Search results for Porphobilinogen

58 hits were found for Porphobilinogen

# Family MCID Name MIFTS Score
1
PRP083 Porphyria, Acute Intermittent 64 6.866
2
P PRP056 Porphyria, Acute Hepatic 48 6.386
3
P PRP029 Porphyria 62 0.885
4
c ACT078 Acute Porphyria 51 0.376
5
VRG001 Variegate Porphyria 56 0.183
6
P PRP003 Porphyria Cutanea Tarda 67 0.171
7
P LKM002 Leukemia 68 0.129
8
ERY051 Erythroleukemia, Familial 56 0.129
9
P SCH015 Schizophrenia 74 0.112
10
IRN002 Iron Metabolism Disease 57 0.112
11
CTN011 Cutaneous Porphyria 38 0.112
12
DFC004 Deficiency Anemia 70 0.091
13
P LVR013 Liver Disease 68 0.091
14
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.091
15
P GLM045 Glioma 63 0.091
16
LVR012 Liver Cirrhosis 62 0.091
17
P ENC018 Encephalopathy 61 0.091
18
CPR004 Coproporphyria, Hereditary 57 0.091
19
P NRP001 Neuropathy 56 0.091
20
PRP082 Porphyria, Congenital Erythropoietic 56 0.091
21
47X002 47,xyy 49 0.091
22
GLL048 Glial Tumor 45 0.091
23
48X005 48,xyyy 39 0.091
24
P HPT023 Hepatocellular Carcinoma 100 0.065
25
P LKM071 Leukemia, Chronic Lymphocytic 79 0.065
26
SCK003 Sickle Cell Anemia 74 0.065
27
P MLT020 Multiple Sclerosis 72 0.065
28
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.065
29
PLM031 Poliomyelitis 64 0.065
30
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.065
31
P THL005 Thalassemia 60 0.065
32
DBN001 Dubin-Johnson Syndrome 59 0.065
33
P BRS044 Breast Adenocarcinoma 59 0.065
34
IRN001 Iron Deficiency Anemia 59 0.065
35
P GLL022 Guillain-Barre Syndrome 59 0.065
36
c ACT073 Acute Leukemia 58 0.065
37
P TYR004 Tyrosinemia 58 0.065
38
CNS004 Constipation 58 0.065
39
P PRP019 Peripheral Nervous System Disease 58 0.065
40
P PLY019 Polyneuropathy 56 0.065
41
PRN011 Pernicious Anemia 53 0.065
42
SCH012 Schizoaffective Disorder 50 0.065
43
URM002 Uremia 49 0.065
44
SPL018 Splenomegaly 48 0.065
45
P MRC003 Mercury Poisoning 48 0.065
46
HLX001 Helix Syndrome 47 0.065
47
c INH020 Inherited Metabolic Disorder 47 0.065
48
LYM019 Lymphosarcoma 46 0.065
49
P BNG032 Benign Mesothelioma 46 0.065
50
P SPR119 Spermatogenic Failure, X-Linked, 1 39 0.065
51
P DYS021 Dysautonomia 39 0.065
52
P AXN001 Axonal Neuropathy 36 0.065
53
CHR178 Chromosomal Triplication 35 0.065
54
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.065
55
c FML324 Familial Porphyria Cutanea Tarda 31 0.065
56
ARG004 Argyria 27 0.065
57
CHS007 Chester Porphyria 15 0.065
58
ANM041 Anemia, Nonspherocytic Hemolytic, Possibly Due to Defect in Porphyrin Metabolism 8 0.065
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