Search results for Uroporphyrinogen I

52 hits were found for Uroporphyrinogen I

# Family MCID Name MIFTS Score
1
P PRP029 Porphyria 62 0.760
2
P PRP003 Porphyria Cutanea Tarda 67 0.533
3
PRP082 Porphyria, Congenital Erythropoietic 55 0.382
4
PRP083 Porphyria, Acute Intermittent 63 0.348
5
c FML324 Familial Porphyria Cutanea Tarda 30 0.299
6
c PRP091 Porphyria Cutanea Tarda, Type I 30 0.222
7
ATS010 Autosomal Recessive Disease 48 0.215
8
c HPT001 Hepatitis C 63 0.186
9
c HMC039 Hemochromatosis, Type 1 74 0.181
10
48X005 48,xyyy 39 0.180
11
HLX001 Helix Syndrome 47 0.178
12
P NRP001 Neuropathy 56 0.170
13
MYL009 Myelodysplastic Syndrome 70 0.159
14
P KDN018 Kidney Disease 70 0.158
15
P RRH023 Rare Hereditary Hemochromatosis 41 0.158
16
HMS001 Hemosiderosis 54 0.157
17
c ACT078 Acute Porphyria 49 0.150
18
P LVR013 Liver Disease 68 0.149
19
VRL011 Viral Infectious Disease 61 0.144
20
CTN011 Cutaneous Porphyria 38 0.143
21
47X002 47,xyy 49 0.138
22
P PRP019 Peripheral Nervous System Disease 57 0.138
23
c CHR471 Chronic Hepatic Porphyria 16 0.136
24
P HML002 Hemolytic Anemia 62 0.135
25
BLR008 Bilirubin Metabolic Disorder 57 0.129
26
c HPT073 Hepatitis C Virus 70 0.127
27
IRN002 Iron Metabolism Disease 57 0.125
28
END030 End Stage Renal Failure 58 0.124
29
VRG001 Variegate Porphyria 56 0.124
30
ERY051 Erythroleukemia, Familial 56 0.120
31
c CHR684 Chronic Kidney Disease 66 0.119
32
P HYP077 Hypertrichosis 50 0.115
33
SKN016 Skin Disease 63 0.115
34
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.114
35
c INH020 Inherited Metabolic Disorder 46 0.114
36
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.106
37
c VRL010 Viral Hepatitis 51 0.104
38
P ALC033 Alcohol Use Disorder 58 0.104
39
CHR178 Chromosomal Triplication 35 0.102
40
P SDR002 Siderosis 44 0.102
41
FTT001 Fatty Liver Disease 61 0.097
42
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.087
43
CPR004 Coproporphyria, Hereditary 57 0.082
44
P OBS001 Obstructive Jaundice 48 0.079
45
ADR016 Adrenal Cortical Carcinoma 48 0.078
46
c DWL002 Dowling-Degos Disease 1 58 0.078
47
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.078
48
ADR004 Adrenal Cortical Adenocarcinoma 38 0.077
49
P HMC002 Homocystinuria 54 0.070
50
DBN001 Dubin-Johnson Syndrome 59 0.064
51
CHR186 Chromosome 11p Duplication 10 0.054
52
DST081 Distal Trisomy 11q 9 0.054
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