Search results for Coproporphyrin I

64 hits were found for Coproporphyrin I

# Family MCID Name MIFTS Score
1
P PRP029 Porphyria 58 0.260
2
P LKM002 Leukemia 69 0.258
3
P LYM118 Lymphoma 70 0.244
4
LYM019 Lymphosarcoma 48 0.213
5
P LYM031 Lymphocytic Leukemia 56 0.197
6
DBN001 Dubin-Johnson Syndrome 58 0.188
7
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.175
8
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.172
9
P LVR013 Liver Disease 71 0.166
10
P MYC007 Myocardial Infarction 74 0.160
11
P LKM062 Leukemia, Acute Lymphoblastic 68 0.158
12
LVR012 Liver Cirrhosis 67 0.155
13
P HPT023 Hepatocellular Carcinoma 99 0.154
14
CYT002 Cytokine Deficiency 46 0.148
15
ATX019 Ataxia with Vitamin E Deficiency 46 0.145
16
c ACT073 Acute Leukemia 59 0.144
17
CPR004 Coproporphyria, Hereditary 57 0.143
18
BLR008 Bilirubin Metabolic Disorder 58 0.140
19
DFC004 Deficiency Anemia 77 0.139
20
LYM040 Lymphoblastic Lymphoma 54 0.139
21
DPR016 Depression 64 0.135
22
c ACT075 Acute Myocardial Infarction 59 0.133
23
P PRP003 Porphyria Cutanea Tarda 66 0.133
24
P NRF023 Neurofibromatosis, Type Ii 77 0.131
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.131
26
P HPT021 Hepatitis 69 0.128
27
BRK010 Burkitt Lymphoma 68 0.128
28
c HPT073 Hepatitis C Virus 74 0.125
29
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.123
30
PRP083 Porphyria, Acute Intermittent 62 0.123
31
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.122
32
PLM033 Pulmonary Embolism 60 0.116
33
HYP236 Hyperbilirubinemia, Rotor Type 46 0.114
34
PRP082 Porphyria, Congenital Erythropoietic 55 0.114
35
CHL068 Cholestasis 61 0.113
36
ATS010 Autosomal Recessive Disease 49 0.113
37
P MSC005 Muscular Dystrophy 68 0.112
38
SKN016 Skin Disease 64 0.112
39
c ACT078 Acute Porphyria 49 0.111
40
c CNT033 Central Nervous System Cancer 51 0.111
41
P NRV006 Nervous System Cancer 55 0.111
42
VRG001 Variegate Porphyria 55 0.106
43
PFF001 Pfeiffer Syndrome 79 0.104
44
SLC006 Silicosis 55 0.102
45
c VRL010 Viral Hepatitis 56 0.101
46
c ACT068 Acute Cystitis 63 0.095
47
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.093
48
PRN011 Pernicious Anemia 51 0.079
49
BLR001 Biliary Atresia 51 0.075
50
P PRP056 Porphyria, Acute Hepatic 46 0.074
51
HYP781 Hypoascorbemia 48 0.072
52
GLB001 Gilbert Syndrome 58 0.068
53
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.068
54
KWS001 Kwashiorkor 46 0.068
55
P MGL001 Megaloblastic Anemia 54 0.066
56
c PRT132 Protoporphyria, Erythropoietic, 1 59 0.061
57
NNT012 Neonatal Jaundice 48 0.060
58
ERY010 Erythrasma 23 0.057
59
P ALG028 Alagille Syndrome 1 70 0.056
60
HYP171 Hyperphenylalaninemia Due to Dehydratase Deficiency 16 0.053
61
MCN007 Meconium Aspiration Syndrome 53 0.051
62
c FML324 Familial Porphyria Cutanea Tarda 31 0.051
63
c CHR471 Chronic Hepatic Porphyria 16 0.051
64
AMN017 Aminolevulinic Acid Dehydratase Deficiency Porphyria 7 0.051
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