Search results for xylose

125 hits were found for xylose

# Family MCID Name MIFTS Score
1
P CLC063 Celiac Disease 1 66 0.271
2
P OVR082 Overgrowth Syndrome 50 0.262
3
P DRR001 Diarrhea 55 0.221
4
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.178
5
P CTR002 Cataract 60 0.156
6
ALC007 Alcohol Dependence 66 0.148
7
P INT068 Intestinal Disease 53 0.140
8
IRR002 Irritable Bowel Syndrome 65 0.131
9
LVR012 Liver Cirrhosis 62 0.131
10
TRP004 Tropical Sprue 41 0.131
11
GRD001 Giardiasis 45 0.121
12
GST050 Gastrointestinal System Disease 56 0.111
13
ANX004 Anoxia 40 0.111
14
P ANP001 Anaplastic Large Cell Lymphoma 58 0.099
15
BLN006 Blind Loop Syndrome 37 0.099
16
c THY056 Thyroid Dyshormonogenesis 3 30 0.099
17
DRM006 Dermatitis 61 0.086
18
ACQ007 Acquired Immunodeficiency Syndrome 60 0.086
19
CNS004 Constipation 58 0.086
20
BCT022 Bacterial Infectious Disease 56 0.086
21
ENT011 Enterocolitis 51 0.086
22
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.086
23
48X005 48,xyyy 39 0.086
24
FCS014 Fucosidase Regulator 15 0.086
25
IMM167 Immune Deficiency Disease 78 0.070
26
CRH001 Crohn's Disease 74 0.070
27
P KDN018 Kidney Disease 72 0.070
28
DFC004 Deficiency Anemia 70 0.070
29
PLM001 Pulmonary Tuberculosis 69 0.070
30
P LVR013 Liver Disease 68 0.070
31
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.070
32
TYP007 Typhoid Fever 63 0.070
33
P ART023 Arthropathy 62 0.070
34
HYP066 Hyperglycemia 61 0.070
35
GST045 Gastroenteritis 59 0.070
36
P URT039 Urticaria 58 0.070
37
P EHL001 Ehlers-Danlos Syndrome 58 0.070
38
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.070
39
c GRV008 Graves Disease 1 56 0.070
40
c EXS019 Exostoses, Multiple, Type I 53 0.070
41
PRN011 Pernicious Anemia 53 0.070
42
c VRL010 Viral Hepatitis 52 0.070
43
DYS015 Dysentery 52 0.070
44
HLX001 Helix Syndrome 47 0.070
45
CHR074 Choriocarcinoma 47 0.070
46
P PLL002 Pellagra 46 0.070
47
DMP001 Dumping Syndrome 44 0.070
48
c EXS020 Exostoses, Multiple, Type Ii 40 0.070
49
c ACT004 Acute Diarrhea 39 0.070
50
c THY071 Thyroid Dyshormonogenesis 1 31 0.070
51
PST092 Posttransplant Acute Limbic Encephalitis 29 0.070
52
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.049
53
c LKM061 Leukemia, Acute Myeloid 84 0.049
54
CYS001 Cystic Fibrosis 81 0.049
55
P RHM011 Rheumatoid Arthritis 80 0.049
56
OST012 Osteoarthritis 78 0.049
57
P ART022 Arthritis 69 0.049
58
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.049
59
P LPR021 Leprosy 3 69 0.049
60
P SYS005 Systemic Scleroderma 68 0.049
61
GST092 Gastroesophageal Reflux 67 0.049
62
P HPT021 Hepatitis 67 0.049
63
c MGR028 Migraine with or Without Aura 1 67 0.049
64
P MSC005 Muscular Dystrophy 66 0.049
65
HYP056 Hypoglycemia 66 0.049
66
P DRM053 Dermatitis, Atopic 66 0.049
67
c DBT099 Diabetes Mellitus, Type I 65 0.049
68
PLG002 Plague 63 0.049
69
LPD008 Lipid Metabolism Disorder 62 0.049
70
CLT003 Colitis 62 0.049
71
ATM095 Autoimmune Disease 62 0.049
72
FTT001 Fatty Liver Disease 61 0.049
73
P MYL006 Myeloid Leukemia 60 0.049
74
P VNT002 Ventricular Septal Defect 60 0.049
75
LNG099 Lung Disease 60 0.049
76
P ATR010 Atrial Heart Septal Defect 60 0.049
77
PRT013 Portal Hypertension 59 0.049
78
PPT005 Peptic Ulcer Disease 59 0.049
79
c ACT073 Acute Leukemia 58 0.049
80
ISC004 Ischemia 58 0.049
81
P HDC001 Headache 57 0.049
82
FLR002 Filariasis 55 0.049
83
GST037 Gastroparesis 54 0.049
84
PRT038 Protein-Energy Malnutrition 54 0.049
85
KRT006 Keratoconjunctivitis 53 0.049
86
CRH005 Crohn's Colitis 53 0.049
87
FDL002 Food Allergy 51 0.049
88
ILS001 Ileus 51 0.049
89
CCC002 Coccidiosis 51 0.049
90
ASC010 Ascaris Lumbricoides Infection 50 0.049
91
HRT011 Heart Septal Defect 50 0.049
92
VLV047 Volvulus of Midgut 49 0.049
93
47X002 47,xyy 49 0.049
94
SPL018 Splenomegaly 48 0.049
95
MLK006 Milk Allergy 48 0.049
96
CLN019 Colonic Disease 47 0.049
97
PRD004 Prediabetes Syndrome 47 0.049
98
P HRD001 Hereditary Multiple Exostoses 46 0.049
99
GLC022 Glucose/galactose Malabsorption 45 0.049
100
RSP021 Respiratory Allergy 45 0.049
101
TNS007 Taeniasis 45 0.049
102
PNT038 Peanut Allergy 45 0.049
103
FNG004 Fungal Meningitis 44 0.049
104
MYX004 Myxedema 43 0.049
105
ANC001 Ancylostomiasis 43 0.049
106
MST004 Mast Cell Neoplasm 42 0.049
107
EXC002 Exocrine Pancreatic Insufficiency 42 0.049
108
INT046 Intestinal Tuberculosis 41 0.049
109
c HRD104 Hereditary Multiple Osteochondromas 39 0.049
110
DBT007 Diabetic Cataract 38 0.049
111
EXT007 Extracutaneous Mastocytoma 38 0.049
112
c ALP005 Alpha Chain Disease 37 0.049
113
ASC001 Ascaridiasis 35 0.049
114
HNS001 Hansen's Disease 34 0.049
115
c EHL076 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1 34 0.049
116
P PRG139 Progeroid Syndrome 28 0.049
117
c ALP087 Alpha-Heavy Chain Disease 28 0.049
118
MTH071 Methane Production 26 0.049
119
INT043 Intestinal Disaccharidase Deficiency 26 0.049
120
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.049
121
ADS015 Aids Wasting Syndrome 22 0.049
123
c IMR003 Imerslund-Grasbeck Syndrome 2 21 0.049
124
OCL016 Ocular Albinism, X-Linked 18 0.049
125
ACT168 Acute Annular Outer Retinopathy 10 0.049
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