Search results for Molybdenum

608 hits were found for Molybdenum

# Family MCID Name MIFTS Score
1
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 47 54.029
2
MLY001 Molybdenum Cofactor Deficiency 40 50.090
3
MLY009 Molybdenum Cofactor Deficiency, Complementation Group B 39 49.548
4
MLY010 Molybdenum Cofactor Deficiency, Complementation Group C 41 48.678
5
SLF012 Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency 10 21.167
6
SLF014 Sulfite Oxidase Deficiency, Isolated 53 8.084
7
P XNT004 Xanthinuria 37 4.944
8
c INH020 Inherited Metabolic Disorder 47 4.793
9
c HRD142 Hereditary Xanthinuria 43 3.941
10
c XNT010 Xanthinuria, Type I 52 3.743
11
ATS010 Autosomal Recessive Disease 42 3.700
12
P ENC018 Encephalopathy 62 3.441
13
c XNT011 Xanthinuria, Type Ii 37 3.145
14
c MCR312 Microphthalmia, Syndromic 10 39 3.114
15
ENC005 Encephalomalacia 43 2.998
16
P MCR010 Microcephaly 59 2.887
17
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.780
18
HRW001 Hair Whorl 35 2.780
19
DNT012 Dental Caries 53 2.747
20
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.703
21
c PLM127 Pulmonary Hypertension, Primary, 3 34 2.608
22
GT001 Gout 63 2.422
23
WLS001 Wilson Disease 70 2.355
24
48X005 48,xyyy 39 2.293
25
CNT047 Contact Dermatitis 57 2.269
26
DRM006 Dermatitis 62 2.269
27
P SZR006 Seizure Disorder 69 2.269
28
IRN002 Iron Metabolism Disease 56 2.239
29
P HYP097 Hyperekplexia 62 2.235
30
P HMC002 Homocystinuria 52 1.887
31
P ATS364 Autism 72 1.824
32
c PLM121 Pulmonary Hypertension, Primary, 4 28 1.775
33
ALL029 Allergic Disease 61 1.742
34
EPL131 Epilepsy, Pyridoxine-Dependent 45 1.701
35
BCT022 Bacterial Infectious Disease 56 1.691
36
P EPL164 Epilepsy 70 1.689
37
P DYS154 Dystonia 64 1.620
38
ESP021 Esophageal Cancer 84 1.585
39
P HYP265 Hypotonia 42 1.556
40
P CRB088 Cerebral Atrophy 33 1.542
41
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.440
42
VSL002 Visual Epilepsy 39 1.440
43
RCK004 Rickets 65 1.433
44
P PNM006 Pneumoconiosis 55 1.408
45
ANT018 Anthracosis 51 1.408
46
MTL002 Metal Metabolism Disorder 30 1.394
47
MTB004 Metabolic Acidosis 48 1.392
48
CRB037 Cerebral Palsy 67 1.392
49
AGN016 Aging 54 1.390
50
HLX001 Helix Syndrome 47 1.379
51
P ISL078 Isolated Ectopia Lentis 58 1.364
52
DFC004 Deficiency Anemia 74 1.364
53
ANX004 Anoxia 40 1.364
54
DND001 Dandy-Walker Syndrome 49 1.356
55
ASP024 Asparagine Synthetase Deficiency 37 1.356
56
SPS057 Spasticity 43 1.348
57
FTT001 Fatty Liver Disease 61 1.344
58
P DRR001 Diarrhea 55 1.331
59
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.317
60
P LTR001 Lateral Sclerosis 58 1.317
61
P PRK039 Parkinsonism 55 1.309
62
PYL006 Pyloric Stenosis 48 1.309
63
ALK013 Alkaptonuria 58 1.288
64
HYP550 Hypomagnesemia 1, Intestinal 45 1.288
65
BRN024 Bronchitis 67 1.276
66
CYT002 Cytokine Deficiency 43 1.276
67
HMP005 Hemiplegia 53 1.255
68
LRN003 Learning Disability 49 1.255
69
OST012 Osteoarthritis 77 1.251
70
PHN003 Phenylketonuria 76 1.246
71
P DRM053 Dermatitis, Atopic 65 1.236
72
NTR005 Nutritional Deficiency Disease 60 1.236
73
P INB001 Inborn Amino Acid Metabolism Disorder 10 1.236
74
AMN012 Aminoacidopathies 19 1.236
75
AMN002 Amino Acid Metabolic Disorder 38 1.236
76
BTN003 Biotinidase Deficiency 62 1.228
77
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.204
78
P SCH015 Schizophrenia 74 1.187
79
ADN018 Adenoma 58 1.181
80
LNG031 Lung Benign Neoplasm 51 1.181
81
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 1.137
82
PPL022 Papilloma 53 1.120
83
SQM002 Squamous Cell Papilloma 45 1.120
84
HMP009 Haemophilus Influenzae 41 1.120
85
P LRG012 Large Congenital Melanocytic Nevus 47 1.115
86
ADP007 Adie Pupil 40 1.115
87
MLN065 Melanocytic Nevus Syndrome, Congenital 61 1.115
88
PRN024 Purine-Pyrimidine Metabolic Disorder 25 1.115
89
HNM002 Hinman Syndrome 26 1.115
90
GTR002 Goiter 52 1.100
91
GST033 Gestational Diabetes 61 1.080
92
P SKN015 Skin Carcinoma 71 1.080
93
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.080
94
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 1.070
95
LSC001 Lesch-Nyhan Syndrome 62 1.070
96
P ALZ034 Alzheimer Disease 87 1.057
97
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.057
98
SPS004 Spastic Quadriplegia 39 1.057
99
QDR001 Quadriplegia 49 1.057
100
HYP266 Hypoxia 56 1.057
101
CLF001 Cleft Lip 54 1.057
102
HYP264 Hypertonia 36 1.057
103
c ATS007 Autism Spectrum Disorder 72 1.051
104
HYP014 Hyperuricemia 51 1.044
105
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.033
106
ACT084 Acute Stress Disorder 53 1.033
107
PST028 Post-Traumatic Stress Disorder 59 1.033
108
P LCT001 Lactic Acidosis 50 1.033
109
TXC002 Toxic Encephalopathy 51 1.033
110
CLF004 Cleft Lip/palate 57 1.033
111
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 1.024
112
P MYC084 Mycobacterium Tuberculosis 1 68 1.007
113
P HNT016 Huntington Disease 73 0.976
114
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.976
115
P INF038 Influenza 68 0.976
116
MTL005 Metal Allergy 39 0.976
117
BNR002 Bone Resorption Disease 47 0.959
118
PPL052 Papillomatosis, Confluent and Reticulated 34 0.959
119
HVY002 Heavy Metal Poisoning 22 0.943
120
P OVR042 Ovarian Cancer 88 0.941
121
MWT001 Mowat-Wilson Syndrome 57 0.941
122
SLC006 Silicosis 55 0.941
123
P PLM036 Pulmonary Fibrosis 65 0.941
124
PLG002 Plague 58 0.941
125
P BRS047 Breast Cancer 97 0.927
126
IRN001 Iron Deficiency Anemia 58 0.927
127
c HYP248 Hyperprolinemia, Type I 43 0.911
128
CRB150 Cerebral Creatine Deficiency Syndrome 2 54 0.911
129
MLT018 Multiple Carboxylase Deficiency 45 0.911
130
P ART022 Arthritis 70 0.909
131
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.894
132
c ATR087 Atrial Standstill 1 74 0.872
133
P DMN002 Dementia 65 0.872
134
c CNT035 Central Nervous System Disease 53 0.872
135
DGN001 Degenerative Disc Disease 48 0.872
136
P NRV007 Nervous System Disease 66 0.872
137
c GLL024 Gallbladder Disease 1 53 0.851
138
ANG054 Angina Pectoris 65 0.851
139
c TYP008 Type 1 Diabetes Mellitus 77 0.851
140
LNG099 Lung Disease 62 0.851
141
ADN001 Adenosine Deaminase Deficiency 59 0.840
142
RTR008 Root Resorption 44 0.838
143
PPL058 Papilloma of Choroid Plexus 54 0.829
144
P INF032 Infertility 60 0.829
145
THY030 Thyroid Gland Disease 50 0.829
146
P HYP086 Hypothyroidism 69 0.829
147
P BRS044 Breast Adenocarcinoma 58 0.829
148
URL001 Urolithiasis 45 0.805
149
c SYS001 Systemic Lupus Erythematosus 86 0.805
150
KLB003 Klebsiella Pneumonia 49 0.805
151
P MLN007 Male Infertility 56 0.805
152
P LPS004 Lupus Erythematosus 61 0.805
153
WST001 West Syndrome 64 0.804
154
SRC014 Sarcoma 64 0.781
155
SPN035 Spindle Cell Sarcoma 51 0.781
156
HMN044 Human Immunodeficiency Virus Type 1 76 0.778
157
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.778
158
c VRL010 Viral Hepatitis 52 0.778
159
LVR012 Liver Cirrhosis 62 0.778
160
HMS001 Hemosiderosis 48 0.778
161
PRM236 Primary Biliary Cholangitis 62 0.778
162
DYS073 Dysphagia 53 0.778
163
P MTC069 Mitochondrial Disorders 57 0.778
164
P RRH023 Rare Hereditary Hemochromatosis 53 0.778
165
P OVR082 Overgrowth Syndrome 42 0.778
166
P CRB045 Cerebellar Hypoplasia 40 0.757
167
c HYP699 Hyperekplexia 1 44 0.757
168
ORT008 Orotic Aciduria 56 0.757
169
PRT112 Portal Hypertension, Noncirrhotic 29 0.748
170
P MLT020 Multiple Sclerosis 79 0.748
171
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.748
172
P ANP001 Anaplastic Large Cell Lymphoma 61 0.748
173
P PNT019 Pontocerebellar Hypoplasia 45 0.748
174
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.748
175
P PRS040 Prostate Cancer 95 0.712
176
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.712
177
P MJR001 Major Depressive Disorder 68 0.712
178
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.712
179
c MJR024 Major Affective Disorder 9 40 0.712
180
BLC012 Bile Acid Malabsorption, Primary 43 0.712
181
c MJR022 Major Affective Disorder 8 37 0.712
182
P ALC033 Alcohol Use Disorder 67 0.712
183
TRC013 Trichostrongylosis 21 0.712
184
MNT002 Mental Depression 56 0.712
185
P HYP061 Hypertrophic Cardiomyopathy 69 0.712
186
P AGN002 Agnosia 53 0.712
187
INT066 Interstitial Lung Disease 60 0.712
188
P BPL003 Bipolar Disorder 56 0.712
189
MDD011 Mood Disorder 62 0.712
190
BRS051 Breast Disease 58 0.712
191
PPL002 Papillary Carcinoma 46 0.712
192
DPR016 Depression 65 0.712
193
P CTR002 Cataract 59 0.712
194
STM007 Stomatitis 52 0.712
195
ORL011 Oral Cancer 60 0.712
196
P HPT023 Hepatocellular Carcinoma 95 0.699
197
P LVR013 Liver Disease 68 0.699
198
INS024 Insulin-Like Growth Factor I 77 0.665
199
c BRN108 Branchiootic Syndrome 1 63 0.665
200
P FML340 Familial Episodic Pain Syndrome 50 0.665
201
ORL015 Oral Squamous Cell Carcinoma 43 0.665
202
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.665
203
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.665
204
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 35 0.665
205
HND015 Hand Skill, Relative 29 0.665
206
P HYP009 Hypertrophic Pyloric Stenosis 41 0.665
207
CMP034 Complete Androgen Insensitivity Syndrome 55 0.665
208
BRN004 Brain Edema 54 0.665
209
CHL067 Cholecystitis 59 0.665
210
SQM006 Squamous Cell Carcinoma 59 0.665
211
END028 Endemic Goiter 36 0.665
212
NWC001 Newcastle Disease 48 0.665
213
P FBR017 Fibrosarcoma 55 0.665
214
VCC001 Vaccinia 49 0.665
215
GLM045 Glioma 62 0.665
216
OVR094 Ovarian Epithelial Cancer 39 0.665
217
GLL048 Glial Tumor 52 0.665
218
SNL007 Senile Cataract 40 0.665
219
P PNM007 Pneumonia 64 0.665
220
CPP004 Copper Deficiency Myelopathy 28 0.665
221
ORL004 Oral Submucous Fibrosis 56 0.665
222
SPN186 Spinal Cord Injury 61 0.665
223
MYC017 Mycobacterium Kansasii 36 0.665
224
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 0.665
225
CYN003 Cyanide Poisoning 21 0.665
226
NRM022 Neurometabolic Disease 23 0.665
227
ACT181 Acute Motor Axonal Neuropathy 25 0.665
228
NNL006 Non-Alcoholic Steatohepatitis 54 0.652
229
ALL010 Allergic Contact Dermatitis 56 0.652
230
P PNC035 Pancreatic Cancer 86 0.652
231
HYP005 Hypokalemia 55 0.652
232
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.644
233
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.644
234
DHY011 Dihydropyrimidinase Deficiency 44 0.644
235
c HYP597 Hyperprolinemia, Type Ii 43 0.644
236
PPL049 Papillon-Lefevre Syndrome 65 0.644
237
PYR035 Pyrimidine Metabolic Disorder 25 0.644
238
HYP351 Hypertrichosis Universalis Congenita, Ambras Type 35 0.644
239
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.644
240
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 0.644
241
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.644
242
SPS003 Spastic Diplegia 52 0.644
243
RDN001 Reading Disorder 40 0.644
244
ART002 Arts Syndrome 66 0.644
245
XLN215 X-Linked Congenital Generalized Hypertrichosis 16 0.644
246
ANC002 Anca-Associated Vasculitis 44 0.644
247
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.644
248
c PCH010 Pachyonychia Congenita 3 43 0.552
249
MLD001 Melioidosis 67 0.552
250
P GLM040 Glioma Susceptibility 1 70 0.552
251
PNC001 Pancytopenia 52 0.552
252
MLG169 Malignant Astrocytoma 57 0.552
253
P PRP019 Peripheral Nervous System Disease 57 0.552
254
P VSC011 Vasculitis 61 0.552
255
ADL002 Adult Syndrome 69 0.539
256
ART140 Arteries, Anomalies of 52 0.539
257
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.539
258
DWN001 Down Syndrome 70 0.539
259
c PRM196 Premature Ovarian Failure 1 58 0.539
260
LPP008 Lipoprotein Quantitative Trait Locus 65 0.539
261
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.539
262
PRM013 Premature Menopause 57 0.539
263
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.539
264
HYP781 Hypoascorbemia 52 0.539
265
P NJM001 Nijmegen Breakage Syndrome 75 0.539
266
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.539
267
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.539
268
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.539
269
VTM033 Vitamin K Deficiency Bleeding 50 0.539
270
P BNC003 Bone Cancer 58 0.539
271
PTH002 Pathological Gambling 48 0.539
272
ISC004 Ischemia 61 0.539
273
c ACT027 Acute Pancreatitis 60 0.539
274
P PNC044 Pancreatitis 61 0.539
275
KRT002 Keratomalacia 54 0.539
276
CRT017 Cartilage Disease 52 0.539
277
INT002 Intermittent Claudication 61 0.539
278
P TRN020 Turner Syndrome 67 0.539
279
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.539
280
P CRN300 Coronary Heart Disease 1 73 0.539
281
CRN020 Coronary Restenosis 39 0.539
282
P MRC003 Mercury Poisoning 48 0.539
283
ATX019 Ataxia with Vitamin E Deficiency 44 0.539
284
CRH001 Crohn's Disease 80 0.539
285
P MTR014 Motor Neuron Disease 65 0.539
286
P VSC018 Visceral Steatosis 32 0.539
287
c NRB010 Neuroblastoma 1 60 0.471
288
MTH071 Methane Production 25 0.391
289
CRD005 Cardia Cancer 38 0.319
290
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.277
291
P GST053 Gastric Cancer 82 0.277
292
P LNG032 Lung Cancer 98 0.277
293
SMT007 Smith-Fineman-Myers Syndrome 32 0.277
294
NRL016 Neural Tube Defects 81 0.252
295
c TYP009 Type 2 Diabetes Mellitus 92 0.226
296
ADN022 Adenylosuccinase Deficiency 44 0.226
297
PCT003 Pectus Excavatum 43 0.226
298
PLM001 Pulmonary Tuberculosis 69 0.226
299
CRB039 Cerebrovascular Disease 65 0.226
300
URM002 Uremia 47 0.226
301
c HPT016 Hepatitis B 62 0.226
302
END086 End Stage Renal Disease 54 0.226
303
47X002 47,xyy 48 0.226
304
NNT049 Nontuberculous Mycobacterial Lung Disease 46 0.226
305
c HMC039 Hemochromatosis, Type 1 73 0.196
306
AST006 Astigmatism 46 0.196
307
KSH001 Keshan Disease 31 0.196
308
GLC003 Glucose Intolerance 53 0.196
309
PLY150 Polykaryocytosis Inducer 29 0.196
310
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.196
311
P SCL018 Scoliosis 57 0.196
312
P GLL020 Gallbladder Disease 57 0.196
313
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.196
314
c SCL052 Scleroderma, Familial Progressive 60 0.196
315
LTN004 Late-Onset Retinal Degeneration 60 0.196
316
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.196
317
P PRN023 Prion Disease 60 0.196
318
P HPT021 Hepatitis 68 0.196
319
HYP006 Hypertensive Heart Disease 48 0.196
320
SKN016 Skin Disease 62 0.196
321
HST010 Histiocytosis 49 0.196
322
P GLL018 Gallbladder Cancer 53 0.196
323
CRB086 Cerebral Aneurysms 40 0.196
324
CHR028 Chronic Wasting Disease 33 0.196
325
c CHR684 Chronic Kidney Disease 74 0.196
326
P BRN022 Bronchiectasis 59 0.196
327
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.160
328
P AST005 Asthma 76 0.160
329
P SPP010 Suppressor of Tumorigenicity 3 51 0.160
330
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.160
331
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.160
332
HMC014 Homocysteinemia 52 0.160
333
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.160
334
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.160
335
GLY010 Glycine Encephalopathy 57 0.160
336
MND025 Mandibulofacial Dysostosis with Alopecia 39 0.160
337
P KRT007 Keratoconus 50 0.160
338
P SHR001 Short Bowel Syndrome 53 0.160
339
MCR013 Microphthalmia 60 0.160
340
PRT013 Portal Hypertension 59 0.160
341
P LKD001 Leukodystrophy 58 0.160
342
P HYP078 Hypertrophy of Breast 41 0.160
343
c SPN225 Spondyloarthropathy 1 70 0.160
344
VSC053 Visceral Steatosis, Congenital 35 0.160
345
ENT011 Enterocolitis 55 0.160
346
ADR040 Adrenal Gland Pheochromocytoma 45 0.160
347
P EXN002 Exanthem 58 0.160
348
STT041 Stuttering 52 0.160
349
STR103 Streptococcus Pneumonia 47 0.160
350
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.160
351
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.160
352
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.160
353
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.160
354
RFL001 Reflex Sympathetic Dystrophy 51 0.160
355
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.160
356
c HYP836 Hypercholesterolemia, Familial, 1 73 0.160
357
ATM095 Autoimmune Disease 61 0.160
358
P PHC003 Pheochromocytoma 70 0.160
359
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.160
360
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.160
361
c LVR030 Liver Failure, Infantile, Transient 34 0.160
362
P FRG001 Fragile X Syndrome 70 0.160
363
SMT004 Smith-Lemli-Opitz Syndrome 69 0.160
364
ANN002 Anencephaly 57 0.160
365
P RSP003 Respiratory Failure 74 0.160
366
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 55 0.160
367
IGR001 Ige Responsiveness, Atopic 59 0.160
368
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.160
369
BRN014 Bronchopneumonia 52 0.160
370
CHL068 Cholestasis 61 0.160
371
GLB002 Glioblastoma 67 0.160
372
LPD008 Lipid Metabolism Disorder 61 0.160
373
SPN051 Spondylitis 51 0.160
374
ALG001 Algoneurodystrophy 37 0.160
375
P OBS001 Obstructive Jaundice 49 0.160
376
INF009 Inflammatory Spondylopathy 30 0.160
377
DPH001 Diphtheria 59 0.160
378
P ADL010 Adult Respiratory Distress Syndrome 71 0.160
379
P NRV006 Nervous System Cancer 47 0.160
380
ART016 Aortic Aneurysm 69 0.160
381
ACR005 Acrodermatitis 38 0.160
382
STR067 Stroke, Ischemic 79 0.160
383
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.160
384
OST016 Osteochondrosis 52 0.160
385
HYP056 Hypoglycemia 65 0.160
386
HYP141 Hyperphenylalaninemia 42 0.160
387
P DBT009 Diabetes Mellitus 67 0.160
388
PRN019 Perinatal Necrotizing Enterocolitis 60 0.160
389
ENT007 Enteropathica 24 0.160
390
BNG077 Benign Idiopathic Neonatal Seizures 22 0.160
391
P BLD134 Bladder Cancer 79 0.113
392
P SRC025 Sarcoidosis 1 70 0.113
393
CYS001 Cystic Fibrosis 77 0.113
394
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 0.113
395
P MTC003 Metachromatic Leukodystrophy 71 0.113
396
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 61 0.113
397
HLC007 Helicobacter Pylori Infection 67 0.113
398
FRY006 Fryns Microphthalmia Syndrome 52 0.113
399
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.113
400
c MCP047 Mucopolysaccharidosis, Type Iva 62 0.113
401
c MCP049 Mucopolysaccharidosis, Type Vii 62 0.113
402
MYL005 Myelofibrosis 70 0.113
403
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.113
405
c MCR133 Microvascular Complications of Diabetes 4 41 0.113
406
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.113
407
TRN021 Transaldolase Deficiency 43 0.113
408
PRP001 Propionic Acidemia 65 0.113
409
WST005 West Nile Virus 55 0.113
410
CHK001 Chikungunya 60 0.113
411
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.113
412
P PLM037 Pulmonary Hypertension 69 0.113
413
CNT057 Central Centrifugal Cicatricial Alopecia 36 0.113
414
P ASP001 Asperger Syndrome 48 0.113
415
ART035 Arterial Calcification of Infancy 58 0.113
416
c MGL028 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 24 0.113
417
DSS032 Disease by Infectious Agent 55 0.113
418
MLD018 Mild Cognitive Impairment 48 0.113
419
OST003 Osteonecrosis 61 0.113
420
PNM005 Pneumonic Plague 47 0.113
421
INT067 Interstitial Nephritis 47 0.113
422
GRD001 Giardiasis 46 0.113
423
AMB002 Amblyopia 49 0.113
424
NSP002 Nasopharyngitis 45 0.113
425
c PRC016 Pre-Eclampsia 64 0.113
426
FBR009 Fibrous Dysplasia 48 0.113
427
INT395 Intracranial Meningioma 48 0.113
428
TBL035 Tubulinopathy 34 0.113
429
SPP007 Suppression Amblyopia 38 0.113
430
P PRK057 Parkinson Disease, Late-Onset 79 0.113
431
P OST002 Osteoporosis 77 0.113
432
ATH013 Atherosclerosis Susceptibility 63 0.113
433
P GLC113 Galactosemia I 65 0.113
434
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.113
435
P KRB001 Krabbe Disease 69 0.113
436
P LPR021 Leprosy 3 71 0.113
437
CYS019 Cystathioninuria 46 0.113
438
HMC038 Hemochromatosis, Neonatal 33 0.113
439
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.113
440
P CLC063 Celiac Disease 1 66 0.113
441
HYD038 Hydrops Fetalis, Nonimmune 57 0.113
442
JMP002 Jumping Frenchmen of Maine 21 0.113
443
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.113
444
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.113
445
DCT002 Ductal Carcinoma in Situ 58 0.113
446
P ERL057 Early Infantile Epileptic Encephalopathy 61 0.113
447
HYP017 Hypophosphatemia 49 0.113
448
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.113
449
c LYM150 Lymphatic Malformation 7 43 0.113
450
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.113
451
PHS021 Phosphoglycerate Dehydrogenase Deficiency 46 0.113
452
SCK003 Sickle Cell Anemia 74 0.113
453
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.113
454
ENC055 Encephalopathy, Ethylmalonic 51 0.113
455
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.113
456
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.113
457
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.113
458
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.113
459
P KLZ004 Kala-Azar 1 41 0.113
460
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.113
461
P DVL012 Developmental Dysplasia of the Hip 1 45 0.113
462
c PNC108 Pancreatitis, Hereditary 68 0.113
463
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.113
464
PMP006 Pemphigus Vulgaris, Familial 58 0.113
465
CLF027 Cleft Palate, Isolated 64 0.113
466
EPT021 Epithelial Recurrent Erosion Dystrophy 46 0.113
467
EXF001 Exfoliation Syndrome 56 0.113
468
c MCR113 Microvascular Complications of Diabetes 3 52 0.113
469
c MCR130 Microvascular Complications of Diabetes 6 41 0.113
470
c MCR120 Microvascular Complications of Diabetes 7 47 0.113
471
PNT009 Pontine Tegmental Cap Dysplasia 34 0.113
472
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.113
473
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.113
474
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 0.113
475
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.113
476
ALX003 Alexander Disease 61 0.113
477
c DVL034 Developmental and Epileptic Encephalopathy 3 45 0.113
478
CMP063 Complement Factor B Deficiency 31 0.113
479
BLL004 Bullous Keratopathy 47 0.113
480
BRC012 Brucellosis 66 0.113
481
P BND020 Bone Disease 60 0.113
482
P URN019 Urinary Tract Infection 49 0.113
483
CLT003 Colitis 63 0.113
484
HYP003 Hypermethioninemia 51 0.113
485
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.113
486
SPC010 Speech and Communication Disorders 48 0.113
487
PRP027 Peripheral Vascular Disease 71 0.113
488
c ACT073 Acute Leukemia 59 0.113
489
DYS015 Dysentery 50 0.113
490
CMP002 Campylobacteriosis 50 0.113
491
MST005 Mastitis 52 0.113
492
c ACT068 Acute Cystitis 61 0.113
493
BRS007 Breast Malignant Phyllodes Tumor 45 0.113
494
P ADN016 Adenocarcinoma 63 0.113
495
URT010 Ureteral Obstruction 45 0.113
496
PRP016 Paraplegia 52 0.113
497
P MVM001 Movement Disease 61 0.113
498
TBL003 Tubular Adenocarcinoma 40 0.113
499
P CNJ013 Conjunctivitis 66 0.113
500
SVR004 Severe Combined Immunodeficiency 71 0.113
501
CMD001 Comedo Carcinoma 37 0.113
502
ANK001 Ankylosis 51 0.113
503
KRT008 Keratopathy 46 0.113
504
P CRN037 Craniosynostosis 67 0.113
505
MCR017 Macrocytic Anemia 44 0.113
506
HYP080 Hypogonadism 49 0.113
507
P GLL022 Guillain-Barre Syndrome 59 0.113
508
BRN028 Brain Cancer 73 0.113
509
NNT010 Nontoxic Goiter 32 0.113
510
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.113
511
PLR005 Pleuropneumonia 33 0.113
512
P THR014 Thrombocytopenia 66 0.113
513
LYM021 Lymphadenitis 56 0.113
514
P DDN001 Duodenal Ulcer 53 0.113
515
OCL022 Ocular Melanoma 54 0.113
516
P HYP035 Hypophosphatasia 61 0.113
517
DMP001 Dumping Syndrome 43 0.113
518
TXC005 Toxic Shock Syndrome 62 0.113
519
P BNG013 Benign Breast Phyllodes Tumor 35 0.113
520
DBT007 Diabetic Cataract 35 0.113
521
TNC003 Tinea Corporis 39 0.113
522
FLR002 Filariasis 55 0.113
523
KHN001 Kuhnt-Junius Degeneration 48 0.113
524
ASB001 Asbestosis 47 0.113
525
CHL004 Cholelithiasis 48 0.113
526
LPN001 Louping Ill 27 0.113
527
GNG003 Gingival Recession 50 0.113
528
PTS001 Patau Syndrome 55 0.113
529
CNT033 Central Nervous System Cancer 47 0.113
530
TST014 Testicular Cancer 51 0.113
531
ERL001 Early Myoclonic Encephalopathy 63 0.113
532
P GLY013 Glycogen Storage Disease 59 0.113
533
BRN009 Burning Mouth Syndrome 51 0.113
534
TNC002 Tinea Capitis 42 0.113
535
HYP066 Hyperglycemia 60 0.113
536
P ART023 Arthropathy 60 0.113
537
P TMP001 Temporal Lobe Epilepsy 49 0.113
538
MMM001 Mammary Paget's Disease 53 0.113
539
LYS002 Lysosomal Storage Disease 51 0.113
540
MNK001 Menkes Disease 64 0.113
541
PYR037 Pyruvate Carboxylase Deficiency 45 0.113
542
P NSP012 Nasopharyngeal Carcinoma 60 0.113
543
DRV001 Dravet Syndrome 70 0.113
544
LYS012 Lysosomal Acid Lipase Deficiency 64 0.113
545
ADR007 Adrenoleukodystrophy 74 0.113
546
MNN043 Meningioma, Familial 79 0.113
547
ANR040 Aneurysm 60 0.113
548
P SYS005 Systemic Scleroderma 73 0.113
549
P GST044 Gastritis 55 0.113
550
GST045 Gastroenteritis 58 0.113
551
DNT001 Dental Fluorosis 42 0.113
552
OBS082 Obstructive Nephropathy 41 0.113
553
PLR022 Pleural Disease 45 0.113
554
TMP006 Temporomandibular Ankylosis 19 0.113
555
P THL005 Thalassemia 56 0.113
556
P INS002 in Situ Carcinoma 53 0.113
557
P THY032 Thyroiditis 56 0.113
558
P TRM003 Tremor 50 0.113
559
P LCH002 Lichen Planus 55 0.113
560
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 18 0.113
561
AVN001 Avian Influenza 61 0.113
562
SCR001 Secretory Meningioma 40 0.113
563
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.113
564
MLT001 Multiple Chemical Sensitivity 38 0.113
565
c BRS049 Breast Carcinoma in Situ 50 0.113
566
VSC002 Vascular Dementia 59 0.113
567
RTR011 Retroperitoneal Fibrosis 47 0.113
568
MCP033 Mucopolysaccharidoses 44 0.113
569
CHR178 Chromosomal Triplication 34 0.113
570
BRN056 Bronchopulmonary Dysplasia 57 0.113
571
ADR022 Adrenomyeloneuropathy 39 0.113
572
LSH001 Leishmaniasis 63 0.113
573
PRT036 Peritonitis 65 0.113
574
DRM011 Dermatophytosis 52 0.113
575
P AMY004 Amyloidosis 69 0.113
576
GST039 Gastroduodenitis 37 0.113
577
c LCL006 Localized Scleroderma 64 0.113
578
GST050 Gastrointestinal System Disease 55 0.113
579
P ALP008 Alopecia 53 0.113
580
SLC035 Slc39a14 Deficiency 8 0.113
581
INT040 Intrinsic Asthma 36 0.113
582
KRT006 Keratoconjunctivitis 53 0.113
583
ALL006 Allergic Asthma 56 0.113
584
ETN001 Eating Disorder 59 0.113
585
DHY008 Dihydroxyadeninuria 24 0.113
586
PCT001 Pectus Carinatum 33 0.113
587
ORL013 Oral Lichen Planus 45 0.113
588
HNS001 Hansen's Disease 32 0.113
589
NNN007 Non-Involuting Congenital Hemangioma 40 0.113
590
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.113
591
P ZLL001 Zellweger Syndrome 65 0.113
592
PRX001 Peroxisomal Disease 46 0.113
593
PTY002 Pityriasis Versicolor 37 0.113
594
CTN007 Cutaneous Leishmaniasis 61 0.113
595
P PMP001 Pemphigus 55 0.113
596
P TYR004 Tyrosinemia 49 0.113
597
PRS115 Prosthetic Joint Infection 42 0.113
598
PST092 Posttransplant Acute Limbic Encephalitis 29 0.113
599
CLF056 Cleft Lip with or Without Cleft Palate 43 0.113
600
ASB003 Asbestos Intoxication 32 0.113
601
ART109 Arterial Thoracic Outlet Syndrome 24 0.113
602
P AVS003 Avascular Necrosis 41 0.113
603
OST115 Osteonecrosis of the Jaw 40 0.113
604
GRN033 Granulomatous Mastitis 31 0.113
605
RHM015 Rhombencephalosynapsis 29 0.113
606
CRD137 Cardiogenic Shock 56 0.113
607
CLS049 Classic Phenylketonuria 42 0.113
608
THY029 Thyroid Carcinoma 54 0.113
Content
Loading form....