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Stock image Autosomal Recessive

stock vector Autosomal Recessive Hereditary Trait infographic diagram including parents father and mother probability of son and daughter to be affected unaffected or carrier for genetic science education

Autosomal Recessive Hereditary Trait Infographic Diagram Including Parents Father And Mother Probability Of Son And Daughter To Be Affected Unaffected Or Carrier For Genetic Science Education

Vector, 0.4MB, 1694 × 2420 eps
stock vector Autosomal Dominant Hereditary Trait infographic diagram including parents father and mother probability of son and daughter to be affected or unaffected by mutated gene for genetic science education

Autosomal Dominant Hereditary Trait Infographic Diagram Including Parents Father And Mother Probability Of Son And Daughter To Be Affected Or Unaffected By Mutated Gene For Genetic Science Education

Vector, 0.38MB, 1650 × 2499 eps
stock image Paper with words Werner syndrome and glasses.

Paper With Words Werner Syndrome And Glasses.

Image, 7.48MB, 5500 × 3667 jpg
stock image 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

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

Image, 24.4MB, 14000 × 8436 jpg
stock image Sickle Cells Blocking Blood Flow

Sickle Cells Blocking Blood Flow

Image, 9.94MB, 6000 × 4500 jpg
stock image 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

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

Image, 10.57MB, 11104 × 6246 jpg
stock vector Polycystic kidney disease and healthy kidney. medical infographics. Vector illustration

Polycystic Kidney Disease And Healthy Kidney. Medical Infographics. Vector Illustration

Vector, 12.09MB, 5210 × 4000 eps
stock image 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

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

Image, 12.32MB, 7814 × 5210 jpg
stock image Autosomal Dominant Disorder concept

Autosomal Dominant Disorder Concept

Image, 2.43MB, 4500 × 3000 jpg
stock image 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

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

Image, 6.4MB, 5000 × 5000 jpg
stock image Heterozygous parent gene in chromosomes, 3d rendering

Heterozygous Parent Gene In Chromosomes, 3d Rendering

Image, 2.97MB, 6000 × 4000 jpg
stock vector Polycystic kidney disease.Normal and polycystic kidneys.Realistic organs

Polycystic Kidney Disease.Normal And Polycystic Kidneys.Realistic Organs

Vector, 2.63MB, 8334 × 8334 eps
stock image Book with title Joubert Syndrome on a table.

Book With Title Joubert Syndrome On A Table.

Image, 10.58MB, 5500 × 3667 jpg
stock image 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

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

Image, 3.82MB, 5000 × 5000 jpg
stock vector Sex-linked Dominant Hereditary Trait infographic diagram showing father with abnormal gene on X sex chromosome while mother has normal ones for genetics and medical science education

Sex-linked Dominant Hereditary Trait Infographic Diagram Showing Father With Abnormal Gene On X Sex Chromosome While Mother Has Normal Ones For Genetics And Medical Science Education

Vector, 0.34MB, 2022 × 2063 eps
stock vector 3D Isometric Flat Vector Conceptual Illustration of Autosomal Recessive Inheritance, Dominant and Recessive Genes

3D Isometric Flat Vector Conceptual Illustration Of Autosomal Recessive Inheritance, Dominant And Recessive Genes

Vector, 1.81MB, 6000 × 4000 eps
stock image 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

Image, 7.14MB, 7200 × 4050 jpg
stock image Sickle Cell Anemia concept

Sickle Cell Anemia Concept

Image, 2.41MB, 4500 × 3000 jpg
stock image Phenylketonuria

Phenylketonuria

Image, 1.35MB, 3228 × 2469 jpg
stock vector Cystic Fibrosis (mucoviscidosis) inheritance

Cystic Fibrosis (mucoviscidosis) Inheritance

Vector, 2.33MB, 6000 × 4243 eps
stock image 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

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

Image, 7.98MB, 6000 × 6000 jpg
stock image Paper with words Sanfilippo syndrome  and glasses. Medical concept.

Paper With Words Sanfilippo Syndrome And Glasses. Medical Concept.

Image, 8.12MB, 5500 × 3667 jpg
stock image 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

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

Image, 28.81MB, 11622 × 8072 jpg
stock image Hereditary Disorder - medical concept

Hereditary Disorder - Medical Concept

Image, 2.42MB, 4500 × 3000 jpg
stock image Cystic fibrosis

Cystic Fibrosis

Image, 1.69MB, 3228 × 2469 jpg
stock image 3D rendering SCID word -  severe combined immunodeficiency  concept letter design isolated on white background

3D Rendering SCID Word - Severe Combined Immunodeficiency Concept Letter Design Isolated On White Background

Image, 1.17MB, 4000 × 2043 jpg
stock vector genetic inheritance.

Genetic Inheritance.

Vector, 4.4MB, 6268 × 6268 eps
stock vector Features of inheritance. chromosome theory of inheritance. Cell with parents genome and track the inheritance patterns of traits like Skin, Hair and Eye color, Genetic disorder and height. Mendel's law about Segregation, Independent Assortment and Pr

Features Of Inheritance. Chromosome Theory Of Inheritance. Cell With Parents Genome And Track The Inheritance Patterns Of Traits Like Skin, Hair And Eye Color, Genetic Disorder And Height. Mendel's Law About Segregation, Independent Assortment And Pr

Vector, 12.68MB, 4444 × 4443 eps
stock image 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

Image, 6MB, 7200 × 4050 jpg
stock image Autosomal recessive bestrophinopathy, ophthalmoscope view, scientific illustration showing accumulation of lipofuscin deposits around and beyond the macula leading to progressive damage to the retina

Autosomal Recessive Bestrophinopathy, Ophthalmoscope View, Scientific Illustration Showing Accumulation Of Lipofuscin Deposits Around And Beyond The Macula Leading To Progressive Damage To The Retina

Image, 3MB, 5000 × 5000 jpg
stock vector Heterozygous vs homozygous parent gene differences comparison outline diagram

Heterozygous Vs Homozygous Parent Gene Differences Comparison Outline Diagram

Vector, 5.7MB, 5500 × 3184 eps
stock image Diagnostic form with Diagnosis Tay Sachs disease.

Diagnostic Form With Diagnosis Tay Sachs Disease.

Image, 9.38MB, 5200 × 3467 jpg
stock image Link between genetics and the cystic fibrosis disorder, also known as mucoviscidosis

Link Between Genetics And The Cystic Fibrosis Disorder, Also Known As Mucoviscidosis

Image, 0.85MB, 4000 × 3100 jpg
stock image Tourettes Disorder - learn, study and inspect it. Taking a closer look at tourettes disorder. A magnifying glass enlarging word 'tourettes disorder' written on a blackboard

Tourettes Disorder - Learn, Study And Inspect It. Taking A Closer Look At Tourettes Disorder. A Magnifying Glass Enlarging Word 'tourettes Disorder' Written On A Blackboard

Image, 2.71MB, 5472 × 3648 jpg
stock image 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

Image, 13.25MB, 9117 × 5128 jpg
stock image 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

Image, 16.95MB, 10712 × 5356 jpg
stock image 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

Image, 8.36MB, 6000 × 6000 jpg
stock image 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

Image, 8.36MB, 6000 × 6000 jpg
stock image 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

Image, 6.66MB, 7200 × 4050 jpg
stock image Sickle Cells Blocking Blood Flow - isolated on white

Sickle Cells Blocking Blood Flow - Isolated On White

Image, 9.95MB, 6000 × 4500 jpg
stock vector Genetic inheritance as two alleles in gene pair are inherited outline diagram. Labeled educational scheme with genetic interaction and effect for offspring vector illustration. Biological explanation

Genetic Inheritance As Two Alleles In Gene Pair Are Inherited Outline Diagram. Labeled Educational Scheme With Genetic Interaction And Effect For Offspring Vector Illustration. Biological Explanation

Vector, 5.64MB, 4000 × 4222 eps
stock image Eye retina in sphingolipid storage diseases, 3D illustration. Macular cherry red spot. Tay-Sachs disease and Niemann Pick disease

Eye Retina In Sphingolipid Storage Diseases, 3D Illustration. Macular Cherry Red Spot. Tay-Sachs Disease And Niemann Pick Disease

Image, 2.54MB, 5000 × 5000 jpg
stock image Homozygous parent gene in chromosomes, 3d rendering

Homozygous Parent Gene In Chromosomes, 3d Rendering

Image, 3.01MB, 6000 × 4000 jpg
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