Search results for s-adenosylhomocysteine

146 hits were found for s-adenosylhomocysteine

# Family MCID Name MIFTS Score
1
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 27 27.067
2
HYP003 Hypermethioninemia 42 6.901
3
HMC014 Homocysteinemia 54 0.410
4
VCC001 Vaccinia 50 0.324
5
P VSC007 Vascular Disease 65 0.302
6
STM007 Stomatitis 51 0.265
7
P MYP004 Myopathy 63 0.221
8
ADN001 Adenosine Deaminase Deficiency 44 0.221
9
P LVR013 Liver Disease 71 0.205
10
ATH013 Atherosclerosis Susceptibility 68 0.187
11
P NRB010 Neuroblastoma 1 66 0.187
12
IMM167 Immune Deficiency Disease 79 0.167
13
P KDN018 Kidney Disease 73 0.167
14
P HYP265 Hypotonia 43 0.167
15
PYR009 Pyridoxine Deficiency Anemia 32 0.167
16
DFC004 Deficiency Anemia 77 0.145
17
c CHR684 Chronic Kidney Disease 68 0.145
18
END030 End Stage Renal Failure 60 0.145
19
P LYM031 Lymphocytic Leukemia 56 0.145
20
P HMC002 Homocystinuria 52 0.145
21
PRN001 Purine Nucleoside Phosphorylase Deficiency 50 0.145
22
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 28 0.145
23
P ALZ034 Alzheimer Disease 90 0.118
24
CYS001 Cystic Fibrosis 84 0.118
25
c THR092 Thrombophilia Due to Thrombin Defect 74 0.118
26
SVR004 Severe Combined Immunodeficiency 74 0.118
27
HMN044 Human Immunodeficiency Virus Type 1 73 0.118
28
BRK010 Burkitt Lymphoma 68 0.118
29
P LKM062 Leukemia, Acute Lymphoblastic 68 0.118
30
P HRP006 Herpes Simplex 66 0.118
31
LYM017 Lyme Disease 64 0.118
32
P HML002 Hemolytic Anemia 64 0.118
33
ADN018 Adenoma 60 0.118
34
P HRD011 Hereditary Spherocytosis 59 0.118
35
HYP266 Hypoxia 58 0.118
36
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.118
37
CHL014 Cholera 58 0.118
38
PLS011 Plasmacytoma 57 0.118
39
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.118
40
CRN030 Coronary Stenosis 49 0.118
41
ATS010 Autosomal Recessive Disease 49 0.118
42
VTM002 Vitamin B12 Deficiency 48 0.118
43
HLX001 Helix Syndrome 46 0.118
44
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 46 0.118
45
HPT082 Hepatic Adenomas, Familial 40 0.118
46
48X005 48,xyyy 37 0.118
47
PYR016 Pyridoxine Deficiency 31 0.118
48
P CLR023 Colorectal Cancer 100 0.084
49
P HPT023 Hepatocellular Carcinoma 99 0.084
50
ESP021 Esophageal Cancer 90 0.084
51
P GST053 Gastric Cancer 85 0.084
52
P ATX030 Ataxia-Telangiectasia 83 0.084
53
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.084
54
c DLT002 Dilated Cardiomyopathy 81 0.084
55
P RTT002 Rett Syndrome 81 0.084
56
P PRK057 Parkinson Disease, Late-Onset 77 0.084
57
P RSP003 Respiratory Failure 75 0.084
58
GLB002 Glioblastoma 74 0.084
59
PRP027 Peripheral Vascular Disease 72 0.084
60
P PHC003 Pheochromocytoma 71 0.084
61
P LYM118 Lymphoma 70 0.084
62
P LKM002 Leukemia 69 0.084
63
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.084
64
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.084
65
AND002 Androgen Insensitivity Syndrome 66 0.084
66
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.084
67
P ADN016 Adenocarcinoma 65 0.084
68
FCT007 Factor Vii Deficiency 65 0.084
69
CLR108 Colorectal Adenoma 64 0.084
70
ANR007 Anorexia Nervosa 64 0.084
71
P GLM045 Glioma 64 0.084
72
P ANR048 Aniridia 1 64 0.084
73
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.084
74
ACT119 Acute Promyelocytic Leukemia 63 0.084
75
TXC005 Toxic Shock Syndrome 63 0.084
76
FTT001 Fatty Liver Disease 63 0.084
77
ISC004 Ischemia 62 0.084
78
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.084
79
c HPT001 Hepatitis C 62 0.084
80
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.084
81
ACN002 Acanthosis Nigricans 62 0.084
82
NTR005 Nutritional Deficiency Disease 61 0.084
83
LSC001 Lesch-Nyhan Syndrome 61 0.084
84
GLB015 Glioblastoma Multiforme 60 0.084
85
HPT019 Hepatic Encephalopathy 60 0.084
86
P END033 Endocarditis 58 0.084
87
P ALC033 Alcohol Use Disorder 58 0.084
88
P AXN002 Axenfeld-Rieger Syndrome 58 0.084
89
P EXN002 Exanthem 58 0.084
90
LYM027 Lymphopenia 58 0.084
91
YLL002 Yellow Fever 58 0.084
92
IRN002 Iron Metabolism Disease 58 0.084
93
THR024 Thrombosis 58 0.084
94
AGN016 Aging 58 0.084
95
P TRC086 Trichohepatoenteric Syndrome 1 57 0.084
96
P NRP001 Neuropathy 57 0.084
97
P MCR010 Microcephaly 56 0.084
98
PHR003 Pharyngitis 56 0.084
99
P ART021 Arteriosclerosis 56 0.084
100
c MCR113 Microvascular Complications of Diabetes 3 55 0.084
101
CHK001 Chikungunya 55 0.084
102
c ACT020 Acute T Cell Leukemia 54 0.084
103
PNC001 Pancytopenia 54 0.084
104
P MYS005 Myositis 54 0.084
105
P MTR003 Mitral Valve Stenosis 54 0.084
106
P MGL001 Megaloblastic Anemia 54 0.084
107
TLN003 Telangiectasis 53 0.084
108
c ACT134 Acute Liver Failure 53 0.084
109
NNL006 Non-Alcoholic Steatohepatitis 53 0.084
110
CLR109 Colorectal Adenocarcinoma 51 0.084
111
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.084
112
ADR040 Adrenal Gland Pheochromocytoma 51 0.084
113
CRY003 Cryptosporidiosis 50 0.084
114
URM002 Uremia 50 0.084
115
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.084
116
47X002 47,xyy 49 0.084
117
THR013 Thoracic Outlet Syndrome 49 0.084
118
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.084
119
c MCR120 Microvascular Complications of Diabetes 7 48 0.084
120
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 48 0.084
121
GLL048 Glial Tumor 48 0.084
122
IMP004 Impetigo 47 0.084
123
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 47 0.084
124
HMP009 Haemophilus Influenzae 46 0.084
125
TRC003 Trichomoniasis 46 0.084
126
NWC001 Newcastle Disease 45 0.084
127
c MCR130 Microvascular Complications of Diabetes 6 42 0.084
128
c MCR133 Microvascular Complications of Diabetes 4 42 0.084
129
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 42 0.084
130
HPT004 Hepatic Coma 42 0.084
131
AMN002 Amino Acid Metabolic Disorder 42 0.084
132
GLY015 Glycine N-Methyltransferase Deficiency 41 0.084
133
MST004 Mast Cell Neoplasm 40 0.084
134
ADP007 Adie Pupil 40 0.084
135
CHL045 Choline Deficiency Disease 39 0.084
136
ATX010 Ataxia Neuropathy Spectrum 39 0.084
137
EXT007 Extracutaneous Mastocytoma 39 0.084
138
STR077 Streptococcal Toxic-Shock Syndrome 38 0.084
139
c PRG020 Paragangliomas 3 36 0.084
140
ALR002 Al-Raqad Syndrome 32 0.084
141
CKS001 Ck Syndrome 31 0.084
142
MYC088 Mycobacterium Avium Complex Infections 30 0.084
143
P ACT232 Acute Necrotizing Encephalopathy 28 0.084
144
HNM002 Hinman Syndrome 26 0.084
145
AND005 Androgen Insensitivity Syndrome, Mild 20 0.084
146
BLD137 Blood Group--Ahonen 17 0.084
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