Search results for D-Galactose

432 hits were found for D-Galactose

# Family MCID Name MIFTS Score
1
AGN016 Aging 53 15.391
2
P ANP001 Anaplastic Large Cell Lymphoma 59 3.958
4
P ALZ034 Alzheimer Disease 87 3.566
5
P GLC113 Galactosemia I 65 2.980
6
HLX001 Helix Syndrome 47 2.621
7
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.610
8
P CTR002 Cataract 59 2.564
9
AMN003 Amnestic Disorder 53 2.420
10
P BCL017 B-Cell Lymphoma 57 2.342
11
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.332
12
c CNG411 Congenital Disorder of Glycosylation, Type in 66 2.134
13
P NRB001 Neuroblastoma 66 2.027
14
P GLY013 Glycogen Storage Disease 59 1.981
15
MLD018 Mild Cognitive Impairment 48 1.957
16
c CNG379 Congenital Disorder of Glycosylation, Type It 41 1.883
17
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.883
18
PRM013 Premature Menopause 57 1.845
19
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.791
20
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.778
21
P OST002 Osteoporosis 76 1.778
22
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.778
23
LVR012 Liver Cirrhosis 62 1.679
24
P DMN002 Dementia 65 1.671
25
P HPT023 Hepatocellular Carcinoma 95 1.545
26
INS024 Insulin-Like Growth Factor I 77 1.544
27
PRM329 Premature Aging 36 1.509
28
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.507
29
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.466
30
ARG004 Argyria 26 1.397
31
LPD008 Lipid Metabolism Disorder 61 1.371
32
FTT001 Fatty Liver Disease 61 1.371
33
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.342
34
GLB002 Glioblastoma 67 1.310
35
ACT098 Acute Erythroid Leukemia 55 1.310
36
c PCH010 Pachyonychia Congenita 3 43 1.274
37
P INF032 Infertility 60 1.274
38
48X005 48,xyyy 39 1.232
39
DBT007 Diabetic Cataract 36 1.182
40
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.182
41
HYP066 Hyperglycemia 60 1.182
42
P PRD008 Periodontitis 63 1.161
43
HYP266 Hypoxia 56 1.161
44
SRN001 Serine Deficiency 24 1.139
45
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 1.139
46
ANX010 Anxiety 70 1.116
47
P PNC035 Pancreatic Cancer 87 1.116
48
BRK010 Burkitt Lymphoma 65 1.092
49
P GLM040 Glioma Susceptibility 1 70 1.092
50
MLG169 Malignant Astrocytoma 57 1.092
51
c BRN108 Branchiootic Syndrome 1 63 1.065
52
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.065
53
LYM019 Lymphosarcoma 46 1.065
54
c ACT134 Acute Liver Failure 57 1.065
55
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.037
56
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.037
57
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.037
58
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.037
59
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.037
60
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.037
61
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.037
62
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.037
63
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.037
64
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.037
65
BNR002 Bone Resorption Disease 47 1.037
66
HYP060 Hyperinsulinism 53 1.037
67
BRN004 Brain Edema 54 1.037
68
CLN015 Colon Adenocarcinoma 64 1.005
69
SPL018 Splenomegaly 47 1.005
70
P RTN024 Retinoblastoma 72 0.969
71
HYP017 Hypophosphatemia 49 0.969
72
FBR012 Fabry Disease 71 0.969
73
c CNT035 Central Nervous System Disease 53 0.969
74
P ADN016 Adenocarcinoma 63 0.969
75
P LVR013 Liver Disease 68 0.969
76
P GLL022 Guillain-Barre Syndrome 59 0.969
77
CRB039 Cerebrovascular Disease 65 0.969
78
P INF038 Influenza 68 0.969
79
P NRV007 Nervous System Disease 65 0.969
80
ATR055 Atrial Septal Aneurysm 23 0.969
81
P KLZ004 Kala-Azar 1 41 0.927
82
ADN018 Adenoma 58 0.927
83
P RHB003 Rhabdomyosarcoma 66 0.927
84
LSH001 Leishmaniasis 63 0.927
85
PRT251 Proteinuria, Chronic Benign 58 0.913
86
c FCL025 Focal Segmental Glomerulosclerosis 1 49 0.913
87
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.913
88
ANT039 Antisynthetase Syndrome 55 0.913
89
P NPH012 Nephrotic Syndrome 61 0.913
90
P FCL005 Focal Segmental Glomerulosclerosis 57 0.913
91
c CNG188 Congenital Disorder of Glycosylation, Type if 37 0.878
92
SXL003 Sexual Disorder 49 0.871
93
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.871
94
P BLD134 Bladder Cancer 79 0.871
95
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.871
96
c OPT053 Optic Atrophy 1 62 0.871
97
c ATM089 Autoimmune Neuropathy 28 0.871
98
GST023 Gastric Ulcer 52 0.871
99
IMP005 Impotence 52 0.871
100
P MLN007 Male Infertility 56 0.871
101
P PLY011 Polycystic Ovary Syndrome 57 0.871
102
P PTT006 Pituitary Adenoma 55 0.871
103
TST015 Testicular Disease 42 0.871
104
P OVR046 Ovarian Cyst 43 0.871
105
PTT037 Pituitary Tumors 44 0.871
106
BRN071 Brain Injury 50 0.871
107
P TRM003 Tremor 50 0.871
108
PST092 Posttransplant Acute Limbic Encephalitis 29 0.871
109
P HPT021 Hepatitis 68 0.737
110
c NNS007 Nonsyndromic Deafness 36 0.737
111
c MCR115 Microvascular Complications of Diabetes 5 65 0.502
112
CHL014 Cholera 62 0.464
113
CYS001 Cystic Fibrosis 77 0.424
114
HYP056 Hypoglycemia 65 0.402
115
P OVR042 Ovarian Cancer 88 0.379
116
P FBR017 Fibrosarcoma 55 0.379
117
c GM1007 Gm1 Gangliosidosis 65 0.379
118
P GNG009 Gangliosidosis 44 0.379
119
P HVY001 Heavy Chain Disease 32 0.355
121
CLF027 Cleft Palate, Isolated 64 0.355
122
PRT036 Peritonitis 65 0.355
123
47X002 47,xyy 47 0.355
124
P MSC005 Muscular Dystrophy 66 0.355
125
RNL077 Renal Fibrosis 46 0.328
126
P LCT002 Lactose Intolerance 51 0.328
127
P CYS018 Cystitis 58 0.328
128
PPL052 Papillomatosis, Confluent and Reticulated 34 0.300
129
P URN019 Urinary Tract Infection 48 0.300
130
END062 Endometrial Hyperplasia 47 0.300
131
CHG001 Chagas Disease 65 0.300
132
PRT037 Pertussis 49 0.300
133
SLP001 Sleeping Sickness 56 0.300
134
STN013 Stenotrophomonas Maltophilia Infection 26 0.300
135
P LKM062 Leukemia, Acute Lymphoblastic 69 0.268
136
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.268
137
P MYS005 Myositis 55 0.268
138
PRP030 Purpura 54 0.268
139
BCT022 Bacterial Infectious Disease 55 0.268
140
GST045 Gastroenteritis 58 0.268
141
P INT143 Interstitial Cystitis 59 0.268
142
c ACT068 Acute Cystitis 60 0.268
143
CYT002 Cytokine Deficiency 43 0.268
144
MYX011 Myxozoa 18 0.268
145
c GLC111 Galactosemia Ii 54 0.232
146
P CLR023 Colorectal Cancer 100 0.232
147
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.232
148
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.232
149
ENT011 Enterocolitis 55 0.232
150
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.232
151
WRN001 Werner Syndrome 69 0.232
152
TBL029 Tubulin, Beta 28 0.232
153
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.232
154
HRN029 Hearing Loss, Noise-Induced 37 0.232
155
INC002 Inclusion Body Myositis 56 0.232
156
P SNS001 Sensorineural Hearing Loss 60 0.232
157
DPH001 Diphtheria 59 0.232
158
P DRR001 Diarrhea 55 0.232
159
P ALC033 Alcohol Use Disorder 67 0.232
160
c HPT016 Hepatitis B 62 0.232
161
PST011 Pustulosis of Palm and Sole 52 0.232
162
P GST044 Gastritis 55 0.232
163
TRT001 Teratocarcinoma 41 0.232
164
P BRS044 Breast Adenocarcinoma 58 0.232
165
GST033 Gestational Diabetes 60 0.232
166
GLC003 Glucose Intolerance 53 0.232
167
P VNW001 Von Willebrand's Disease 64 0.232
168
GT001 Gout 63 0.232
169
SKN016 Skin Disease 63 0.232
170
P MYT002 Myotonic Dystrophy 51 0.232
171
P PSR002 Psoriasis 63 0.232
172
GLM045 Glioma 62 0.232
173
P HYP098 Hypereosinophilic Syndrome 66 0.232
174
ANX004 Anoxia 40 0.232
175
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 18 0.232
176
GLL048 Glial Tumor 51 0.232
177
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.190
178
c GLC115 Galactosemia Iv 23 0.190
179
c PRG020 Paragangliomas 3 39 0.190
180
P LYM118 Lymphoma 66 0.190
181
OCL069 Ocular Motor Apraxia 57 0.190
182
PLY150 Polykaryocytosis Inducer 29 0.190
183
c GLC112 Galactosemia Iii 51 0.190
184
MSC157 Muscular Dystrophy, Duchenne Type 78 0.190
185
ALC007 Alcohol Dependence 65 0.190
186
OST159 Osteogenic Sarcoma 66 0.190
187
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.190
188
AND002 Androgen Insensitivity Syndrome 63 0.190
189
HYP457 Hypertrophic Scars 42 0.190
190
DSS032 Disease by Infectious Agent 55 0.190
191
c MCR133 Microvascular Complications of Diabetes 4 41 0.190
192
c MCR113 Microvascular Complications of Diabetes 3 52 0.190
193
c MCR130 Microvascular Complications of Diabetes 6 41 0.190
194
c MCR120 Microvascular Complications of Diabetes 7 47 0.190
195
c THY107 Thymoma, Familial 42 0.190
196
P CHN012 Chondrosarcoma 56 0.190
197
c CNG389 Congenital Disorder of Glycosylation, Type Iim 49 0.190
198
c HRM007 Hermansky-Pudlak Syndrome 4 46 0.190
199
P MYC007 Myocardial Infarction 69 0.190
200
P MJR001 Major Depressive Disorder 68 0.190
201
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.190
202
c CNG383 Congenital Disorder of Glycosylation, Type Iik 43 0.190
203
P ASP006 Aspergillosis 71 0.190
204
P HNT016 Huntington Disease 73 0.190
205
HMN044 Human Immunodeficiency Virus Type 1 76 0.190
206
FRC013 Fructose Utilization 15 0.190
207
INV001 Invasive Aspergillosis 48 0.190
208
NNL006 Non-Alcoholic Steatohepatitis 54 0.190
209
PTN001 Patent Foramen Ovale 61 0.190
210
P LKM002 Leukemia 65 0.190
211
PHR003 Pharyngitis 57 0.190
212
KRT008 Keratopathy 46 0.190
213
P GCH001 Gaucher's Disease 69 0.190
214
P THY023 Thymoma 64 0.190
215
EXC002 Exocrine Pancreatic Insufficiency 42 0.190
216
STR103 Streptococcus Pneumonia 47 0.190
217
NTR005 Nutritional Deficiency Disease 60 0.190
218
ISC004 Ischemia 61 0.190
219
P HRT032 Heart Disease 84 0.190
220
LYM017 Lyme Disease 63 0.190
221
MDD018 Middle East Respiratory Syndrome 44 0.190
222
P END033 Endocarditis 58 0.190
223
TYP007 Typhoid Fever 63 0.190
224
IGG001 Iga Glomerulonephritis 50 0.190
225
CNS004 Constipation 56 0.190
226
P SYP003 Syphilis 59 0.190
227
GNG013 Gingivitis 59 0.190
228
SHW001 Shwartzman Phenomenon 36 0.190
229
LYS002 Lysosomal Storage Disease 51 0.190
230
P PNC044 Pancreatitis 61 0.190
231
c ACT027 Acute Pancreatitis 60 0.190
232
GRD001 Giardiasis 46 0.190
233
CMP034 Complete Androgen Insensitivity Syndrome 55 0.190
234
TXC005 Toxic Shock Syndrome 61 0.190
235
MNT002 Mental Depression 56 0.190
236
PLR005 Pleuropneumonia 33 0.190
237
CYS005 Cysticercosis 60 0.190
238
P KRT007 Keratoconus 49 0.190
239
DYS015 Dysentery 49 0.190
240
HPT004 Hepatic Coma 43 0.190
241
P MLN008 Melanoma 75 0.190
242
P ART022 Arthritis 70 0.190
243
c INH020 Inherited Metabolic Disorder 47 0.190
244
DCB001 Decubitus Ulcer 61 0.190
245
P TRC031 Trichorhinophalangeal Syndrome 37 0.190
246
P BRN022 Bronchiectasis 59 0.190
247
SKN019 Skin Melanoma 70 0.190
248
ULC004 Ulcerative Colitis 74 0.190
249
CRH001 Crohn's Disease 80 0.190
250
DRT002 Duarte Variant Galactosemia 13 0.190
251
SLC037 Slc35a2-Congenital Disorder of Glycosylation 12 0.190
252
P HRP006 Herpes Simplex 65 0.190
253
ACT168 Acute Annular Outer Retinopathy 10 0.190
254
PRN071 Parenteral Nutrition-Associated Cholestasis 23 0.190
255
DPR016 Depression 64 0.190
256
P CHR345 Chronic Pain 50 0.190
257
P ENC018 Encephalopathy 62 0.190
258
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.190
259
INF034 Infective Endocarditis 53 0.134
260
CLT003 Colitis 63 0.134
261
3MC003 3mc Syndrome 49 0.134
262
P CRD119 Cardiac Arrest 68 0.134
263
c STC013 Stickler Syndrome, Type Ii 36 0.134
264
VLL006 Villous Adenoma 40 0.134
265
P INF037 Inflammatory Bowel Disease 53 0.134
266
ART140 Arteries, Anomalies of 52 0.134
267
ATH013 Atherosclerosis Susceptibility 63 0.134
268
P CLC063 Celiac Disease 1 65 0.134
269
ART001 Arterial Tortuosity Syndrome 64 0.134
270
P MDL005 Medulloblastoma 75 0.134
271
OTT002 Otitis Media 70 0.134
272
c TYP009 Type 2 Diabetes Mellitus 91 0.134
273
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.134
274
RNL024 Renal Glucosuria 60 0.134
275
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.134
276
PRK076 Porokeratosis 2, Palmar, Plantar, and Disseminated Type 26 0.134
277
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.134
278
FCS002 Fucosidosis 61 0.134
279
c GM1004 Gm1-Gangliosidosis, Type I 59 0.134
280
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.134
281
c MCP050 Mucopolysaccharidosis, Type Ii 73 0.134
282
c STC015 Stickler Syndrome, Type I 50 0.134
283
c TYR012 Tyrosinemia, Type I 61 0.134
284
P BRS047 Breast Cancer 97 0.134
285
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 36 0.134
286
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.134
287
LPP008 Lipoprotein Quantitative Trait Locus 65 0.134
288
HYP025 Hyperphosphatemia 47 0.134
289
ATS010 Autosomal Recessive Disease 42 0.134
290
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 0.134
291
GLC022 Glucose/galactose Malabsorption 45 0.134
292
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.134
293
SPR020 Superficial Mycosis 34 0.134
294
P SPP010 Suppressor of Tumorigenicity 3 50 0.134
295
VLV047 Volvulus of Midgut 55 0.134
296
KRT019 Keratitis, Hereditary 66 0.134
297
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.134
298
c GLL024 Gallbladder Disease 1 53 0.134
299
c LKM063 Leukemia, Chronic Myeloid 70 0.134
300
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.134
301
P DNG005 Dengue Virus 55 0.134
302
EPD055 Epidermolysis Bullosa, Nonspecific, Autosomal Recessive 27 0.134
303
MLD001 Melioidosis 67 0.134
304
CHL065 Cholangiocarcinoma 57 0.134
305
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.134
306
ATM095 Autoimmune Disease 61 0.134
307
P LKM071 Leukemia, Chronic Lymphocytic 74 0.134
308
CRT072 Creutzfeldt-Jakob Disease 67 0.134
309
HRW001 Hair Whorl 35 0.134
310
CRV035 Cervical Cancer 72 0.134
311
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 0.134
312
OST017 Osteomyelitis 63 0.134
313
THY128 Thyroid Tumor 33 0.134
314
INV018 Invasive Mole 22 0.134
315
RBS001 Rabies 57 0.134
316
CHL123 Chlamydia 58 0.134
317
FCH001 Fuchs' Endothelial Dystrophy 48 0.134
318
P PLY041 Polymyositis 58 0.134
319
HMR023 Hemorrhagic Cystitis 43 0.134
320
CLR109 Colorectal Adenocarcinoma 50 0.134
321
BLL004 Bullous Keratopathy 48 0.134
322
P HYP069 Hyperparathyroidism 62 0.134
323
P MXL015 Maxillary Sinusitis 37 0.134
324
SPH010 Sphingolipidosis 47 0.134
325
P HMN010 Hemangioma 61 0.134
326
LNG037 Lung Sarcoma 28 0.134
327
HST010 Histiocytosis 49 0.134
328
P BNG095 Benign Giant Cell Tumor 43 0.134
329
RTN020 Retinal Vascular Disease 45 0.134
330
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.134
331
c MLG084 Malignant Fibrous Histiocytoma 62 0.134
332
CHL068 Cholestasis 61 0.134
333
P SPN046 Spinal Muscular Atrophy 62 0.134
334
P ECL001 Eclampsia 52 0.134
335
OVR047 Ovarian Cystadenocarcinoma 38 0.134
336
BLD044 Bladder Disease 48 0.134
337
MST004 Mast Cell Neoplasm 41 0.134
338
P CRV031 Cervical Adenocarcinoma 48 0.134
339
ANT019 Anterograde Amnesia 38 0.134
340
CNJ007 Conjunctivochalasis 38 0.134
341
TST018 Testicular Yolk Sac Tumor 38 0.134
342
TRN015 Transient Cerebral Ischemia 62 0.134
343
P LTR001 Lateral Sclerosis 57 0.134
344
P HYP086 Hypothyroidism 68 0.134
345
P CND004 Candidiasis 57 0.134
346
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.134
347
P OVR049 Ovarian Disease 50 0.134
348
BRC012 Brucellosis 66 0.134
349
P EHL001 Ehlers-Danlos Syndrome 57 0.134
350
P PLY019 Polyneuropathy 52 0.134
351
P GLM007 Glomerulonephritis 59 0.134
352
P CPL006 Capillary Hemangioma 53 0.134
353
CRV040 Cervix Carcinoma 50 0.134
354
CVR006 Cavernous Hemangioma 51 0.134
355
P AGN002 Agnosia 53 0.134
356
P MYP004 Myopathy 67 0.134
357
SPN035 Spindle Cell Sarcoma 51 0.134
358
MLK006 Milk Allergy 47 0.134
359
NCR001 Necrotizing Ulcerative Gingivitis 26 0.134
360
P PRK001 Porokeratosis 54 0.134
361
CYS014 Cystadenocarcinoma 51 0.134
362
c SCN007 Secondary Hyperparathyroidism 50 0.134
363
GST010 Gestational Trophoblastic Neoplasm 52 0.134
364
EXT007 Extracutaneous Mastocytoma 38 0.134
365
INT079 Intrahepatic Cholangiocarcinoma 51 0.134
366
ALL029 Allergic Disease 61 0.134
367
ASP003 Aseptic Meningitis 50 0.134
368
LST001 Listeriosis 59 0.134
369
DBT008 Diabetic Angiopathy 47 0.134
370
P FNC004 Fanconi Syndrome 60 0.134
371
MST005 Mastitis 52 0.134
372
P ART005 Arteriovenous Malformation 64 0.134
373
PRC002 Paracoccidioidomycosis 53 0.134
374
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.134
375
URL001 Urolithiasis 45 0.134
376
c PRC016 Pre-Eclampsia 64 0.134
377
P MCR010 Microcephaly 59 0.134
378
ORL005 Oral Candidiasis 55 0.134
379
P HML001 Hemolytic-Uremic Syndrome 52 0.134
380
HNC001 Henoch-Schoenlein Purpura 56 0.134
381
SRC014 Sarcoma 64 0.134
382
CRB004 Cerebral Artery Occlusion 45 0.134
383
SHG001 Shigellosis 61 0.134
384
TLN003 Telangiectasis 51 0.134
385
HLL004 Hellp Syndrome 53 0.134
386
P END039 Endodermal Sinus Tumor 42 0.134
387
SCR011 Scrapie 39 0.134
388
MYS001 Myositis Ossificans 44 0.134
389
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.134
390
CHR074 Choriocarcinoma 46 0.134
391
PLG002 Plague 58 0.134
392
BRN024 Bronchitis 67 0.134
393
HPT022 Hepatoblastoma 54 0.134
394
ANT024 Anthrax Disease 57 0.134
395
P MYL006 Myeloid Leukemia 60 0.134
396
P FBR003 Fibrous Histiocytoma 43 0.134
397
P SLP003 Salpingitis 39 0.134
398
KLD004 Keloid Disorder 38 0.134
399
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.134
400
P MRQ003 Morquio Syndrome 36 0.134
401
P TYR004 Tyrosinemia 49 0.134
402
VSC003 Visceral Leishmaniasis 54 0.134
403
c ACT075 Acute Myocardial Infarction 55 0.134
404
P MSC003 Muscular Atrophy 52 0.134
405
IMP004 Impetigo 48 0.134
406
OST012 Osteoarthritis 77 0.134
407
FND002 Fundus Dystrophy 54 0.134
408
P CHL066 Cholangitis 51 0.134
409
VSC002 Vascular Dementia 59 0.134
410
ALL014 Allergic Encephalomyelitis 34 0.134
411
P HMP007 Hemophilia 52 0.134
412
GST050 Gastrointestinal System Disease 55 0.134
413
HMP009 Haemophilus Influenzae 41 0.134
414
PLM052 Pulmonary Arteriovenous Malformation 43 0.134
415
P SZR006 Seizure Disorder 69 0.134
416
P AMY004 Amyloidosis 69 0.134
417
KRT006 Keratoconjunctivitis 53 0.134
418
P ACT105 Acute Mountain Sickness 52 0.134
419
P PRG139 Progeroid Syndrome 30 0.134
420
c INH030 Inherited Retinal Disorder 28 0.134
421
PRQ002 Paraquat Poisoning 28 0.134
422
ACT181 Acute Motor Axonal Neuropathy 25 0.134
423
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.134
424
MST020 Mast Cell Activation Syndrome 27 0.134
425
NNT021 Neonatal Meningitis 22 0.134
426
PYG006 Pyogenic Granuloma 36 0.134
427
THR035 Thrombasthenia 48 0.134
428
CRB086 Cerebral Aneurysms 40 0.134
429
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.134
430
P OVR082 Overgrowth Syndrome 41 0.134
431
THY029 Thyroid Carcinoma 55 0.134
432
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.134
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