3d
ashkenazi
autosomal
baby
betahexosaminidase a
brain
cherry red spot
child
chromosome 15
congenital
deficiency
demyelination
diagram
disease
disorder
dna
enlarged
enzyme
ganglioside
gangliosidosis
gene
gene mutation
genetic
gm2
gm2 ganglioside
hexa
hexa gene
hexosaminidase a
illustration
infant
inherited
jew
lipid
lysosomal
lysosome
macrocephaly
metabolic
metabolism
molecule
mutation
neurology
neuron
polypeptide
recessive
retina
sphingolipidosis
storage
storage disease
taysachs
tsd
定額
Tay-Sachs disease, a lysosomal storage genetic disorder, 3D illustration. A child with macrocephaly, and close-up view of swollen neurons with lamellar inclusions due to accumulation of gangliosidesの素材 [FY310177151623]
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