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Hemophilia blood clotting stages. Vessel cuts. Medical infographic in realistic style. Editable vector illustration in red colours isolated on light background. Scientific and healthcare concept
Hemophilia blood clotting stages. Vessel cuts. Medical infographic in realistic style. Editable vector illustration in red colours isolated on dark grey background. Scientific and healthcare concept
Conceptual vector illustration. The medical diagnosis. Stop myopathy.
Seborrhei Dermatitis - skin disease. Ear Canal Eczema. Redness of external ear canal psoriasis. Seborrheic dermatitis on the scalp (dandruff). Seborrheic dermatitis along the nasolabial folds
Like mother, like daughter concept. Family history. Genetics, heredity image. Two of a kind. Editable vector illustration in pastel colors isolated on a white background. Flat cartoon style
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 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
Sickle cell disease. SCD is a disorder inherited from a person's parents. anaemia, or anemia. Comparison and difference between blood vessel and erythrocytes of healthy person and abnormal red blood cells sticking at the branching point In a blood ve
Vector illustration on the theme of world Thalassemia day observed on May 8th every year. Thalassemias are inherited blood disorders characterized by decreased hemoglobin production
World Autism Awareness Day concept with multicolored ribbon. Colorful vector illustration for web and printing.
Sickle cell disease. SCD is a blood disorder inherited from a person's parents. sickle cell anaemia. Comparison and difference between normal erythrocytes and sickle-shaped red blood cells. Vector illustration
Muscular dystrophy icon. Trendy flat vector Muscular dystrophy icon on white background from Diseases collection, vector illustration can be use for web and mobile, eps10
Vector dementia icon in outline style. Medical editable illustration in pink color isolated on a white background. Useful element for logotype, symbol, pictogram and ad graphic design.
World hemophilia day illustration vector
Hypertrophic Cardiomyopathy icon in vector. Logotype
Marfan syndrome poster. Thoracic and cardiac manifestations. Chest cavity with enlarged aortic root, dilated aorta, mitral valve prolapse. Deformed ribcage, pectus excavatum or pectus carinatum vector
Marfan syndrome poster. Thoracic and cardiac manifestations. Chest cavity with enlarged aortic root, dilated aorta, mitral valve prolapse. Deformed ribcage, pectus excavatum or pectus carinatum vector
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Autosomal dominant inheritance of Marfan syndrome. One parent with a mutated FBN1 gene on chromosome 15 can pass the disorder to offspring. Family tree with affected and unaffected babies flat vector
World Thalassemia Day is observed every year on May 8th to commemorate Thalassemia victims and to encourage those who struggle to live with the disease. Vector illustration
Polycystic kidney disease and healthy kidney. medical infographics. Vector illustration.
Duchenne muscular dystrophy inheritance pattern. Hereditary neuromuscular disease. Progressive muscle fiber degeneration and weakness. Affected, carriers or healthy chromosomes vector illustration.
World Hemophilia Day background Vector illustration
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Autosomal dominant inheritance of Marfan syndrome. One parent with a mutated FBN1 gene on chromosome 15 can pass the disorder to offspring. Family tree with affected and unaffected babies flat vector
Autosomal dominant inheritance of Marfan syndrome. One parent with a mutated FBN1 gene on chromosome 15 can pass the disorder to offspring. Family tree with affected and unaffected babies flat vector
Thrombophilia Awareness Month background design with Red silk ribbon.
Genetic testing abstract concept vector illustration. Genetic blood testing method, DNA ancestry test, laboratory diagnosis, medical screening technology, inherited disorder abstract metaphor.
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Muscular dystrophy black glyph icon. Genetic disorder. Progressive muscle degeneration and weakness. Neuromuscular disease. Silhouette symbol on white space. Vector isolated illustration
Rare chromosome disorder icon. Editable stroke. Vector illustration. Structural chromosomal anomaly. Used in genetics, diagnostics. Cytogenetics, rare disease education concept
Acanthosis nigricans. Thickened, velvety and relatively darker areas of skin on the neck. The most common site of acanthosis nigricans. type 2 diabetes. Cushing's syndrome. faulty gene inherited. Vector illustration
Multiple sclerosis factors as MS disease risks and causes outline diagram. Labeled educational scheme with immunological, infectious, environmental or genetic health impact issues vector illustration
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Marfan syndrome disease. Human karyotype with emphasis on chromosome 15, FBN1 gene mutation. Educational genetic diagram, autosomal dominant inheritance pattern, connective tissue disorder flat vector
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Human silhouette with a silhouette affected by Marfan syndrome and normal body. Physical traits such as tall, slender body, long limbs, scoliosis. Chest deformity, pectus excavatum, and arachnodactyly
Marfan syndrome poster. Thoracic and cardiac manifestations. Chest cavity with enlarged aortic root, dilated aorta, mitral valve prolapse. Deformed ribcage, pectus excavatum or pectus carinatum vector
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Smartphone screen with symptoms of Marfan syndrome. Aortic dilation, chest deformity, long fingers, scoliosis, and eye problems. Surrounding the phone are pills, medication and bottles flat vector
Kidney Cyst vector illustration
Thalassemia. Close-up of normal red blood cells, and damaged blood cells. Mediterranean anemia. Inherited blood disorders that result in abnormal hemoglobin. Vector illustration
Primary Lymphedema stages. Lymphatic system disfunction. Elephantiasis, legs swelling disease. Young girl wearing compression stocking.
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Autosomal dominant inheritance of Marfan syndrome. One parent with a mutated FBN1 gene on chromosome 15 can pass the disorder to offspring. Family tree with affected and unaffected babies flat vector
Autosomal dominant inheritance of Marfan syndrome. One parent with a mutated FBN1 gene on chromosome 15 can pass the disorder to offspring. Family tree with affected and unaffected babies flat vector
Sickle cell disease. SCD. Normal erythrocytes and sickle cells on blood flow. red background. Anemia or anaemia. blood disorders. Vector poster
Red ribbon with World Thalassemia Day message on dark gradient background. Emotional symbol for blood disorder awareness, support, genetic illness. Glossy 3D vector illustration
Marfan syndrome poster. Thoracic and cardiac manifestations. Chest cavity with enlarged aortic root, dilated aorta, mitral valve prolapse. Deformed ribcage, pectus excavatum or pectus carinatum vector
Marfan syndrome poster. Thoracic and cardiac manifestations. Chest cavity with enlarged aortic root, dilated aorta, mitral valve prolapse. Deformed ribcage, pectus excavatum or pectus carinatum vector
Marfan syndrome disease. Human karyotype with emphasis on chromosome 15, FBN1 gene mutation. Educational genetic diagram, autosomal dominant inheritance pattern, connective tissue disorder flat vector
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Marfan syndrome disease. Human karyotype with emphasis on chromosome 15, FBN1 gene mutation. Educational genetic diagram, autosomal dominant inheritance pattern, connective tissue disorder flat vector
Genetic Research Double Helix Icon. It represents scientific inquiry into inherited conditions and breakthroughs in biological understanding. The vibrant colors evoke progress and support for health.
Vector illustration of polydactyly before and after surger
World Thalassemia Day is observed each year on May 8th to commemorate Thalassemia victims and to encourage those who struggle to live with the disease. Vector illustration.
Marfan syndrome anatomical icons with common symptoms. Tall body, long limbs and fingers, scoliosis, pectus excavatum, flat feet. Heart, eye, lungs problems, hypermobile joints vector illustration
Marfan syndrome finger length test. Arachnodactyly concept. Visual demonstrations of Steinberg sign, thumb protrusion from a clenched fist. Anatomical drawings of hand and fingers vector illustration
3d blue human stomach with magnifying glass and DNA helix inside. Genetic analysis of gastric tissue, hereditary disease detection concept. Low poly digital futuristic style, wireframe. Vector.
Marfan syndrome finger length test. Arachnodactyly and pectus excavatum. Steinberg sign concept, thumb protrusion from a clenched fist. Anatomical drawings of hand and fingers vector illustration
Marfan syndrome disease. Human karyotype with emphasis on chromosome 15, FBN1 gene mutation. Educational genetic diagram, autosomal dominant inheritance pattern, connective tissue disorder flat vector
Autosomal dominant inheritance of Marfan syndrome. One parent with a mutated FBN1 gene on chromosome 15 can pass the disorder to offspring. Family tree with affected and unaffected babies flat vector
Marfan syndrome disease poster. Human body silhouette, aortic root dilation and heart complications. FBN1 gene mutation on chromosome 15. Fingers with arachnodactyly medical vector illustration