Search results for "[genes] CTSA"

30 hits were found for '[genes] CTSA'

# Family MCID Name MIFTS Score
1
GLC012 Galactosialidosis 47 24.698
2
c MCP037 Mucopolysaccharidosis is 64 14.893
3
c MCP004 Mucopolysaccharidosis Iv 60 14.893
4
P TYS001 Tay-Sachs Disease 71 12.898
5
P MCL013 Mucolipidosis Iv 62 12.898
6
P FCS002 Fucosidosis 57 12.898
7
c MNN025 Mannosidosis, Alpha-, Types I and Ii 55 12.898
8
ASP002 Aspartylglucosaminuria 55 12.898
9
PLV003 Pelvic Inflammatory Disease 54 12.898
10
LYS002 Lysosomal Storage Disease 52 12.898
11
HML015 Hemolytic Anemia Due to Triosephosphate Isomerase Deficiency 46 12.898
12
SPH010 Sphingolipidosis 45 12.898
13
c MNN044 Mannosidosis, Beta 44 12.898
14
ANG016 Angiokeratoma 40 12.898
15
c ACT081 Acute Salpingitis 35 12.898
16
P GNG010 Gangliosidosis Gm2 32 12.898
17
ATR003 Atrophic Rhinitis 31 12.898
18
c CHR099 Chronic Salpingitis 30 12.898
19
GLY031 Glycoproteinosis 28 12.898
20
c CHR054 Chronic Closed-Angle Glaucoma 25 12.898
21
c RNG016 Ring Chromosome 20 24 12.898
22
c CHR017 Chronic Gonococcal Salpingitis 24 12.898
23
P ACT028 Acute Closed-Angle Glaucoma 22 12.898
24
MYC001 Myoclonic Cerebellar Dyssynergia 20 12.898
25
P ACT023 Acute Gonococcal Salpingitis 11 12.898
26
P SLD010 Sialidosis, Type I 54 10.531
27
P MNN018 Mannosidosis 47 10.531
28
INC022 Inclusion-Cell Disease 46 10.531
29
c ATS345 Autosomal Dominant Nonsyndromic Deafness 69 29 10.531
30
c CRN222 Corneal Endothelial Dystrophy 1, Autosomal Dominant 23 10.531