Search results for Glucose 6-phosphate

182 hits were found for Glucose 6-phosphate

# Family MCID Name MIFTS Score
1
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 5.365
2
HYP056 Hypoglycemia 66 0.683
3
HYP066 Hyperglycemia 61 0.674
4
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.451
5
P HML002 Hemolytic Anemia 63 0.240
6
P GLY013 Glycogen Storage Disease 60 0.217
7
48X005 48,xyyy 39 0.204
8
P LVR013 Liver Disease 68 0.196
9
LVR012 Liver Cirrhosis 62 0.194
10
INS024 Insulin-Like Growth Factor I 79 0.193
11
P ALZ034 Alzheimer Disease 88 0.169
12
ACR007 Acromegaly 71 0.169
13
CYS001 Cystic Fibrosis 81 0.168
14
PRT037 Pertussis 65 0.163
15
c CHR684 Chronic Kidney Disease 70 0.161
16
P BRS047 Breast Cancer 97 0.161
17
P HPT023 Hepatocellular Carcinoma 100 0.161
18
P CTR002 Cataract 60 0.158
19
END086 End Stage Renal Disease 51 0.152
20
ANX004 Anoxia 40 0.152
21
P HRT032 Heart Disease 75 0.148
22
CHL014 Cholera 59 0.147
23
P HYP076 Hyperthyroidism 55 0.143
24
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.140
25
CNG034 Congestive Heart Failure 69 0.140
26
P NRB001 Neuroblastoma 72 0.133
27
NNT012 Neonatal Jaundice 53 0.132
28
P CLR023 Colorectal Cancer 99 0.132
29
MLR004 Malaria 81 0.131
30
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.131
31
47X002 47,xyy 49 0.128
32
P ADN016 Adenocarcinoma 64 0.126
33
P THL005 Thalassemia 60 0.125
34
P OVR082 Overgrowth Syndrome 50 0.124
35
BLR008 Bilirubin Metabolic Disorder 57 0.124
36
P NTR004 Neutropenia 63 0.123
37
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.123
38
CRB004 Cerebral Artery Occlusion 45 0.121
39
DFC004 Deficiency Anemia 70 0.119
40
HLX001 Helix Syndrome 47 0.117
41
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.117
42
P MYP004 Myopathy 70 0.115
43
BNR002 Bone Resorption Disease 48 0.114
44
P HRP006 Herpes Simplex 65 0.114
45
CYT002 Cytokine Deficiency 42 0.114
46
RNL077 Renal Fibrosis 47 0.112
47
PPL052 Papillomatosis, Confluent and Reticulated 33 0.111
48
P ENC018 Encephalopathy 61 0.111
49
LYS002 Lysosomal Storage Disease 52 0.110
50
ADN018 Adenoma 59 0.110
51
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.110
52
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 38 0.109
53
P PRS040 Prostate Cancer 97 0.109
54
CLN015 Colon Adenocarcinoma 65 0.107
55
P MCL001 Mucolipidosis 48 0.103
56
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.103
57
CHR074 Choriocarcinoma 47 0.102
58
HYP043 Hyperandrogenism 48 0.100
59
c GLY060 Glycogen Storage Disease Ia 63 0.098
60
SQM006 Squamous Cell Carcinoma 60 0.097
61
c GLY016 Glycogen Storage Disease Ib 40 0.096
62
SVR004 Severe Combined Immunodeficiency 73 0.096
63
P LNG064 Lung Cancer Susceptibility 3 78 0.096
64
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 26 0.095
65
HMS001 Hemosiderosis 54 0.093
66
P RRH023 Rare Hereditary Hemochromatosis 41 0.093
67
c GLY008 Glycogen Storage Disease Ii 70 0.092
68
c FML035 Familial Hyperlipidemia 55 0.090
69
CRV035 Cervical Cancer 76 0.086
70
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.084
71
STM007 Stomatitis 50 0.084
72
c PCH010 Pachyonychia Congenita 3 44 0.083
73
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.082
74
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.082
75
P LTR001 Lateral Sclerosis 54 0.082
76
OST012 Osteoarthritis 78 0.082
77
P HPT021 Hepatitis 67 0.082
78
IRN002 Iron Metabolism Disease 57 0.082
79
P RHB003 Rhabdomyosarcoma 63 0.081
80
P AST007 Astrocytoma 51 0.081
81
P BLD134 Bladder Cancer 79 0.080
82
P MSC005 Muscular Dystrophy 66 0.080
83
MSC007 Muscle Hypertrophy 64 0.080
84
PLY150 Polykaryocytosis Inducer 31 0.079
85
BCT022 Bacterial Infectious Disease 56 0.079
86
P MSC003 Muscular Atrophy 52 0.079
87
P LKM002 Leukemia 68 0.078
88
c VRL010 Viral Hepatitis 52 0.078
89
HRW001 Hair Whorl 36 0.078
90
ATS010 Autosomal Recessive Disease 48 0.077
91
P MYT002 Myotonic Dystrophy 49 0.076
92
P SCK005 Sickle Cell Disease 50 0.076
93
CHC001 Chickenpox 60 0.075
94
c HMC039 Hemochromatosis, Type 1 74 0.074
95
c HPT016 Hepatitis B 59 0.074
96
HMP009 Haemophilus Influenzae 43 0.074
97
SLP001 Sleeping Sickness 54 0.073
98
CNG017 Congenital Nonspherocytic Hemolytic Anemia 35 0.073
99
P RHM011 Rheumatoid Arthritis 80 0.073
100
P MYL006 Myeloid Leukemia 60 0.073
101
c GLY017 Glycogen Storage Disease Ic 30 0.072
102
P INF037 Inflammatory Bowel Disease 54 0.071
103
TLN003 Telangiectasis 52 0.071
104
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 26 0.071
105
c NRF023 Neurofibromatosis, Type Ii 80 0.070
106
CHG001 Chagas Disease 66 0.070
107
MNN042 Meningioma, Radiation-Induced 62 0.069
108
P ATX030 Ataxia-Telangiectasia 82 0.068
109
c MNN043 Meningioma, Familial 74 0.068
110
P PLM036 Pulmonary Fibrosis 65 0.067
111
ERY051 Erythroleukemia, Familial 56 0.067
112
P KRN004 Kernicterus 47 0.067
113
P KDN017 Kidney Cancer 60 0.067
114
SPN021 Spinal Meningioma 50 0.067
115
SCR001 Secretory Meningioma 41 0.067
116
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.067
117
c BRN108 Branchiootic Syndrome 1 62 0.066
118
PLS011 Plasmacytoma 56 0.066
119
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.065
120
P TRC086 Trichohepatoenteric Syndrome 1 62 0.064
121
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.063
122
P NMN002 Niemann-Pick Disease 59 0.063
123
CHL123 Chlamydia 59 0.063
124
P CHN012 Chondrosarcoma 56 0.062
125
c GLC079 Glaucoma 1, Open Angle, P 23 0.062
126
c WLM018 Wilms Tumor 5 61 0.061
127
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.061
128
DWR001 Dwarfism 44 0.061
129
c HPT007 Hepatitis E 53 0.060
130
P MTR014 Motor Neuron Disease 65 0.059
131
P INS002 in Situ Carcinoma 53 0.057
132
SPL018 Splenomegaly 48 0.057
133
GLM044 Glomerular Disease 37 0.057
134
c PRG106 Progressive Muscular Dystrophy 33 0.057
135
SCK003 Sickle Cell Anemia 74 0.056
136
VRL011 Viral Infectious Disease 61 0.054
137
IRN001 Iron Deficiency Anemia 59 0.054
138
PHS025 Phosphatase, Acid, of Tissues 28 0.053
139
P SPN046 Spinal Muscular Atrophy 62 0.053
140
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.053
141
P HRD011 Hereditary Spherocytosis 60 0.053
142
TRY001 Trypanosomiasis 50 0.053
143
P MTC133 Mitochondrial Myopathy 49 0.053
144
FRC001 Fructose-1,6-Bisphosphatase Deficiency 49 0.053
145
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.053
146
ARG004 Argyria 27 0.053
147
P SYS005 Systemic Scleroderma 68 0.051
148
P CHR012 Chronic Granulomatous Disease 67 0.051
149
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.051
150
P GCH001 Gaucher's Disease 63 0.051
151
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.051
152
P MTH007 Methemoglobinemia 46 0.051
153
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.051
154
MYL009 Myelodysplastic Syndrome 70 0.049
155
NRM005 Neuromuscular Disease 64 0.049
156
P SLM003 Salmonellosis 55 0.049
157
c GCH015 Gaucher Disease, Type I 70 0.046
158
END041 Endometrial Adenocarcinoma 63 0.046
159
BRS099 Breast Ductal Carcinoma 62 0.046
160
P LKD001 Leukodystrophy 59 0.046
161
DCT002 Ductal Carcinoma in Situ 59 0.046
162
P PLY041 Polymyositis 57 0.046
163
PLS006 Plasmodium Vivax Malaria 51 0.046
164
P BRS053 Breast Fibroadenoma 49 0.046
165
THY006 Thymus Lymphoma 26 0.046
166
FBR012 Fabry Disease 72 0.044
167
P ASP006 Aspergillosis 69 0.044
168
c NMN015 Niemann-Pick Disease, Type C1 68 0.044
169
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.044
170
CRV040 Cervix Carcinoma 51 0.044
171
HMG002 Hemoglobinuria 50 0.044
172
RBF001 Riboflavin Deficiency 49 0.044
173
CHL147 Chlamydia Pneumonia 48 0.044
174
P MTC003 Metachromatic Leukodystrophy 70 0.040
175
MYL005 Myelofibrosis 70 0.040
177
GLB001 Gilbert Syndrome 58 0.040
178
P HRD012 Hereditary Elliptocytosis 51 0.040
179
MCR019 Microglandular Adenosis 43 0.040
180
c ELL005 Elliptocytosis 2 38 0.040
181
c ELL006 Elliptocytosis 3 36 0.040
182
CRT020 Cortisone Reductase Deficiency 31 0.040
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