Search results for "[genes] ALB"

103 hits were found for '[genes] ALB'

# Family MCID Name MIFTS Score
1
DYS070 Dysalbuminemic Hyperthyroxinemia 27 15.188
2
LVR012 Liver Cirrhosis 66 12.401
3
PRT036 Peritonitis 61 12.401
4
OVR029 Ovarian Hyperstimulation Syndrome 60 12.401
5
P NPH012 Nephrotic Syndrome 60 12.401
6
P GLM007 Glomerulonephritis 59 12.401
7
VSC007 Vascular Disease 59 12.401
8
HPT014 Hepatorenal Syndrome 48 12.401
9
PRT019 Protein-Losing Enteropathy 47 12.401
10
P KRN004 Kernicterus 46 12.401
11
PRT039 Proteinuria 43 12.401
12
GLM011 Glomerulosclerosis 40 12.401
13
MRS001 Marasmus 40 12.401
14
HPT009 Hepatopulmonary Syndrome 38 12.401
15
HYP029 Hyperthyroxinemia 36 12.401
16
P ANL018 Analbuminemia 19 10.740
17
c CNG336 Congenital Analbuminemia 11 10.740
18
TBR010 Tuberculosis 73 8.769
19
P LVR013 Liver Disease 62 8.769
20
c HPT016 Hepatitis B 60 8.769
21
c MTB001 Metabolic Syndrome X 58 8.769
22
STR008 Strongyloidiasis 58 8.769
23
P GLL020 Gallbladder Disease 56 8.769
24
CMM005 Common Cold 54 8.769
25
P HYP620 Hypoprothrombinemia 54 8.769
26
EXT034 Extrinsic Allergic Alveolitis 54 8.769
27
HYD012 Hydrops Fetalis 53 8.769
28
ART005 Arteriovenous Malformation 53 8.769
29
INT051 Intussusception 53 8.769
30
P INT070 Intestinal Obstruction 53 8.769
31
P DYS026 Dysfibrinogenemia 52 8.769
32
ACR003 Acrodermatitis Enteropathica 52 8.769
33
P RNV001 Renovascular Hypertension 52 8.769
34
BRN002 Bronchiolitis 52 8.769
35
CNG048 Congenital Hepatic Fibrosis 51 8.769
36
SCR002 Scurvy 51 8.769
37
c SCN045 Secondary Amyloidosis 50 8.769
38
BCT004 Bacteriuria 50 8.769
39
MLR002 Miliary Tuberculosis 50 8.769
40
c ACT071 Acute Kidney Failure 50 8.769
41
HYP063 Hypersplenism 50 8.769
42
PRC012 Pericardial Effusion 49 8.769
43
ANR004 Anuria 48 8.769
44
BLS002 Blastomycosis 48 8.769
45
P CMP008 Compartment Syndrome 47 8.769
46
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 47 8.769
47
CLC001 Calciphylaxis 47 8.769
48
ACR005 Acrodermatitis 47 8.769
49
LPP002 Lipoprotein Glomerulopathy 46 8.769
50
PLY020 Polyradiculoneuropathy 46 8.769
51
PRR002 Pure Red-Cell Aplasia 46 8.769
52
P PLL002 Pellagra 45 8.769
53
GST045 Gastroenteritis 45 8.769
54
P CPL003 Capillary Leak Syndrome 45 8.769
55
DYS073 Dysphagia 45 8.769
56
YLL001 Yellow Nail Syndrome 45 8.769
57
NM001 Noma 44 8.769
58
ESN005 Eosinophilic Gastroenteritis 44 8.769
59
ADR021 Adrenocorticotropic Hormone Deficiency 44 8.769
60
P BRY001 Berylliosis 43 8.769
61
P PYL005 Pyelonephritis 43 8.769
62
LPD004 Lipoid Nephrosis 43 8.769
63
VSC044 Visceral Myopathy 43 8.769
64
CRN014 Cronkhite-Canada Syndrome 43 8.769
65
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 43 8.769
66
RNL015 Renal Hypertension 42 8.769
67
DRG002 Drug-Induced Hepatitis 42 8.769
68
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 41 8.769
69
ACT040 Acute Poststreptococcal Glomerulonephritis 41 8.769
70
PST010 Pasteurellosis 41 8.769
71
KWS001 Kwashiorkor 41 8.769
72
CHY006 Chylous Ascites 40 8.769
73
NNT024 Neonatal Stroke 40 8.769
74
c CNG415 Congenital Disorder of Glycosylation, Type Ia 40 8.769
75
ACT167 Acute Generalized Exanthematous Pustulosis 40 8.769
76
CNS002 Constrictive Pericarditis 40 8.769
77
c CHR098 Chronic Pyelonephritis 40 8.769
78
ABD004 Abdominal Tuberculosis 39 8.769
79
c VRL005 Viral Pneumonia 39 8.769
80
ETH004 Euthyroid Sick Syndrome 39 8.769
81
CHN005 Choanal Atresia 39 8.769
82
HPT008 Hepatic Tuberculosis 39 8.769
83
PLM052 Pulmonary Arteriovenous Malformation 39 8.769
84
ANL022 Anal Fistula 39 8.769
85
CHL039 Choledocholithiasis 39 8.769
86
HYP114 Hypertensive Nephropathy 38 8.769
87
c ACT004 Acute Diarrhea 37 8.769
88
SRF006 Surfactant Dysfunction 36 8.769
89
HYP008 Hypertensive Retinopathy 36 8.769
90
ESP002 Esophageal Varix 35 8.769
91
TRC062 Tricuspid Atresia 33 8.769
92
ENT007 Enteropathica 32 8.769
93
c SYS007 Systemic Capillary Leak Syndrome 32 8.769
94
LYM024 Lymphatic System Disease 31 8.769
95
NNM005 Non-Immune Hydrops Fetalis 30 8.769
96
IMM039 Immune Hydrops Fetalis 29 8.769
97
P FML187 Familial Hypertension 29 8.769
98
DCB001 Decubitus Ulcer 29 8.769
99
CPP003 Cap Polyposis 22 8.769
100
HYP281 Hypoproteinemia, Hypercatabolic 22 8.769
101
IMM053 Immunotactoid Glomerulopathy 21 8.769
102
PPT002 Peptic Ulcer Perforation 18 8.769
103
c HYP072 Hypersensitivity Reaction Type Iii Disease 16 8.769