Search results for N-Acetylgalactosamine

454 hits were found for N-Acetylgalactosamine

# Family MCID Name MIFTS Score
1
c MCP052 Mucopolysaccharidosis, Type Vi 67 54.794
2
c MCP047 Mucopolysaccharidosis, Type Iva 62 34.950
3
c MCP004 Mucopolysaccharidosis Iv 61 23.421
4
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 23.089
5
c CNG205 Congenital Disorder of Glycosylation, Type Ij 34 16.531
6
MCP033 Mucopolysaccharidoses 44 9.435
7
LYS002 Lysosomal Storage Disease 51 8.738
8
P MRQ003 Morquio Syndrome 35 8.422
9
ATS010 Autosomal Recessive Disease 42 7.381
10
HLX001 Helix Syndrome 48 6.539
11
IGG001 Iga Glomerulonephritis 50 5.888
12
SCH036 Scheie Syndrome 73 4.338
13
P HRP006 Herpes Simplex 65 3.995
14
EXT007 Extracutaneous Mastocytoma 38 3.680
15
MST004 Mast Cell Neoplasm 42 3.680
16
P CHN012 Chondrosarcoma 57 3.372
17
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.317
18
TRT001 Teratocarcinoma 42 3.215
19
P GLM007 Glomerulonephritis 60 3.116
20
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.107
21
P GLC113 Galactosemia I 66 3.023
22
DWR001 Dwarfism 44 3.023
23
GLL048 Glial Tumor 52 2.870
24
GLM045 Glioma 63 2.870
25
CYS001 Cystic Fibrosis 78 2.806
26
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.796
27
TNP004 Tn Polyagglutination Syndrome 42 2.778
28
AMB001 Amebiasis 57 2.736
29
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.717
30
P ADN016 Adenocarcinoma 63 2.717
31
MRQ002 Morquio Syndrome C 13 2.626
32
MLT135 Multiple Sulfatase Deficiency 53 2.510
33
P BRS044 Breast Adenocarcinoma 58 2.479
34
ADN018 Adenoma 59 2.479
35
CLN015 Colon Adenocarcinoma 65 2.479
36
c MCP046 Mucopolysaccharidosis, Type Iiid 50 2.345
37
GLB002 Glioblastoma 67 2.345
38
LNG039 Lung Squamous Cell Carcinoma 57 2.345
39
EMB004 Embryonal Carcinoma 56 2.345
40
SQM006 Squamous Cell Carcinoma 60 2.345
41
LYS030 Lysosomal Storage Disease with Skeletal Involvement 15 2.262
42
DYS018 Dysostosis 44 2.262
43
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 2.220
44
OTT002 Otitis Media 71 2.197
45
PRT251 Proteinuria, Chronic Benign 57 2.197
46
P TYS001 Tay-Sachs Disease 69 2.197
47
48X005 48,xyyy 39 2.197
48
P CLR023 Colorectal Cancer 100 2.029
49
c HYP836 Hypercholesterolemia, Familial, 1 73 2.029
50
P ART021 Arteriosclerosis 54 2.029
51
CYT002 Cytokine Deficiency 43 2.029
52
DYS015 Dysentery 50 1.882
53
CHL014 Cholera 62 1.882
54
P OVR046 Ovarian Cyst 46 1.882
55
P PRS040 Prostate Cancer 95 1.830
56
P FBR017 Fibrosarcoma 56 1.830
57
ACQ007 Acquired Immunodeficiency Syndrome 59 1.830
58
P HRD001 Hereditary Multiple Exostoses 48 1.830
59
HRD104 Hereditary Multiple Osteochondromas 43 1.830
60
P HYP265 Hypotonia 42 1.830
61
c MCP050 Mucopolysaccharidosis, Type Ii 74 1.775
62
P MCL001 Mucolipidosis 49 1.775
63
ODN022 Odontoid Hypoplasia 17 1.775
64
PCT001 Pectus Carinatum 33 1.775
65
c GLC112 Galactosemia Iii 51 1.660
66
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 1.660
67
CHR074 Choriocarcinoma 46 1.660
68
PRP030 Purpura 54 1.660
69
HMP009 Haemophilus Influenzae 41 1.660
70
c BLD146 Blood Group, P1pk System 28 1.570
71
CLR108 Colorectal Adenoma 64 1.570
72
URL001 Urolithiasis 46 1.570
73
ODN023 Odontochondrodysplasia 67 1.570
74
GLC012 Galactosialidosis 56 1.570
75
CRH001 Crohn's Disease 80 1.570
76
P CHR012 Chronic Granulomatous Disease 69 1.570
77
P HMR003 Hemorrhagic Disease 59 1.570
78
HGH043 High Grade Glioma 45 1.570
79
P END044 Endometriosis 62 1.570
80
P ENC018 Encephalopathy 62 1.570
81
DHY008 Dihydroxyadeninuria 24 1.570
82
PPL052 Papillomatosis, Confluent and Reticulated 34 1.537
83
c SYS001 Systemic Lupus Erythematosus 87 1.537
84
ACT098 Acute Erythroid Leukemia 55 1.537
85
P IGN003 Iga Nephropathy 1 39 1.537
86
CLB002 Clubfoot 51 1.537
87
P SCH017 Schindler Disease 37 1.403
88
P PNC035 Pancreatic Cancer 86 1.403
89
CHL065 Cholangiocarcinoma 58 1.403
90
47X002 47,xyy 48 1.403
91
INT079 Intrahepatic Cholangiocarcinoma 51 1.403
92
CYS009 Cystadenoma 43 1.403
93
P KLZ004 Kala-Azar 1 41 1.255
94
P PHC003 Pheochromocytoma 69 1.255
95
HMN044 Human Immunodeficiency Virus Type 1 78 1.255
96
P INF037 Inflammatory Bowel Disease 53 1.255
97
HXS001 Hexosaminidase C 11 1.255
98
LGG001 Legg-Calve-Perthes Disease 60 1.255
99
OST159 Osteogenic Sarcoma 66 1.255
100
ADR040 Adrenal Gland Pheochromocytoma 46 1.255
101
P NRB001 Neuroblastoma 66 1.255
102
PLM014 Pleomorphic Adenoma 51 1.255
103
LSH001 Leishmaniasis 64 1.255
104
P MSC005 Muscular Dystrophy 67 1.255
105
END086 End Stage Renal Disease 52 1.255
106
SVR004 Severe Combined Immunodeficiency 72 1.255
107
c HPT016 Hepatitis B 62 1.255
108
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.255
109
P GNG009 Gangliosidosis 44 1.255
110
SKL017 Skeletal Dysplasias 41 1.087
111
SPN186 Spinal Cord Injury 61 1.087
112
PFF001 Pfeiffer Syndrome 77 1.087
113
c MCP048 Mucopolysaccharidosis, Type Ivb 52 1.087
114
P WSK001 Wiskott-Aldrich Syndrome 72 1.087
115
SND001 Sandhoff Disease 66 1.087
116
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 52 1.087
117
P RHM011 Rheumatoid Arthritis 82 1.087
118
ATM095 Autoimmune Disease 61 1.087
119
KSH004 Kashin-Beck Disease 38 1.087
120
c BRT028 Brittle Cornea Syndrome 1 39 1.087
121
P LKM062 Leukemia, Acute Lymphoblastic 69 1.087
122
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.087
123
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.087
124
MNN047 Mannosidosis, Alpha B, Lysosomal 67 1.087
125
P MTC003 Metachromatic Leukodystrophy 71 1.087
126
SCH069 Schindler Disease, Type I 36 1.087
127
c GLY008 Glycogen Storage Disease Ii 72 1.087
128
c EXS020 Exostoses, Multiple, Type Ii 38 1.087
129
c EXS019 Exostoses, Multiple, Type I 54 1.087
130
P SCL018 Scoliosis 57 1.087
131
P LKD001 Leukodystrophy 59 1.087
132
MDD018 Middle East Respiratory Syndrome 44 1.087
133
P HML001 Hemolytic-Uremic Syndrome 52 1.087
134
VSC003 Visceral Leishmaniasis 55 1.087
135
P VSC011 Vasculitis 61 1.087
136
FTT001 Fatty Liver Disease 62 1.087
137
P THR014 Thrombocytopenia 66 1.087
138
HYP066 Hyperglycemia 61 1.087
139
c HPT001 Hepatitis C 62 1.087
140
HRT012 Heart Valve Disease 53 1.087
141
P ART022 Arthritis 71 1.087
142
ALL029 Allergic Disease 59 1.087
143
c ACT068 Acute Cystitis 61 1.087
144
CRY003 Cryptosporidiosis 56 1.087
145
P HPT021 Hepatitis 69 1.087
146
TTN003 Tetanus 65 1.087
147
P PLY011 Polycystic Ovary Syndrome 57 1.087
148
c GM1007 Gm1 Gangliosidosis 65 1.087
149
c MCP001 Mucopolysaccharidosis Iii 69 1.087
150
CNG065 Congenital Contractures 25 1.087
151
P BRN019 Bernard-Soulier Syndrome 61 0.942
152
P AMY004 Amyloidosis 70 0.942
153
P ATS364 Autism 69 0.887
154
ANX004 Anoxia 40 0.887
155
ALP077 Alpha-Methylacetoacetic Aciduria 52 0.887
156
P MYC084 Mycobacterium Tuberculosis 1 68 0.887
157
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.887
158
P LKM071 Leukemia, Chronic Lymphocytic 75 0.887
159
PLY150 Polykaryocytosis Inducer 29 0.887
160
c LKM063 Leukemia, Chronic Myeloid 71 0.887
161
P SLP006 Sleep Apnea 69 0.887
162
MYL009 Myelodysplastic Syndrome 67 0.887
163
NNL006 Non-Alcoholic Steatohepatitis 54 0.887
164
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.887
165
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.887
166
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.887
167
EXF001 Exfoliation Syndrome 56 0.887
169
NST002 Nestor-Guillermo Progeria Syndrome 35 0.887
170
c ALP105 Alport Syndrome 2, Autosomal Recessive 43 0.887
171
LGN006 Legionnaire Disease 52 0.887
172
KNZ001 Kanzaki Disease 37 0.887
173
MCL075 Macular Dystrophy, Corneal 55 0.887
174
DYG001 Dyggve-Melchior-Clausen Disease 47 0.887
175
c WLM013 Wilms Tumor 1 66 0.887
176
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.887
177
P HPT023 Hepatocellular Carcinoma 96 0.887
178
CLR109 Colorectal Adenocarcinoma 50 0.887
179
GST071 Gastrointestinal Carcinoma 46 0.887
180
BCT022 Bacterial Infectious Disease 56 0.887
181
ARG004 Argyria 26 0.887
182
P ZLL001 Zellweger Syndrome 65 0.887
183
c CHR684 Chronic Kidney Disease 69 0.887
184
ANG016 Angiokeratoma 37 0.887
185
P KDN018 Kidney Disease 72 0.887
186
P MYP004 Myopathy 67 0.887
187
SCR011 Scrapie 39 0.887
188
NTR005 Nutritional Deficiency Disease 61 0.887
189
P RBL001 Rubella 58 0.887
190
KRT006 Keratoconjunctivitis 53 0.887
191
ULC004 Ulcerative Colitis 74 0.887
192
HPT022 Hepatoblastoma 54 0.887
193
P CMM008 Communicating Hydrocephalus 45 0.887
194
P CYS018 Cystitis 59 0.887
195
P OLG002 Oligodendroglioma 66 0.887
196
OVR048 Ovarian Cystadenoma 29 0.887
197
CLR017 Clear Cell Sarcoma 44 0.887
198
PRT036 Peritonitis 65 0.887
199
OST012 Osteoarthritis 77 0.887
200
P PRD008 Periodontitis 64 0.887
201
P MNC007 Monocytic Leukemia 47 0.887
202
P KRT007 Keratoconus 50 0.887
203
P GRF003 Graft-Versus-Host Disease 71 0.887
204
OST003 Osteonecrosis 61 0.887
205
PPL022 Papilloma 53 0.887
206
SQM002 Squamous Cell Papilloma 46 0.887
207
P MLN008 Melanoma 76 0.887
208
P GCH001 Gaucher's Disease 70 0.887
209
TST014 Testicular Cancer 52 0.887
210
SCH014 Schistosomiasis 56 0.887
211
P HYD006 Hydrocephalus 61 0.887
212
P BND020 Bone Disease 59 0.887
213
PST010 Pasteurellosis 39 0.887
214
P RSP003 Respiratory Failure 74 0.887
215
MTR002 Mitral Valve Insufficiency 52 0.887
216
c MLG069 Malignant Hypertension 46 0.887
217
P END033 Endocarditis 58 0.887
218
P PRN023 Prion Disease 60 0.887
219
P RHN004 Rhinitis 57 0.887
220
P PRL003 Proliferative Glomerulonephritis 43 0.887
221
P SLP005 Sleep Disorder 61 0.887
222
GST049 Gastrointestinal System Cancer 49 0.887
223
P CRN025 Corneal Dystrophy 49 0.887
224
P KDN017 Kidney Cancer 61 0.887
225
GST045 Gastroenteritis 58 0.887
226
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.887
227
NWC001 Newcastle Disease 47 0.887
228
NRL005 Neurilemmoma 60 0.887
229
ACT011 Acute Contagious Conjunctivitis 42 0.887
230
P PRP029 Porphyria 60 0.887
231
P URT039 Urticaria 58 0.887
232
P DRR001 Diarrhea 55 0.887
233
RCT020 Rectum Adenocarcinoma 48 0.887
234
STM007 Stomatitis 54 0.887
236
MCL022 Mucolipidoses 33 0.887
237
ALL014 Allergic Encephalomyelitis 34 0.887
238
c GLC111 Galactosemia Ii 50 0.627
239
CLP005 Ciliopathy 41 0.627
240
P PRM011 Primary Ciliary Dyskinesia 69 0.627
241
P OTT001 Otitis Externa 42 0.627
242
MTR087 Maternal Uniparental Disomy 28 0.627
243
SPS057 Spasticity 42 0.627
244
ART140 Arteries, Anomalies of 53 0.627
245
P BLD134 Bladder Cancer 79 0.627
246
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.627
247
PRS129 Prostatic Hyperplasia, Benign 49 0.627
248
c GLL024 Gallbladder Disease 1 52 0.627
249
P MYS003 Myasthenia Gravis 68 0.627
250
INS024 Insulin-Like Growth Factor I 78 0.627
251
SHR107 Short Stature-Obesity Syndrome 25 0.627
252
c SPN398 Spinal Muscular Atrophy, Type Iv 44 0.627
253
SRC027 Sarcoma, Synovial 58 0.627
254
c MCL013 Mucolipidosis Iv 65 0.627
255
FBR012 Fabry Disease 70 0.627
256
c SPR086 Spermatogenic Failure 3 46 0.627
257
ALL003 Allergic Rhinitis 67 0.627
258
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.627
259
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 0.627
260
AGN016 Aging 54 0.627
261
c AGM013 Agammaglobulinemia 1, Autosomal Recessive 37 0.627
262
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.627
263
c LKM070 Leukemia, Acute Monocytic 56 0.627
264
MCR037 Macroglossia 44 0.627
265
P OVR042 Ovarian Cancer 88 0.627
266
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 36 0.627
267
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.627
268
P BRS047 Breast Cancer 98 0.627
269
ALC007 Alcohol Dependence 66 0.627
270
c THR092 Thrombophilia Due to Thrombin Defect 74 0.627
271
WLL001 Williams-Beuren Syndrome 61 0.627
272
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 0.627
273
c CNG415 Congenital Disorder of Glycosylation, Type Ia 59 0.627
274
P CLC063 Celiac Disease 1 66 0.627
275
HYP781 Hypoascorbemia 52 0.627
276
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.627
277
c GLC114 Glaucoma, Primary Closed-Angle 36 0.627
278
P PLM037 Pulmonary Hypertension 72 0.627
279
P BRC003 Brachyolmia 35 0.627
280
P EXN002 Exanthem 58 0.627
281
DFF005 Diffuse Large B-Cell Lymphoma 54 0.627
282
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.627
283
LPP008 Lipoprotein Quantitative Trait Locus 65 0.627
284
DFC004 Deficiency Anemia 74 0.627
285
CVD001 Covid-19 57 0.627
286
P URN019 Urinary Tract Infection 49 0.627
287
INF034 Infective Endocarditis 54 0.627
288
HMN047 Human Cytomegalovirus Infection 57 0.627
289
P SYN012 Synpolydactyly 38 0.627
290
UMB002 Umbilical Hernia 47 0.627
291
BNR002 Bone Resorption Disease 47 0.627
292
P BRC006 Brachydactyly 51 0.627
293
c LKM061 Leukemia, Acute Myeloid 83 0.627
294
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.627
295
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.627
296
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.627
297
c HNT011 Huntington Disease-Like 3 34 0.627
298
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.627
299
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.627
300
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.627
301
PRP083 Porphyria, Acute Intermittent 65 0.627
302
PRT119 Protrusio Acetabuli 33 0.627
303
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 52 0.627
304
MYL069 Myeloma, Multiple 77 0.627
305
c PRD040 Periodontitis, Chronic 52 0.627
306
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.627
307
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.627
308
P CXV002 Coxa Vara 33 0.627
309
FCS014 Fucosidase Regulator 15 0.627
310
IMM165 Immunoglobulin Switch Sequences 14 0.627
311
MST024 Mastocytosis, Cutaneous 67 0.627
312
PCT003 Pectus Excavatum 46 0.627
313
HRW001 Hair Whorl 35 0.627
314
BLD161 Blood Group, Globoside System 38 0.627
315
c PLN021 Peeling Skin Syndrome 3 18 0.627
316
BMB001 Bombay Phenotype 32 0.627
317
GLC003 Glucose Intolerance 54 0.627
318
INT067 Interstitial Nephritis 46 0.627
319
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.627
320
P PLN008 Peeling Skin Syndrome 43 0.627
321
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.627
322
ICH054 Ichthyosis, X-Linked 52 0.627
323
LMY002 Leiomyoma 51 0.627
324
P MTP001 Metaphyseal Dysplasia 38 0.627
325
P CHR285 Chronic Myelomonocytic Leukemia 60 0.627
326
TRM010 Traumatic Brain Injury 51 0.627
327
P LPS004 Lupus Erythematosus 61 0.627
328
CTN007 Cutaneous Leishmaniasis 62 0.627
329
P BCL017 B-Cell Lymphoma 59 0.627
330
P FBR003 Fibrous Histiocytoma 43 0.627
331
P BLD062 Bile Duct Cancer 67 0.627
332
PRS042 Prostate Disease 42 0.627
333
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.627
334
P DYS154 Dystonia 64 0.627
335
OCL006 Ocular Hypertension 53 0.627
336
INT075 Intracranial Hypertension 53 0.627
337
P PSR002 Psoriasis 63 0.627
338
P MYL006 Myeloid Leukemia 61 0.627
339
P HML002 Hemolytic Anemia 62 0.627
340
HMG002 Hemoglobinuria 50 0.627
341
c PLN016 Peeling Skin Syndrome Type a 15 0.627
342
c CHR087 Chronic Cystitis 35 0.627
343
P LVR013 Liver Disease 69 0.627
344
SVR001 Severe Acute Respiratory Syndrome 67 0.627
345
VCC001 Vaccinia 47 0.627
346
SYS004 Systemic Mastocytosis 63 0.627
347
P MST009 Mastocytosis 64 0.627
348
PPL021 Papilledema 49 0.627
349
P GST044 Gastritis 55 0.627
350
GST040 Gastric Adenocarcinoma 67 0.627
351
PLS011 Plasmacytoma 56 0.627
352
P ART023 Arthropathy 61 0.627
353
TRC022 Tricuspid Valve Insufficiency 47 0.627
354
SPN035 Spindle Cell Sarcoma 54 0.627
355
CNN005 Connective Tissue Disease 67 0.627
356
APP008 Appendicitis 62 0.627
357
P RTN016 Retinal Degeneration 52 0.627
358
MYF001 Myofibroma 42 0.627
359
PST011 Pustulosis of Palm and Sole 52 0.627
360
SMN007 Seminoma 42 0.627
361
ANT024 Anthrax Disease 58 0.627
362
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.627
363
PPT005 Peptic Ulcer Disease 58 0.627
364
RDC002 Radiculopathy 52 0.627
365
c CFF010 Coffin-Siris Syndrome 3 42 0.627
366
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.627
367
OST172 Osteochondrodysplasia, Brachydactyly, and Overlapping Malformed Digits 17 0.627
368
P CRN024 Corneal Disease 44 0.627
369
P MMP001 Mumps 57 0.627
370
ANG002 Angiostrongyliasis 46 0.627
371
TNS005 Tonsillitis 57 0.627
372
c PRC016 Pre-Eclampsia 65 0.627
373
BRN028 Brain Cancer 74 0.627
374
P PLM006 Pulmonary Alveolar Proteinosis 53 0.627
375
ALV002 Alveolar Echinococcosis 57 0.627
376
P MLN007 Male Infertility 56 0.627
377
P GLL022 Guillain-Barre Syndrome 60 0.627
378
P LTR001 Lateral Sclerosis 58 0.627
379
PRS021 Prostatic Adenoma 43 0.627
380
c ACT027 Acute Pancreatitis 60 0.627
381
CHN002 Chancroid 36 0.627
382
c MLG084 Malignant Fibrous Histiocytoma 62 0.627
383
P DDN001 Duodenal Ulcer 53 0.627
384
RTN020 Retinal Vascular Disease 46 0.627
385
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.627
386
ORC001 Orchitis 44 0.627
387
P HYP086 Hypothyroidism 69 0.627
388
ECH003 Echinococcosis 53 0.627
389
THR004 Thrombocytosis 53 0.627
390
P CNG003 Congenital Dyserythropoietic Anemia 48 0.627
391
P INT143 Interstitial Cystitis 60 0.627
392
BCT004 Bacteriuria 47 0.627
393
TRN018 Transitional Cell Carcinoma 56 0.627
394
DPH001 Diphtheria 59 0.627
395
DBT008 Diabetic Angiopathy 45 0.627
396
SLV003 Salivary Gland Disease 39 0.627
397
BRC012 Brucellosis 66 0.627
398
SRC014 Sarcoma 65 0.627
399
HNC001 Henoch-Schoenlein Purpura 54 0.627
400
CHL123 Chlamydia 58 0.627
401
PRM013 Premature Menopause 58 0.627
402
BLL004 Bullous Keratopathy 48 0.627
403
PRS045 Prostatic Hypertrophy 53 0.627
404
DSS009 Disseminated Intravascular Coagulation 57 0.627
405
KRT002 Keratomalacia 55 0.627
406
FCH001 Fuchs' Endothelial Dystrophy 50 0.627
407
CNG034 Congestive Heart Failure 69 0.627
408
BRN024 Bronchitis 67 0.627
409
P BRT004 Bartter Disease 58 0.627
410
ATR003 Atrophic Rhinitis 40 0.627
411
P INT068 Intestinal Disease 53 0.627
412
GNG006 Gingival Hypertrophy 36 0.627
413
P INF032 Infertility 57 0.627
414
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.627
415
CRT015 Carotid Artery Occlusion 45 0.627
416
LPD008 Lipid Metabolism Disorder 62 0.627
417
c GM2006 Gm2 Gangliosidosis 46 0.627
418
GLY031 Glycoproteinosis 49 0.627
419
P LPS002 Liposarcoma 64 0.627
420
P MTR014 Motor Neuron Disease 65 0.627
421
c FML021 Familial Hypercholesterolemia 72 0.627
422
ERY004 Erysipelas 47 0.627
423
P ADL010 Adult Respiratory Distress Syndrome 71 0.627
424
LYM021 Lymphadenitis 56 0.627
425
GST023 Gastric Ulcer 52 0.627
426
CHL122 Cholesteatoma of Middle Ear 51 0.627
427
LCH001 Leech Infestation 38 0.627
428
KRT008 Keratopathy 46 0.627
429
P ICH004 Ichthyosis 56 0.627
430
HTR003 Heterotaxy 43 0.627
431
P MNN013 Meningitis 65 0.627
432
XLN247 X-Linked Congenital Retinoschisis 20 0.627
433
ACT200 Acute Monoblastic Leukemia 41 0.627
434
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.627
435
GNR027 Generalized Peeling Skin Syndrome 21 0.627
436
HYD005 Hydrocele 46 0.627
437
P TXP001 Toxoplasmosis 60 0.627
438
HML018 Homologous Wasting Disease 21 0.627
439
P JVN042 Juvenile Retinoschisis 39 0.627
440
c LKM005 Leukemia, T-Cell, Chronic 34 0.627
441
SFT003 Soft Tissue Sarcoma 57 0.627
442
SPL018 Splenomegaly 49 0.627
443
THR035 Thrombasthenia 48 0.627
444
PTT037 Pituitary Tumors 44 0.627
445
BRN071 Brain Injury 50 0.627
446
HYP266 Hypoxia 57 0.627
447
CND006 Candida Glabrata 30 0.627
448
CTN027 Cutaneous Mastocytoma 26 0.627
449
EMB007 Embryonal Sarcoma 40 0.627
450
LYM019 Lymphosarcoma 46 0.627
451
ERY069 Erythrokeratoderma ''en Cocardes'' 27 0.627
452
FBR019 Fibromatosis 42 0.627
453
HPS001 Hip Subluxation 16 0.627
454
MTT004 Metatarsus Adductus 17 0.627
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