Search results for s-adenosylhomocysteine

144 hits were found for s-adenosylhomocysteine

# Family MCID Name MIFTS Score
1
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 29 27.061
2
HYP003 Hypermethioninemia 40 6.898
3
HMC014 Homocysteinemia 53 0.405
4
VCC001 Vaccinia 49 0.320
5
P VSC007 Vascular Disease 63 0.298
6
STM007 Stomatitis 50 0.261
7
P MYP004 Myopathy 70 0.219
8
ADN001 Adenosine Deaminase Deficiency 47 0.219
9
P LVR013 Liver Disease 68 0.202
10
P HYP265 Hypotonia 43 0.202
11
P NRB001 Neuroblastoma 72 0.185
12
ATH013 Atherosclerosis Susceptibility 65 0.185
13
IMM167 Immune Deficiency Disease 78 0.165
14
P KDN018 Kidney Disease 72 0.165
15
PYR009 Pyridoxine Deficiency Anemia 34 0.165
16
DFC004 Deficiency Anemia 70 0.143
17
c CHR684 Chronic Kidney Disease 70 0.143
18
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.143
19
LYM017 Lyme Disease 64 0.143
20
PRN001 Purine Nucleoside Phosphorylase Deficiency 55 0.143
21
P HMC002 Homocystinuria 53 0.143
22
END086 End Stage Renal Disease 51 0.143
23
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 32 0.143
24
P ALZ034 Alzheimer Disease 88 0.117
25
CYS001 Cystic Fibrosis 81 0.117
26
SVR004 Severe Combined Immunodeficiency 73 0.117
27
c THR092 Thrombophilia Due to Thrombin Defect 73 0.117
28
HMN044 Human Immunodeficiency Virus Type 1 71 0.117
29
P LKM062 Leukemia, Acute Lymphoblastic 69 0.117
30
BRK010 Burkitt Lymphoma 67 0.117
31
P HRP006 Herpes Simplex 65 0.117
32
P HML002 Hemolytic Anemia 63 0.117
33
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.117
34
P HRD011 Hereditary Spherocytosis 60 0.117
35
P MCR010 Microcephaly 59 0.117
36
CHL014 Cholera 59 0.117
37
ADN018 Adenoma 59 0.117
38
HYP266 Hypoxia 57 0.117
39
PLS011 Plasmacytoma 56 0.117
40
CRN030 Coronary Stenosis 50 0.117
41
ATS010 Autosomal Recessive Disease 48 0.117
42
VTM002 Vitamin B12 Deficiency 48 0.117
43
HLX001 Helix Syndrome 47 0.117
44
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 47 0.117
45
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.117
46
48X005 48,xyyy 39 0.117
47
PYR016 Pyridoxine Deficiency 30 0.117
48
P HPT023 Hepatocellular Carcinoma 100 0.083
49
P CLR023 Colorectal Cancer 99 0.083
50
ESP021 Esophageal Cancer 90 0.083
51
P GST053 Gastric Cancer 83 0.083
52
P ATX030 Ataxia-Telangiectasia 82 0.083
53
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.083
54
P RTT002 Rett Syndrome 80 0.083
55
c DLT002 Dilated Cardiomyopathy 79 0.083
56
P PRK057 Parkinson Disease, Late-Onset 78 0.083
57
P RSP003 Respiratory Failure 74 0.083
58
P PHC003 Pheochromocytoma 71 0.083
59
PRP027 Peripheral Vascular Disease 71 0.083
60
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.083
61
P LKM002 Leukemia 68 0.083
62
FCT007 Factor Vii Deficiency 67 0.083
63
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.083
64
AND002 Androgen Insensitivity Syndrome 66 0.083
65
CLR108 Colorectal Adenoma 64 0.083
66
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.083
67
P ADN016 Adenocarcinoma 64 0.083
68
P GLM045 Glioma 63 0.083
69
P ANR048 Aniridia 1 63 0.083
70
c MLG084 Malignant Fibrous Histiocytoma 63 0.083
71
ACT119 Acute Promyelocytic Leukemia 63 0.083
72
ANR007 Anorexia Nervosa 63 0.083
73
c HPT001 Hepatitis C 62 0.083
74
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.083
75
P TRC086 Trichohepatoenteric Syndrome 1 62 0.083
76
LSC001 Lesch-Nyhan Syndrome 62 0.083
77
TXC005 Toxic Shock Syndrome 62 0.083
78
NTR005 Nutritional Deficiency Disease 62 0.083
79
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.083
80
FTT001 Fatty Liver Disease 61 0.083
81
YLL002 Yellow Fever 61 0.083
82
HPT019 Hepatic Encephalopathy 60 0.083
83
ACN002 Acanthosis Nigricans 60 0.083
84
P AXN002 Axenfeld-Rieger Syndrome 59 0.083
85
P ALC033 Alcohol Use Disorder 58 0.083
86
LYM027 Lymphopenia 58 0.083
87
IRN002 Iron Metabolism Disease 57 0.083
88
P EXN002 Exanthem 57 0.083
89
CHK001 Chikungunya 57 0.083
90
THR024 Thrombosis 57 0.083
91
P END033 Endocarditis 57 0.083
92
P CRD246 Cardiovascular System Disease 57 0.083
93
PHR003 Pharyngitis 57 0.083
94
P MYS005 Myositis 56 0.083
95
P CHN012 Chondrosarcoma 56 0.083
96
c ACT134 Acute Liver Failure 56 0.083
97
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.083
98
P NRP001 Neuropathy 56 0.083
99
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.083
100
CRY003 Cryptosporidiosis 54 0.083
101
THR013 Thoracic Outlet Syndrome 54 0.083
102
P ART021 Arteriosclerosis 54 0.083
103
P TRM003 Tremor 54 0.083
104
NNL006 Non-Alcoholic Steatohepatitis 54 0.083
105
PNC001 Pancytopenia 54 0.083
106
TRC003 Trichomoniasis 53 0.083
107
c MCR113 Microvascular Complications of Diabetes 3 52 0.083
108
P CNG436 Congenital Disorder of Deglycosylation 52 0.083
109
PTH003 Pathologic Nystagmus 52 0.083
110
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.083
111
TLN003 Telangiectasis 52 0.083
112
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.083
113
CLR109 Colorectal Adenocarcinoma 51 0.083
114
MGL001 Megaloblastic Anemia 51 0.083
115
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.083
116
P MTR003 Mitral Valve Stenosis 50 0.083
117
IMP004 Impetigo 49 0.083
118
URM002 Uremia 49 0.083
119
c MCR120 Microvascular Complications of Diabetes 7 47 0.083
120
ADR040 Adrenal Gland Pheochromocytoma 46 0.083
121
GLL048 Glial Tumor 45 0.083
122
HPT004 Hepatic Coma 45 0.083
123
NWC001 Newcastle Disease 45 0.083
124
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.083
125
HPT082 Hepatic Adenomas, Familial 44 0.083
126
HMP009 Haemophilus Influenzae 43 0.083
127
MST004 Mast Cell Neoplasm 42 0.083
128
c MCR130 Microvascular Complications of Diabetes 6 41 0.083
129
c MCR133 Microvascular Complications of Diabetes 4 41 0.083
130
GLY015 Glycine N-Methyltransferase Deficiency 39 0.083
131
AMN002 Amino Acid Metabolic Disorder 39 0.083
132
CHL045 Choline Deficiency Disease 39 0.083
133
c PRG020 Paragangliomas 3 39 0.083
134
ADP007 Adie Pupil 39 0.083
135
EXT007 Extracutaneous Mastocytoma 38 0.083
136
STR077 Streptococcal Toxic-Shock Syndrome 37 0.083
137
ATX010 Ataxia Neuropathy Spectrum 34 0.083
138
CKS001 Ck Syndrome 33 0.083
139
ALR002 Al-Raqad Syndrome 33 0.083
140
ACT064 Acute Necrotizing Encephalitis 33 0.083
141
MYC088 Mycobacterium Avium Complex Infections 29 0.083
142
HNM002 Hinman Syndrome 27 0.083
143
AND005 Androgen Insensitivity Syndrome, Mild 19 0.083
144
BLD137 Blood Group--Ahonen 16 0.083
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