Search results for "[genes] HEXA"

32 hits were found for '[genes] HEXA'

# Family MCID Name MIFTS Score
1
P TYS001 Tay-Sachs Disease 71 26.706
2
P GNG009 Gangliosidosis 60 20.950
3
LYS002 Lysosomal Storage Disease 56 14.814
4
P MTC003 Metachromatic Leukodystrophy 70 12.829
5
c MCP037 Mucopolysaccharidosis is 67 12.829
6
c GNG001 Gangliosidosis Gm1 58 12.829
7
SND007 Sandhoff Disease, Infantile, Juvenile, and Adult Forms 56 12.829
8
c AMY091 Amyotrophic Lateral Sclerosis 1 79 10.475
9
P FCS002 Fucosidosis 56 10.475
10
c MNN025 Mannosidosis, Alpha-, Types I and Ii 53 10.475
11
LPD009 Lipid Storage Disease 52 10.475
12
c INH020 Inherited Metabolic Disorder 51 10.475
13
P LRY044 Larynx Cancer 51 10.475
14
MST001 Mast-Cell Sarcoma 49 10.475
15
SPH010 Sphingolipidosis 47 10.475
16
c MCL013 Mucolipidosis Iv 46 10.475
17
INC022 Inclusion-Cell Disease 44 10.475
18
c MNN044 Mannosidosis, Beta 43 10.475
19
NNL001 Non-Langerhans-Cell Histiocytosis 43 10.475
20
PRG007 Progressive Bulbar Palsy 41 10.475
21
INT042 Internuclear Ophthalmoplegia 41 10.475
22
CHL012 Childhood Disintegrative Disease 38 10.475
23
c JVN006 Juvenile Spinal Muscular Atrophy 37 10.475
24
LBM003 Lobomycosis 37 10.475
25
c GNG010 Gangliosidosis Gm2 37 10.475
26
CRB018 Cerebral Lipidosis 32 10.475
27
c TYS006 Tay-Sachs Disease, B Variant, Adult Form 14 7.407
28
c TYS005 Tay-Sachs Disease, B1 Variant 14 7.407
29
c TYS004 Tay-Sachs Disease, B Variant, Infantile Form 13 7.407
30
c TYS003 Tay-Sachs Disease, B Variant, Juvenile Form 9 7.407
31
JVN021 Juvenile Hexosaminidase a Deficiency 7 7.407
32
CHR335 Chronic and Adult-Onset Hexosaminidase a Deficiency 4 7.407