31 Bilder zum Thema "autosomal recessive" bei ClipDealer

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Paper with words Werner syndrome and glasses.
Tay-Sachs disease, 3D illustration. A genetic disorder that progressively destroys brain neurons, is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A
Sickle Cells Blocking Blood Flow
Coronal sections of a healthy brain and a brain in Huntington's disease showing enlarged anterior horns of the lateral ventricles, degeneration and atrophy of the dorsal striatum, 3D illustration
Dorsal striatum, caudate nucleus and putamen, highlighted in the brain of a person with Huntington's disease and close-up view of neuronal degradation, conceptual 3D illustration
Autosomal Dominant Disorder concept
Molecule of beta-hexosaminidase A enzyme, or HEXA, 3D illustration. Mutations in the gene encoding HEXA decrease the hydrolysis of GM2 gangliosides, which is the main cause of Tay-Sachs disease
Heterozygous parent gene in chromosomes, 3d rendering
Book with title Joubert Syndrome on a table.
Eye retina in Tay-Sachs disease, 3D illustration with so-called cherry-red spot. A genetic disorder that progressively destroys brain neurons, is caused by a genetic mutation in the HEXA gene
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
Sickle Cell Anemia concept
Phenylketonuria
Dorsal striatum, caudate nucleus and putamen, highlighted in the brain of a person with Huntington's disease and close-up view of neuronal inclusions, conceptual 3D illustration
Paper with words Sanfilippo syndrome and glasses. Medical concept.
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
Hereditary Disorder - medical concept
Cystic fibrosis
3D rendering SCID word - severe combined immunodeficiency concept letter design isolated on white background
Autosomal recessive bestrophinopathy, ophthalmoscope view, scientific illustration showing accumulation of lipofuscin deposits around and beyond the macula leading to progressive damage to the retina
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
Diagnostic form with Diagnosis Tay Sachs disease.
Link between genetics and the cystic fibrosis disorder, also known as mucoviscidosis
Neuroacanthocytosis, Chorea acanthocytosis, a neurodegenerative disease due to mutation in the gene VPS13A, it is marked by presence of acanthocytes in blood and choreiform movements, 3D illustration
Neuroacanthocytosis, Chorea acanthocytosis, a neurodegenerative disease due to mutation in the gene VPS13A, it is marked by presence of acanthocytes in blood and choreiform movements, 3D illustration
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
Eye retina in sphingolipid storage diseases, 3D illustration. Macular cherry red spot. Tay-Sachs disease and Niemann Pick disease
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomes
Sickle Cells Blocking Blood Flow - isolated on white
Homozygous parent gene in chromosomes, 3d rendering

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