Search results for Dihydroxyacetone phosphate

50 hits were found for Dihydroxyacetone phosphate

# Family MCID Name MIFTS Score
1
RCK004 Rickets 68 0.219
2
P ZLL001 Zellweger Syndrome 57 0.159
3
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.153
4
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.147
5
P HML002 Hemolytic Anemia 63 0.134
6
DRM006 Dermatitis 61 0.124
7
P DBT009 Diabetes Mellitus 64 0.123
8
MTB004 Metabolic Acidosis 50 0.122
9
48X005 48,xyyy 39 0.121
10
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.114
11
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.114
12
PRX001 Peroxisomal Disease 46 0.112
13
TRS021 Triosephosphate Isomerase Deficiency 44 0.111
14
FTT001 Fatty Liver Disease 61 0.102
15
P RHZ001 Rhizomelic Chondrodysplasia Punctata 53 0.099
16
P SKN015 Skin Carcinoma 66 0.099
17
CNT047 Contact Dermatitis 58 0.098
18
P LVR013 Liver Disease 68 0.096
19
47X002 47,xyy 49 0.096
20
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.095
21
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.095
22
LVR012 Liver Cirrhosis 62 0.092
23
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.092
24
ADR007 Adrenoleukodystrophy 75 0.091
25
ATS010 Autosomal Recessive Disease 48 0.089
26
P PSR002 Psoriasis 62 0.088
27
PST011 Pustulosis of Palm and Sole 52 0.088
28
AGN016 Aging 56 0.085
29
ADR022 Adrenomyeloneuropathy 38 0.083
30
VRL011 Viral Infectious Disease 61 0.081
31
P GLY013 Glycogen Storage Disease 60 0.078
32
c CNG027 Congenital Hemolytic Anemia 50 0.072
33
ALL010 Allergic Contact Dermatitis 56 0.071
34
P PRP029 Porphyria 62 0.069
35
c GRV008 Graves Disease 1 56 0.067
36
FRC011 Fructose Intolerance, Hereditary 57 0.065
37
P URT039 Urticaria 58 0.063
38
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.063
39
CRD137 Cardiogenic Shock 47 0.063
40
URT049 Urate Oxidase, Pseudogene 25 0.063
41
CYN003 Cyanide Poisoning 24 0.061
42
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.058
43
HPT014 Hepatorenal Syndrome 50 0.058
44
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.055
45
P ICH004 Ichthyosis 54 0.055
46
ICH054 Ichthyosis, X-Linked 53 0.055
47
P HYP083 Hypopituitarism 53 0.055
48
IRR003 Irritant Dermatitis 49 0.055
49
P CHN074 Chondrodysplasia Punctata 2, X-Linked Dominant 49 0.055
50
NNT017 Neonatal Adrenoleukodystrophy 47 0.055
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