
230
c HYP768 Hyperlipoproteinemia, Type I 67 0.036
231
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.036
232
ALL003 Allergic Rhinitis 67 0.036
233
PSY004 Psychotic Disorder 67 0.036
234
c ATS007 Autism Spectrum Disorder 67 0.036
235
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.036
236
P MCR115 Microvascular Complications of Diabetes 5 66 0.036
237
PRT037 Pertussis 65 0.036
238
ATH013 Atherosclerosis Susceptibility 65 0.036
239
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.036
240
PRT036 Peritonitis 64 0.036
241
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.036
242
PLM031 Poliomyelitis 64 0.036
243
LYM017 Lyme Disease 64 0.036
244
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.036
245
P VSC007 Vascular Disease 63 0.036
246
P CRN300 Coronary Heart Disease 1 63 0.036
247
c GLY060 Glycogen Storage Disease Ia 63 0.036
248
TRN015 Transient Cerebral Ischemia 63 0.036
249
DPR016 Depression 63 0.036
250
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.036
251
ATM095 Autoimmune Disease 62 0.036
252
MDD011 Mood Disorder 62 0.036
253
c PNS012 Paine Syndrome 61 0.036
254
P ACH003 Achromatopsia 61 0.036
255
P PNC044 Pancreatitis 61 0.036
256
RTN017 Retinal Detachment 61 0.036
257
ORL011 Oral Cancer 60 0.036
258
c HRD002 Hereditary Angioedema 60 0.036
259
THY029 Thyroid Carcinoma 59 0.036
260
IGR001 Ige Responsiveness, Atopic 59 0.036
261
ADN018 Adenoma 59 0.036
262
GST045 Gastroenteritis 59 0.036
263
P ANP001 Anaplastic Large Cell Lymphoma 58 0.036
264
ANT024 Anthrax Disease 58 0.036
265
ISC004 Ischemia 58 0.036
266
P ALC033 Alcohol Use Disorder 58 0.036
267
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.036
268
NWB001 Newborn Respiratory Distress Syndrome 58 0.036
269
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.036
270
P INF032 Infertility 57 0.036
271
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 57 0.036
272
P EXN002 Exanthem 57 0.036
273
APH001 Aphthous Stomatitis 57 0.036
274
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.036
275
CMM005 Common Cold 57 0.036
276
P CRD246 Cardiovascular System Disease 57 0.036
277
HMR039 Hemorrhage, Intracerebral 57 0.036
278
HYP266 Hypoxia 57 0.036
279
P ANG015 Angioedema 57 0.036
280
BCT022 Bacterial Infectious Disease 56 0.036
281
SFT003 Soft Tissue Sarcoma 56 0.036
282
MCS002 Mucositis 56 0.036
283
P MLN007 Male Infertility 55 0.036
284
P DRR001 Diarrhea 55 0.036
285
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 55 0.036
286
P ALP106 Alport Syndrome 1, X-Linked 55 0.036
287
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.036
288
P ICH004 Ichthyosis 54 0.036
289
PLM010 Pulmonary Edema 54 0.036
290
P ART021 Arteriosclerosis 54 0.036
291
KRT006 Keratoconjunctivitis 53 0.036
292
BCT002 Bacterial Vaginosis 53 0.036
293
OCL006 Ocular Hypertension 53 0.036
294
MST005 Mastitis 53 0.036
295
GTR002 Goiter 53 0.036
296
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 53 0.036
297
NRT004 Neuritis 52 0.036
298
P RCT021 Rectum Cancer 52 0.036
299
KRT009 Keratosis 51 0.036
300
P LCT001 Lactic Acidosis 51 0.036
301
NRM004 Neuroma 51 0.036
302
HYP081 Hypolipoproteinemia 51 0.036
303
SCB001 Scabies 50 0.036
304
HPT014 Hepatorenal Syndrome 50 0.036
305
P PRS049 Persistent Mullerian Duct Syndrome 50 0.036
306
FSC004 Fasciitis 50 0.036
307
STM007 Stomatitis 50 0.036
308
ALN001 Aland Island Eye Disease 50 0.036
309
c INF145 Infantile Liver Failure Syndrome 1 50 0.036
310
c ACH020 Achromatopsia 2 50 0.036
311
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.036
312
P OCL001 Ocular Albinism 50 0.036
313
PPL021 Papilledema 49 0.036
314
KRT001 Keratoconjunctivitis Sicca 49 0.036
315
TRT020 Tritanopia 49 0.036
316
URM002 Uremia 49 0.036
317
c INV001 Invasive Aspergillosis 49 0.036
318
ATS010 Autosomal Recessive Disease 48 0.036
319
P NGH001 Night Blindness 48 0.036
320
P CLR019 Color Blindness 48 0.036
321
DBT006 Diabetic Macular Edema 48 0.036
322
RNL077 Renal Fibrosis 47 0.036
323
c PRM093 Premature Ovarian Failure 7 47 0.036
324
ALB002 Albinism 46 0.036
325
SYN036 Syncope 45 0.036
326
INT253 Intestinal Benign Neoplasm 45 0.036
327
PRL008 Paralytic Ileus 45 0.036
328
c SPR086 Spermatogenic Failure 3 44 0.036
329
P MYG005 Myoglobinuria 44 0.036
330
CRB090 Cerebral Hypoxia 44 0.036
331
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.036
332
ORL015 Oral Squamous Cell Carcinoma 43 0.036
333
P HYP265 Hypotonia 43 0.036
334
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 42 0.036
335
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.036
336
CRB025 Carbohydrate Metabolic Disorder 41 0.036
337
CLR033 Color Vision Deficiency 41 0.036
338
PRS063 Paresthesia 41 0.036
339
P MLG074 Malignant Mesenchymoma 40 0.036
340
WLL004 Wallerian Degeneration 39 0.036
341
c ACH038 Achromatopsia 7 39 0.036
342
c CHR682 Chronic Bilirubin Encephalopathy 39 0.036
343
P FML355 Familial Intrahepatic Cholestasis 38 0.036
344
MDD003 Middle Cerebral Artery Infarction 36 0.036
345
P DNT007 Dentin Sensitivity 36 0.036
346
FST010 Fasting Hypoglycemia 35 0.036
347
HNS001 Hansen's Disease 34 0.036
348
MSC012 Muscular Dystrophy, Duchenne and Becker Type 34 0.036
349
VST001 Vestibular Neuronitis 34 0.036
350
EXT065 Extraosseous Ewing Sarcoma 33 0.036
351
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.036
352
EXT052 Extraskeletal Ewing Sarcoma 33 0.036
353
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.036
354
PLY150 Polykaryocytosis Inducer 31 0.036
355
FCL007 Facial Neuralgia 27 0.036
356
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.036
357
CRN309 Cranial Neuralgia 22 0.036
358
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 0.036
359
c GLC114 Glaucoma, Primary Closed-Angle 18 0.036
361
GLC108 Gluconeogenesis Disorder 7 0.036
362
P LNG032 Lung Cancer 98 0.026
363
P BRS047 Breast Cancer 97 0.026
364
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.026
365
P ALZ034 Alzheimer Disease 88 0.026
366
P ATX030 Ataxia-Telangiectasia 82 0.026
367
P GLM040 Glioma Susceptibility 1 81 0.026
368
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.026
369
P BLD134 Bladder Cancer 79 0.026
370
P RTN008 Retinitis Pigmentosa 79 0.026
371
P LNG064 Lung Cancer Susceptibility 3 78 0.026
372
P MDL005 Medulloblastoma 77 0.026
373
SCK003 Sickle Cell Anemia 74 0.026
374
P SCH015 Schizophrenia 74 0.026
375
CRH001 Crohn's Disease 74 0.026
376
SVR004 Severe Combined Immunodeficiency 73 0.026
377
ULC004 Ulcerative Colitis 73 0.026
378
P CNR004 Cone-Rod Dystrophy 2 73 0.026
379
P RTN024 Retinoblastoma 73 0.026
380
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.026
381
P GRF003 Graft-Versus-Host Disease 72 0.026
382
OTT002 Otitis Media 72 0.026
383
c EXD008 Exudative Vitreoretinopathy 1 71 0.026
384
WLS001 Wilson Disease 71 0.026
385
PRP027 Peripheral Vascular Disease 71 0.026
386
P EPL164 Epilepsy 71 0.026
387
P ATS364 Autism 70 0.026
388
MYL009 Myelodysplastic Syndrome 70 0.026
389
c CHR684 Chronic Kidney Disease 70 0.026
390
c PNC108 Pancreatitis, Hereditary 70 0.026
391
PLM001 Pulmonary Tuberculosis 69 0.026
392
P ART022 Arthritis 69 0.026
393
ART016 Aortic Aneurysm 69 0.026
394
P ANG001 Angelman Syndrome 69 0.026
395
P LYM118 Lymphoma 68 0.026
396
P CRN037 Craniosynostosis 68 0.026
397
P LKM002 Leukemia 68 0.026
398
RCK004 Rickets 68 0.026
399
P MJR001 Major Depressive Disorder 68 0.026
400
PNC129 Pancreatic Adenocarcinoma 68 0.026
401
P THR014 Thrombocytopenia 67 0.026
402
P CRD119 Cardiac Arrest 67 0.026
403
c INF071 Inflammatory Bowel Disease 1 67 0.026
404
BRK010 Burkitt Lymphoma 67 0.026
405
P CHR012 Chronic Granulomatous Disease 67 0.026
406
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.026
407
ALC007 Alcohol Dependence 66 0.026
408
OST159 Osteogenic Sarcoma 66 0.026
409
P DMN002 Dementia 66 0.026
410
c FML021 Familial Hypercholesterolemia 66 0.026
411
P SKN015 Skin Carcinoma 66 0.026
412
P NSP012 Nasopharyngeal Carcinoma 66 0.026
413
ART001 Arterial Tortuosity Syndrome 66 0.026
414
AND002 Androgen Insensitivity Syndrome 66 0.026
415
KHL003 Kohlschutter-Tonz Syndrome 65 0.026
416
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.026
417
P ART005 Arteriovenous Malformation 65 0.026
418
P DYS154 Dystonia 65 0.026
419
PPL049 Papillon-Lefevre Syndrome 65 0.026
420
BRR014 Barrett Esophagus 65 0.026
421
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.026
422
P HRP006 Herpes Simplex 65 0.026
423
P PRS038 Personality Disorder 65 0.026
424
c DBT099 Diabetes Mellitus, Type I 65 0.026
425
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 0.026
426
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.026
427
P THY023 Thymoma 65 0.026
428
ANG020 Angiosarcoma 64 0.026
429
CLF027 Cleft Palate, Isolated 64 0.026
430
TBC004 Tobacco Addiction 64 0.026
431
CTR172 Citrullinemia, Classic 64 0.026
432
GT001 Gout 64 0.026
433
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.026
434
PRP083 Porphyria, Acute Intermittent 64 0.026
435
P PRD008 Periodontitis 64 0.026
436
RFS006 Refsum Disease, Classic 64 0.026
437
P GCH001 Gaucher's Disease 63 0.026
438
P ANR048 Aniridia 1 63 0.026
439
TYP007 Typhoid Fever 63 0.026
440
PLG002 Plague 63 0.026
441
c MLG084 Malignant Fibrous Histiocytoma 63 0.026
442
P SHR029 Short Syndrome 63 0.026
443
ANR007 Anorexia Nervosa 63 0.026
444
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.026
445
P END044 Endometriosis 63 0.026
446
c GLC092 Glaucoma, Primary Open Angle 62 0.026
447
c ALP101 Alpha-Thalassemia 62 0.026
448
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.026
449
CLT003 Colitis 62 0.026
450
c FNC043 Fanconi Anemia, Complementation Group E 62 0.026
451
P PLY014 Polycystic Kidney Disease 62 0.026
452
P PSR002 Psoriasis 62 0.026
453
c SVR001 Severe Acute Respiratory Syndrome 62 0.026
454
LPP008 Lipoprotein Quantitative Trait Locus 62 0.026
455
P VSC011 Vasculitis 62 0.026
456
PHL006 Phelan-Mcdermid Syndrome 62 0.026
457
P ACR001 Aicardi-Goutieres Syndrome 62 0.026
458
P PRP029 Porphyria 62 0.026
459
PSR001 Psoriatic Arthritis 61 0.026
460
YLL002 Yellow Fever 61 0.026
461
P ENC004 Encephalitis 61 0.026
462
CHR066 Chronic Fatigue Syndrome 61 0.026
463
RCT015 Reactive Arthritis 61 0.026
464
P SJG008 Sjogren Syndrome 61 0.026
465
ARG002 Argininosuccinic Aciduria 61 0.026
466
VRL011 Viral Infectious Disease 61 0.026
467
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.026
468
P TXP001 Toxoplasmosis 60 0.026
469
INT066 Interstitial Lung Disease 60 0.026
470
c ACT027 Acute Pancreatitis 60 0.026
471
ACN002 Acanthosis Nigricans 60 0.026
472
P ALP009 Alopecia Areata 60 0.026
473
VRC005 Varicose Veins 60 0.026
474
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.026
475
P AXN002 Axenfeld-Rieger Syndrome 59 0.026
476
PRT013 Portal Hypertension 59 0.026
477
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.026
478
P BND020 Bone Disease 59 0.026
479
c HPT016 Hepatitis B 59 0.026
480
SPN027 Spinal Stenosis 59 0.026
481
PLM033 Pulmonary Embolism 59 0.026
482
PRN019 Perinatal Necrotizing Enterocolitis 59 0.026
483
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.026
484
P BRS044 Breast Adenocarcinoma 59 0.026
485
GNG013 Gingivitis 59 0.026
486
ANR040 Aneurysm 59 0.026
487
ALP097 Alopecia Universalis Congenita 59 0.026
488
c ACT073 Acute Leukemia 58 0.026
489
P SYP003 Syphilis 58 0.026
490
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.026
491
SPR004 Supravalvular Aortic Stenosis 58 0.026
492
FBR047 Fibromyalgia 58 0.026
493
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.026
494
P MMP001 Mumps 58 0.026
495
MNT002 Mental Depression 58 0.026
496
P BNC003 Bone Cancer 58 0.026
497
CNS004 Constipation 58 0.026
498
c DWL002 Dowling-Degos Disease 1 58 0.026
499
P GLL020 Gallbladder Disease 57 0.026
500
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.026
501
P PLV020 Pelvic Organ Prolapse 57 0.026
502
BLM002 Bulimia Nervosa 57 0.026
503
c VSC019 Vesicoureteral Reflux 1 57 0.026
504
P MYM013 Moyamoya Disease 1 57 0.026
505
DSS009 Disseminated Intravascular Coagulation 57 0.026
506
c ACT075 Acute Myocardial Infarction 57 0.026
507
P PRN023 Prion Disease 57 0.026
508
THR024 Thrombosis 57 0.026
509
P PRV006 Pervasive Developmental Disorder 57 0.026
510
P FTL001 Fetal Alcohol Syndrome 57 0.026
511
INT303 Intracranial Hypertension, Idiopathic 57 0.026
512
FRC011 Fructose Intolerance, Hereditary 57 0.026
513
P BPL003 Bipolar Disorder 56 0.026
514
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.026
515
P FBR017 Fibrosarcoma 56 0.026
516
P PLY011 Polycystic Ovary Syndrome 56 0.026
517
ALL006 Allergic Asthma 56 0.026
518
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.026
519
P NRP001 Neuropathy 56 0.026
520
HMG005 Hemoglobinopathy 56 0.026
521
GST050 Gastrointestinal System Disease 56 0.026
522
SML019 Smallpox 56 0.026
523
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.026
524
GDP001 Goodpasture Syndrome 55 0.026
525
FLR001 Filarial Elephantiasis 55 0.026
526
ATR057 Atrioventricular Block 55 0.026
527
ICH001 Ichthyosis Vulgaris 55 0.026
528
NRG002 Neurogenic Bladder 55 0.026
529
P PLM034 Pulmonary Emphysema 55 0.026
530
P SBS003 Substance Abuse 55 0.026
531
c MYP132 Myopathy, Congenital 55 0.026
532
P DBT005 Diabetes Insipidus 55 0.026
533
P FNG006 Feingold Syndrome 1 55 0.026
534
END040 Endogenous Depression 55 0.026
535
HMP005 Hemiplegia 55 0.026
536
P SLM003 Salmonellosis 55 0.026
537
CLF004 Cleft Lip/palate 54 0.026
538
P NRM002 Normal Pressure Hydrocephalus 54 0.026
539
P ALP008 Alopecia 54 0.026
540
GST037 Gastroparesis 54 0.026
541
P INF037 Inflammatory Bowel Disease 54 0.026
542
ANL018 Analbuminemia 54 0.026
543
P CNG010 Congenital Stationary Night Blindness 54 0.026
544
MYM001 Myoma 54 0.026
545
NNL006 Non-Alcoholic Steatohepatitis 54 0.026
546
GST009 Gastroschisis 53 0.026
547
P END047 Endophthalmitis 53 0.026
548
RHM028 Rheumatic Heart Disease 53 0.026
549
P RHZ001 Rhizomelic Chondrodysplasia Punctata 53 0.026
550
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 0.026
551
CRH005 Crohn's Colitis 53 0.026
552
P RTN016 Retinal Degeneration 53 0.026
553
NVS001 Neovascular Glaucoma 53 0.026
554
P ALT001 Alternating Hemiplegia of Childhood 53 0.026
555
CLF001 Cleft Lip 53 0.026
556
NNT012 Neonatal Jaundice 53 0.026
557
NRT001 Neurotic Disorder 53 0.026
558
c FML008 Familial Retinoblastoma 53 0.026
559
c PSR017 Psoriasis 2 53 0.026
560
P RTN018 Retinal Disease 53 0.026
561
c CNT035 Central Nervous System Disease 52 0.026
562
EXP004 Exophthalmos 52 0.026
563
c VRL010 Viral Hepatitis 52 0.026
564
PST011 Pustulosis of Palm and Sole 52 0.026
565
IMP005 Impotence 52 0.026
566
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.026
567
ART140 Arteries, Anomalies of 52 0.026
568
c THY107 Thymoma, Familial 52 0.026
569
P THY032 Thyroiditis 52 0.026
570
c PSR023 Psoriasis 1 52 0.026
571
c RHZ011 Rhizomelic Chondrodysplasia Punctata, Type 1 52 0.026
572
LGN006 Legionnaire Disease 52 0.026
573
ART074 Aortic Dissection 52 0.026
574
P TRT010 Teratoma 52 0.026
575
SPS003 Spastic Diplegia 51 0.026
576
THR004 Thrombocytosis 51 0.026
577
P SPP010 Suppressor of Tumorigenicity 3 51 0.026
578
FDL002 Food Allergy 51 0.026
579
MLT134 Multiple Pterygium Syndrome, Lethal Type 51 0.026
580
ENT011 Enterocolitis 51 0.026
581
CCC002 Coccidiosis 51 0.026
582
BLL003 Bell's Palsy 51 0.026
583
TNG007 Tongue Carcinoma 51 0.026
584
ASP003 Aseptic Meningitis 51 0.026
585
P AST007 Astrocytoma 51 0.026
586
END086 End Stage Renal Disease 51 0.026
587
HYP781 Hypoascorbemia 51 0.026
588
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.026
589
P OVR082 Overgrowth Syndrome 50 0.026
590
P 46X052 46,xx Sex Reversal 1 50 0.026
591
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.026
592
BRN009 Burning Mouth Syndrome 50 0.026
593
CHL122 Cholesteatoma of Middle Ear 50 0.026
594
PLC008 Placenta Disease 50 0.026
595
HYP748 Hypertelorism 50 0.026
596
DYS073 Dysphagia 50 0.026
597
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.026
598
VGN020 Vaginal Disease 49 0.026
599
CRP032 Corpus Callosum, Agenesis of 49 0.026
600
CCN002 Cocaine Abuse 49 0.026
601
XNT003 Xanthomatosis 49 0.026
602
P OPN001 Open-Angle Glaucoma 49 0.026
603
SLD003 Sialadenitis 49 0.026
604
BKR002 Baker-Gordon Syndrome 49 0.026
605
MNN009 Meningoencephalitis 49 0.026
606
P CTN015 Cutaneous T Cell Lymphoma 49 0.026
607
VCC001 Vaccinia 49 0.026
608
LRN003 Learning Disability 49 0.026
609
BNR002 Bone Resorption Disease 48 0.026
610
P HYP058 Hypervitaminosis a 48 0.026
611
NCR007 Necrotizing Fasciitis 48 0.026
612
ASP007 Aspiration Pneumonia 48 0.026
613
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.026
614
VTM033 Vitamin K Deficiency Bleeding 48 0.026
615
CLS016 Clostridium Difficile Colitis 48 0.026
616
SPL018 Splenomegaly 48 0.026
617
BBS001 Babesiosis 48 0.026
618
MDD010 Middle Ear Disease 48 0.026
619
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.026
620
NNT017 Neonatal Adrenoleukodystrophy 47 0.026
621
DRY001 Dry Eye Syndrome 47 0.026
622
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.026
623
P CRN028 Corneal Ulcer 47 0.026
624
SPH010 Sphingolipidosis 47 0.026
625
P INN002 Inner Ear Disease 47 0.026
626
c PSR032 Psoriasis 11 47 0.026
627
KRT002 Keratomalacia 47 0.026
628
P KRN004 Kernicterus 47 0.026
629
CRD137 Cardiogenic Shock 47 0.026
630
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.026
631
MCL009 Mcleod Syndrome 46 0.026
632
RTN023 Retinitis 46 0.026
633
ATN005 Autonomic Dysfunction 46 0.026
634
KRT013 Keratolytic Winter Erythema 46 0.026
635
P HMR005 Hemorrhoid 46 0.026
636
VGN019 Vaginal Discharge 46 0.026
637
c DRR009 Diarrhea 6 46 0.026
638
ANR004 Anuria 46 0.026
639
PRX001 Peroxisomal Disease 46 0.026
640
URT010 Ureteral Obstruction 45 0.026
641
NWC001 Newcastle Disease 45 0.026
642
P CMM008 Communicating Hydrocephalus 45 0.026
643
LYD001 Leydig Cell Tumor 45 0.026
644
GRD001 Giardiasis 45 0.026
645
CNT017 Central Nervous System Origin Vertigo 45 0.026
646
PNT038 Peanut Allergy 45 0.026
647
CRT039 Corticosterone Methyloxidase Type I Deficiency 45 0.026
648
ANS012 Anus Disease 45 0.026
649
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.026
650
P CHR345 Chronic Pain 44 0.026
651
SBC016 Subacute Delirium 44 0.026
652
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.026
653
ORG002 Organic Acidemia 44 0.026
654
P SDR002 Siderosis 44 0.026
655
KWS001 Kwashiorkor 44 0.026
656
c SPH013 Spherocytosis, Type 1 44 0.026
657
INT258 Interstitial Nephritis, Karyomegalic 44 0.026
658
c PRM038 Primary Agammaglobulinemia 44 0.026
659
HPT082 Hepatic Adenomas, Familial 44 0.026
660
c NGH010 Night Blindness, Congenital Stationary, Autosomal Dominant 2 44 0.026
661
CVD001 Covid-19 44 0.026
662
RFR003 Refractive Error 43 0.026
663
c HYP575 Hypotrichosis 7 43 0.026
664
P CRN026 Corneal Edema 43 0.026
665
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.026
666
PLY068 Polysubstance Abuse 43 0.026
667
MDD018 Middle East Respiratory Syndrome 43 0.026
668
P MJR007 Major Affective Disorder 1 43 0.026
669
VRL003 Variola Major 42 0.026
670
HYP457 Hypertrophic Scars 42 0.026
671
URM005 Uremic Pruritus 42 0.026
672
PHY002 Physical Disorder 42 0.026
673
c PSR028 Psoriasis 7 42 0.026
674
P LBY004 Labyrinthitis 42 0.026
675
EST005 Esotropia 42 0.026
676
BCK006 Back Pain 42 0.026
677
P HYP087 Hypotrichosis 42 0.026
678
MYF002 Myofascial Pain Syndrome 42 0.026
679
NRR001 Neuroretinitis 42 0.026
680
ARC002 Arachnoiditis 42 0.026
681
PDC001 Podoconiosis 41 0.026
682
ELP001 Elephantiasis 41 0.026
683
MTL005 Metal Allergy 41 0.026
684
c PSR018 Psoriasis 13 41 0.026
685
c MJR024 Major Affective Disorder 9 41 0.026
686
P CRB045 Cerebellar Hypoplasia 41 0.026
687
RDN001 Reading Disorder 40 0.026
688
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.026
689
FNG016 Fungal Keratitis 40 0.026
690
ANG049 Angioedema Induced by Ace Inhibitors 40 0.026
691
c GLY016 Glycogen Storage Disease Ib 40 0.026
692
c SPH014 Spherocytosis, Type 2 40 0.026
693
OCL010 Ocular Hypotension 39 0.026
694
HNZ004 Heinz Body Anemias 39 0.026
695
HYP141 Hyperphenylalaninemia 39 0.026
696
ADP007 Adie Pupil 39 0.026
697
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.026
698
ALL014 Allergic Encephalomyelitis 38 0.026
699
c PLY105 Polycystic Ovary Syndrome 1 38 0.026
700
HYP264 Hypertonia 38 0.026
701
c ATM075 Autoimmune Encephalitis 38 0.026
702
c DFN352 Deafness, Autosomal Recessive 8 38 0.026
703
HYP835 Hypothalamic Obesity 38 0.026
704
VSM001 Vasomotor Rhinitis 38 0.026
705
c HNT011 Huntington Disease-Like 3 38 0.026
706
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.026
707
c MJR022 Major Affective Disorder 8 38 0.026
708
SWL001 Swallowing Disorders 38 0.026
709
CRT004 Carotid Artery Thrombosis 38 0.026
710
P HMF004 Hemifacial Spasm 38 0.026
711
46X012 46,xy Partial Gonadal Dysgenesis 37 0.026
712
ATM052 Autoimmune Disease 1 37 0.026
713
CNJ007 Conjunctivochalasis 37 0.026
714
c STC013 Stickler Syndrome, Type Ii 36 0.026
715
PYL017 Pyle Disease 36 0.026
716
BRN018 Borna Disease 36 0.026
717
ABD010 Abdominal Wall Defect 36 0.026
718
SPN354 Spinal Arachnoiditis 36 0.026
720
c PRV019 Periventricular Nodular Heterotopia 1 36 0.026
721
P MTP001 Metaphyseal Dysplasia 36 0.026
722
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.026
723
INT003 Intracranial Hypotension 35 0.026
724
PRM329 Premature Aging 35 0.026
725
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.026
726
c MJR008 Major Affective Disorder 2 35 0.026
727
ATX010 Ataxia Neuropathy Spectrum 34 0.026
728
BWN003 Bowenoid Papulosis 34 0.026
729
c 46X081 46,xx Sex Reversal 34 0.026
730
HMN016 Hemangioendothelioma 34 0.026
731
c MYM004 Moyamoya Disease 2 34 0.026
732
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 34 0.026
733
NNT011 Neonatal Anemia 34 0.026
734
c HYP547 Hypogonadotropic Hypogonadism 12 with or Without Anosmia 34 0.026
735
c MJR023 Major Affective Disorder 7 33 0.026
736
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.026
737
ALR002 Al-Raqad Syndrome 33 0.026
738
PRS064 Persistent Vegetative State 33 0.026
739
ACT064 Acute Necrotizing Encephalitis 33 0.026
740
c HMF011 Hemifacial Spasm, Familial 33 0.026
741
c MJR003 Major Affective Disorder 6 33 0.026
742
c MJR006 Major Affective Disorder 5 33 0.026
743
TXC020 Toxic Oil Syndrome 33 0.026
744
SGT001 Sagittal Sinus Thrombosis 32 0.026
745
MYC015 Mycobacterium Fortuitum 32 0.026
746
ALP048 Alopecia Totalis 32 0.026
747
HGH041 High-Grade Astrocytoma 32 0.026
748
BLD052 Blood Group Incompatibility 32 0.026
749
INT104 Intravascular Papillary Endothelial Hyperplasia 31 0.026
750
HYP645 Hyperthyroxinemia, Dystransthyretinemic 31 0.026
751
HYP029 Hyperthyroxinemia 31 0.026
752
NRG001 Neurogenic Bowel 31 0.026
753
STT009 Sutton Disease 2 30 0.026
754
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 0.026
755
MNC001 Monocular Esotropia 30 0.026
756
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 30 0.026
757
ISL119 Isolated Optic Neuritis 30 0.026
759
MTY003 Mutyh Polyposis 30 0.026
760
BSL004 Basilar Artery Occlusion 29 0.026
761
ACT228 Acute Radiation Syndrome 29 0.026
762
MYC019 Mycobacterium Marinum 29 0.026
763
c MJR004 Major Affective Disorder 4 28 0.026
765
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.026
766
c HYP518 Hypogonadotropic Hypogonadism 16 with or Without Anosmia 28 0.026
767
HNM002 Hinman Syndrome 27 0.026
768
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 27 0.026
769
CHL079 Children's Interstitial Lung Disease 26 0.026
770
SPC030 Specific Language Disorder 26 0.026
771
FTL073 Fetal Anticonvulsant Syndrome 26 0.026
772
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.026
773
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.026
774
URT049 Urate Oxidase, Pseudogene 25 0.026
775
PRS131 Prostate Cancer/brain Cancer Susceptibility 25 0.026
776
NNT021 Neonatal Meningitis 25 0.026
777
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.026
778
PRT001 Partial Fetal Alcohol Syndrome 24 0.026
779
NCR014 Necrotizing Soft Tissue Infection 23 0.026
780
RGH006 Right Aortic Arch 23 0.026
781
CHR158 Charles Bonnet Syndrome 23 0.026
782
RFS003 Refsum Disease, Infantile Form 22 0.026
783
NNS042 Nonsyndromic Disorders of Testicular Development 21 0.026
784
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 21 0.026
785
BLD165 Blood Group, Colton System 20 0.026
786
BLN008 Blind Hypotensive Eye 18 0.026
787
RTF001 Retiform Hemangioendothelioma 17 0.026
788
INF184 Infective Keratitis 16 0.026
789
BLD137 Blood Group--Ahonen 16 0.026
790
CHR459 Chromosome Xp Deletion 11 0.026
Content
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