3d
alpha
autosomal
background
betahexosaminidase a
brain
chemical
congenital
deficiency
demyelination
diagram
disease
disorder
dna
enzyme
gangliosidosis
gene mutation
genetic
gm2
gm2 ganglioside
hexa
hexa gene
hexosaminidase a
human
illustration
infancy
infant
inherited
lipid
lysosomal
lysosome
medical
metabolic
molecular
molecule
neurology
neuron
ocular
ophthalmology
pathology
polypeptide
rare
recessive
science
sphingolipidosis
storage
storage disease
structure
taysachs
tsd
定額
Tay-Sachs disease, 3D illustration. A genetic disorder that progressively destroys brain neurons, is caused by a genetic mutation in the HEXA gene leading to deficiency of hexosaminidase A enzymeの素材 [FY310176957550]
この写真素材のタグ
最近チェックした素材