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 91 13.521
3
ADR007 Adrenoleukodystrophy 71 13.521
4
WLS001 Wilson Disease 68 13.521
5
CHR012 Chronic Granulomatous Disease 62 13.521
6
P RFS001 Refsum Disease 57 13.521
7
P PNM006 Pneumoconiosis 48 13.521
8
P PRP023 Peripheral Neuropathy 41 13.521
9
P RHM011 Rheumatoid Arthritis 87 11.709
10
c SYS001 Systemic Lupus Erythematosus 84 11.709
11
P AST005 Asthma 77 11.709
12
P DBT085 Diabetes Mellitus, Insulin-Dependent 77 11.709
13
ANR002 Aniridia 62 11.709
14
SKN016 Skin Disease 58 11.709
15
ACN011 Acne 55 11.709
16
VSC007 Vascular Disease 55 11.709
17
P RSP003 Respiratory Failure 55 11.709
18
P ALC004 Alcohol Abuse 52 11.709
19
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 48 11.709
20
c PRX045 Peroxisome Biogenesis Disorder 1b 46 11.709
21
BRS051 Breast Disease 46 11.709
22
FVS001 Favism 44 11.709
23
ASB001 Asbestosis 42 11.709
24
NNT017 Neonatal Adrenoleukodystrophy 41 11.709
25
MCR018 Microcytic Anemia 38 11.709
26
PTY002 Pityriasis Versicolor 38 11.709
27
DBT007 Diabetic Cataract 30 11.709
28
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 76 9.561
29
P PRK057 Parkinson Disease, Late-Onset 69 9.561
30
P ADL010 Adult Respiratory Distress Syndrome 51 9.561
31
P AVS004 Avascular Necrosis of the Femoral Head 49 9.561
32
TTR011 Tetraploidy 48 9.561
33
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 47 9.561
34
FTL030 Fetal Valproate Syndrome 44 9.561
35
HYP141 Hyperphenylalaninemia 44 9.561
36
MRR001 Merrf Syndrome 43 9.561
37
RTN003 Retinal Ischemia 43 9.561
38
TXC002 Toxic Encephalopathy 43 9.561
39
PNM013 Pneumococcal Meningitis 43 9.561
40
c CNG124 Congenital Rubella 43 9.561
41
PRN023 Prion Disease 42 9.561
42
c HMG001 Hemoglobin C Disease 42 9.561
43
HYP107 Hyperornithinemia-Hyperammonemia-Homocitrullinemia Syndrome 42 9.561
44
CRY003 Cryptosporidiosis 41 9.561
45
SCL003 Social Phobia 41 9.561
46
MYC005 Myocardial Stunning 37 9.561
47
SPR016 Spermatic Cord Torsion 37 9.561
48
MYL013 Myeloperoxidase Deficiency 37 9.561
49
HYP003 Hypermethioninemia 35 9.561
50
PRX077 Peroxisomal Biogenesis Disorders 33 9.561
51
PHT002 Photokeratitis 32 9.561
52
SLF001 Sulfhemoglobinemia 32 9.561
53
URG001 Urogenital Tuberculosis 30 9.561
54
DBT081 Diabetic Encephalopathy 29 9.561
55
CSP003 Cisplatin Toxicity 27 9.561
56
TXC008 Toxic Optic Neuropathy 26 9.561
57
MGK002 Megakaryocytic Tumor 26 9.561
58
VTR002 Vitreous Syneresis 25 9.561
59
MNN024 Meningitis and Encephalitis 23 9.561
60
PRX034 Peroxisome Disorders 19 9.561
61
TTR001 Tetralogy of Fallot 66 6.760
62
P ORL007 Oral Cavity Cancer 45 6.760