Search results for N-Acetylgalactosamine

56 hits were found for N-Acetylgalactosamine

# Family MCID Name MIFTS Score
1
c MCP052 Mucopolysaccharidosis, Type Vi 67 7.359
2
c CNG205 Congenital Disorder of Glycosylation, Type Ij 35 6.514
3
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.526
4
MCP033 Mucopolysaccharidoses 38 0.292
5
HLX001 Helix Syndrome 47 0.273
6
LYS002 Lysosomal Storage Disease 52 0.231
7
P ADN016 Adenocarcinoma 64 0.206
8
IGG001 Iga Glomerulonephritis 48 0.179
9
P BRS047 Breast Cancer 96 0.146
10
P HRP006 Herpes Simplex 65 0.146
11
P GLM045 Glioma 63 0.146
12
c MCP047 Mucopolysaccharidosis, Type Iva 49 0.146
13
AMB001 Amebiasis 49 0.146
14
ATS010 Autosomal Recessive Disease 48 0.146
15
TRT001 Teratocarcinoma 46 0.146
16
GLL048 Glial Tumor 45 0.146
17
TNP004 Tn Polyagglutination Syndrome 40 0.146
18
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.146
19
MST004 Mast Cell Neoplasm 38 0.146
20
EXT007 Extracutaneous Mastocytoma 38 0.146
21
P ALZ034 Alzheimer Disease 88 0.103
22
P PNC035 Pancreatic Cancer 84 0.103
23
GLB015 Glioblastoma Multiforme 75 0.103
24
CRH001 Crohn's Disease 74 0.103
25
c HYP836 Hypercholesterolemia, Familial, 1 72 0.103
26
P NRB001 Neuroblastoma 71 0.103
27
OTT002 Otitis Media 71 0.103
28
MLN008 Melanoma 69 0.103
29
P LVR013 Liver Disease 68 0.103
30
GLC006 Galactosemia 65 0.103
31
LNG039 Lung Squamous Cell Carcinoma 65 0.103
32
CLR108 Colorectal Adenoma 64 0.103
33
CLN015 Colon Adenocarcinoma 63 0.103
34
P END044 Endometriosis 62 0.103
35
P ENC018 Encephalopathy 61 0.103
36
P BRN019 Bernard-Soulier Syndrome 60 0.103
37
ACQ007 Acquired Immunodeficiency Syndrome 60 0.103
38
SQM006 Squamous Cell Carcinoma 60 0.103
39
P BRS044 Breast Adenocarcinoma 59 0.103
40
ADN018 Adenoma 58 0.103
41
EMB004 Embryonal Carcinoma 57 0.103
42
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.103
43
P GLM007 Glomerulonephritis 57 0.103
44
P CHN012 Chondrosarcoma 56 0.103
45
P FBR017 Fibrosarcoma 56 0.103
46
P ART021 Arteriosclerosis 54 0.103
47
P HMR003 Hemorrhagic Disease 52 0.103
48
P HRD001 Hereditary Multiple Exostoses 46 0.103
49
c MLG068 Malignant Glioma 45 0.103
50
BLD161 Blood Group, Globoside System 42 0.103
51
P HYP265 Hypotonia 42 0.103
52
48X005 48,xyyy 39 0.103
53
c HRD104 Hereditary Multiple Osteochondromas 39 0.103
54
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.103
55
c CHR020 Chronic Interstitial Cystitis 37 0.103
56
c BLD146 Blood Group, P1pk System 21 0.103
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