Search results for "[genes] CAT"

62 hits were found for '[genes] CAT'

# Family MCID Name MIFTS Score
1
ACT209 Acatalasemia 36 20.281
2
P ALZ034 Alzheimer Disease 93 13.521
3
WLS001 Wilson Disease 73 13.521
4
ADR007 Adrenoleukodystrophy 71 13.521
5
CHR012 Chronic Granulomatous Disease 69 13.521
6
P RFS001 Refsum Disease 60 13.521
7
P PRP023 Peripheral Neuropathy 56 13.521
8
P PNM006 Pneumoconiosis 55 13.521
9
P RHM011 Rheumatoid Arthritis 90 11.709
10
c SYS001 Systemic Lupus Erythematosus 87 11.709
11
P AST005 Asthma 84 11.709
12
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 11.709
13
SKN016 Skin Disease 71 11.709
14
VSC007 Vascular Disease 70 11.709
15
P RSP003 Respiratory Failure 68 11.709
16
ACN011 Acne 65 11.709
17
P ALC004 Alcohol Abuse 62 11.709
18
ANR002 Aniridia 60 11.709
19
BRS051 Breast Disease 60 11.709
20
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 53 11.709
21
NNT017 Neonatal Adrenoleukodystrophy 51 11.709
22
c PRX045 Peroxisome Biogenesis Disorder 1b 49 11.709
23
ASB001 Asbestosis 43 11.709
24
FVS001 Favism 42 11.709
25
MCR018 Microcytic Anemia 38 11.709
26
PTY002 Pityriasis Versicolor 37 11.709
27
DBT007 Diabetic Cataract 36 11.709
28
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 9.561
29
P PRK057 Parkinson Disease, Late-Onset 73 9.561
30
P ADL010 Adult Respiratory Distress Syndrome 60 9.561
31
P AVS004 Avascular Necrosis of the Femoral Head 56 9.561
32
SCL003 Social Phobia 54 9.561
33
TXC002 Toxic Encephalopathy 53 9.561
34
TTR011 Tetraploidy 53 9.561
35
HYP141 Hyperphenylalaninemia 51 9.561
36
RTN003 Retinal Ischemia 51 9.561
37
c HMG001 Hemoglobin C Disease 50 9.561
38
PRN023 Prion Disease 50 9.561
39
PNM013 Pneumococcal Meningitis 50 9.561
40
CRY003 Cryptosporidiosis 49 9.561
41
MYC005 Myocardial Stunning 48 9.561
42
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 45 9.561
43
FTL030 Fetal Valproate Syndrome 45 9.561
44
SPR016 Spermatic Cord Torsion 43 9.561
45
MRR001 Merrf Syndrome 43 9.561
46
c CNG124 Congenital Rubella 43 9.561
47
PRX077 Peroxisomal Biogenesis Disorders 42 9.561
48
MYL013 Myeloperoxidase Deficiency 41 9.561
49
HYP107 Hyperornithinemia-Hyperammonemia-Homocitrullinemia Syndrome 41 9.561
50
PRX034 Peroxisome Disorders 40 9.561
51
HYP003 Hypermethioninemia 38 9.561
52
DBT081 Diabetic Encephalopathy 36 9.561
53
CSP003 Cisplatin Toxicity 35 9.561
54
MGK002 Megakaryocytic Tumor 34 9.561
55
PHT002 Photokeratitis 34 9.561
56
TXC008 Toxic Optic Neuropathy 33 9.561
57
SLF001 Sulfhemoglobinemia 33 9.561
58
URG001 Urogenital Tuberculosis 32 9.561
59
VTR002 Vitreous Syneresis 29 9.561
60
MNN024 Meningitis and Encephalitis 28 9.561
61
TTR001 Tetralogy of Fallot 70 6.760
62
P ORL007 Oral Cavity Cancer 55 6.760