Search results for "[genes] CAT"

57 hits were found for '[genes] CAT'

# Family MCID Name MIFTS Score
1
ACT209 Acatalasemia 35 21.626
2
P ALZ034 Alzheimer Disease 98 13.678
3
ADR007 Adrenoleukodystrophy 76 13.678
4
WLS001 Wilson Disease 74 13.678
5
P RFS001 Refsum Disease 65 13.678
6
CHR012 Chronic Granulomatous Disease 60 13.678
7
c PRX045 Peroxisome Biogenesis Disorder 1b 50 13.678
8
P PNM006 Pneumoconiosis 45 13.678
9
DBT008 Diabetic Angiopathy 38 13.678
10
c SYS001 Systemic Lupus Erythematosus 90 11.845
11
P RHM011 Rheumatoid Arthritis 88 11.845
12
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 11.845
13
P AST005 Asthma 77 11.845
14
ANR002 Aniridia 72 11.845
15
ACN011 Acne 55 11.845
16
VSC007 Vascular Disease 55 11.845
17
PRT103 Protoporphyria, Erythropoietic, Autosomal Recessive 48 11.845
18
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 48 11.845
19
P ALC004 Alcohol Abuse 47 11.845
20
ISC004 Ischemia 47 11.845
21
GLC085 Glucose-6-Phosphate Dehydrogenase Deficiency 46 11.845
22
BRS051 Breast Disease 44 11.845
23
NNT017 Neonatal Adrenoleukodystrophy 42 11.845
24
MCR018 Microcytic Anemia 39 11.845
25
ASB001 Asbestosis 39 11.845
26
PTY002 Pityriasis Versicolor 36 11.845
27
DBT007 Diabetic Cataract 28 11.845
28
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 9.672
29
c PRK057 Parkinson Disease, Late-Onset 73 9.672
30
PST028 Post-Traumatic Stress Disorder 53 9.672
31
P AVS004 Avascular Necrosis of the Femoral Head 49 9.672
32
MRR001 Merrf Syndrome 48 9.672
33
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 48 9.672
34
c CNG124 Congenital Rubella 47 9.672
35
CRY003 Cryptosporidiosis 45 9.672
36
ASP003 Aseptic Meningitis 44 9.672
37
P HYP141 Hyperphenylalaninemia 44 9.672
38
HYP107 Hyperornithinemia-Hyperammonemia-Homocitrullinemia Syndrome 43 9.672
39
HMS001 Hemosiderosis 40 9.672
40
RTN003 Retinal Ischemia 40 9.672
41
MYL013 Myeloperoxidase Deficiency 40 9.672
42
SCL003 Social Phobia 38 9.672
43
HYP003 Hypermethioninemia 38 9.672
44
c HMG001 Hemoglobin C Disease 36 9.672
45
SPR016 Spermatic Cord Torsion 34 9.672
46
FVS001 Favism 33 9.672
47
PRX034 Peroxisome Disorders 32 9.672
48
PHT002 Photokeratitis 28 9.672
49
CSP003 Cisplatin Toxicity 27 9.672
50
URG001 Urogenital Tuberculosis 27 9.672
51
SLF001 Sulfhemoglobinemia 25 9.672
52
MNN024 Meningitis and Encephalitis 23 9.672
53
VTR002 Vitreous Syneresis 21 9.672
54
DBT081 Diabetic Encephalopathy 21 9.672
55
MGK002 Megakaryocytic Tumor 20 9.672
56
TTR001 Tetralogy of Fallot 68 6.839
57
TXC002 Toxic Encephalopathy 43 6.839