Search results for Dihydroxyacetone phosphate

49 hits were found for Dihydroxyacetone phosphate

# Family MCID Name MIFTS Score
1
RCK004 Rickets 70 0.214
2
P ZLL001 Zellweger Syndrome 56 0.162
3
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.155
4
P HML002 Hemolytic Anemia 64 0.137
5
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.133
6
P DBT009 Diabetes Mellitus 66 0.127
7
48X005 48,xyyy 37 0.125
8
DRM006 Dermatitis 63 0.124
9
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.118
10
P CHN044 Chondrodysplasia Punctata Syndrome 42 0.115
11
PRX001 Peroxisomal Disease 45 0.113
12
TRS021 Triosephosphate Isomerase Deficiency 44 0.113
13
47X002 47,xyy 49 0.104
14
FTT001 Fatty Liver Disease 63 0.102
15
P RHZ001 Rhizomelic Chondrodysplasia Punctata 53 0.101
16
P SKN015 Skin Carcinoma 67 0.100
17
P LVR013 Liver Disease 71 0.100
18
CNT047 Contact Dermatitis 58 0.099
19
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.096
20
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.096
21
LVR012 Liver Cirrhosis 67 0.094
22
ADR007 Adrenoleukodystrophy 72 0.093
23
AGN016 Aging 58 0.092
24
P PSR002 Psoriasis 63 0.091
25
PST011 Pustulosis of Palm and Sole 51 0.090
26
ATS010 Autosomal Recessive Disease 49 0.090
27
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.090
28
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.085
29
ADR022 Adrenomyeloneuropathy 39 0.084
30
VRL011 Viral Infectious Disease 62 0.082
31
P GLY013 Glycogen Storage Disease 59 0.079
32
c CNG027 Congenital Hemolytic Anemia 48 0.073
33
P PRP029 Porphyria 58 0.072
34
ALL010 Allergic Contact Dermatitis 56 0.072
35
P URT039 Urticaria 61 0.068
36
c GRV008 Graves Disease 1 55 0.068
37
FRC011 Fructose Intolerance, Hereditary 52 0.067
38
CRD137 Cardiogenic Shock 50 0.064
39
URT049 Urate Oxidase, Pseudogene 26 0.064
40
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.059
41
HPT014 Hepatorenal Syndrome 49 0.059
42
CYN003 Cyanide Poisoning 24 0.059
43
c PRX059 Peroxisome Biogenesis Disorder 1a 57 0.056
44
P ICH004 Ichthyosis 55 0.056
45
P HYP083 Hypopituitarism 53 0.056
46
ICH054 Ichthyosis, X-Linked 52 0.056
47
P CHN074 Chondrodysplasia Punctata 2, X-Linked Dominant 48 0.056
48
IRR003 Irritant Dermatitis 46 0.056
49
NNT017 Neonatal Adrenoleukodystrophy 46 0.056
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