Oca1 albinism. Medical search. Frequent questions

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Anatomy11

Melanosomes Melanocytes Fundus Oculi Chromosomes, Human, Pair 15 Optic Chiasm Fovea Centralis Pigment Epithelium of Eye Melanophores Hair Eye Visual Pathways

Organisms2

Characidae Pontederiaceae

Diseases20

Albinism Albinism, Oculocutaneous Hermanski-Pudlak Syndrome Hypopigmentation Nystagmus, Pathologic Nystagmus, Congenital Piebaldism Albinism, Ocular Pigmentation Disorders Chediak-Higashi Syndrome Photophobia Genetic Diseases, X-Linked Chondrodysplasia Punctata Platelet Storage Pool Deficiency Ichthyosis Kallmann Syndrome Prader-Willi Syndrome Sunburn Hemorrhagic Disorders Iris Diseases

Chemicals and Drugs14

Monophenol Monooxygenase Membrane Transport Proteins Melanins Receptor, Melanocortin, Type 1 Eye Proteins Oxidoreductases Membrane Glycoproteins Catechol Oxidase Antigens, Neoplasm Sunscreening Agents Membrane Proteins Dihydroxyphenylalanine Adaptor Protein Complex beta Subunits Ceroid

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

Skin Pigmentation Pigmentation Pedigree Electronystagmography DNA Mutational Analysis Visual Acuity

Psychiatry and Psychology1

Phenomena and Processes17

Eye Color Skin Pigmentation Pigmentation Hair Color Evoked Potentials, Visual Mutation Caves Chromosomes, Human, Pair 15 Phenotype Polymorphism, Single-Stranded Conformational Visual Acuity Homozygote Frameshift Mutation Exons Alleles Genes, Recessive Heterozygote

Anthropology, Education, Sociology and Social Phenomena2

Folklore Social Alienation

Health Care1

Geographicals3

Guinea Puerto Rico Zimbabwe

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Health Care Geographicals

Albinism Albinism, Oculocutaneous Monophenol Monooxygenase Hermanski-Pudlak Syndrome Hypopigmentation Eye Color Nystagmus, Pathologic Melanosomes Folklore Nystagmus, Congenital Skin Pigmentation Melanocytes Pigmentation Membrane Transport Proteins Melanins Hair Color Piebaldism Receptor, Melanocortin, Type 1 Albinism, Ocular Characidae Pigmentation Disorders Evoked Potentials, Visual Chediak-Higashi Syndrome Photophobia Mutation Pedigree Eye Proteins Electronystagmography Pontederiaceae Oxidoreductases Genetic Diseases, X-Linked Membrane Glycoproteins Social Alienation Catechol Oxidase Caves Chondrodysplasia Punctata Fundus Oculi Chromosomes, Human, Pair 15 Optic Chiasm Fovea Centralis Phenotype Platelet Storage Pool Deficiency DNA Mutational Analysis Polymorphism, Single-Stranded Conformational Pigment Epithelium of Eye Guinea Visual Acuity Ichthyosis Kallmann Syndrome Homozygote Prader-Willi Syndrome Puerto Rico Frameshift Mutation Exons Melanophores Antigens, Neoplasm Sunscreening Agents Alleles Membrane Proteins Genes, Recessive Zimbabwe Dihydroxyphenylalanine Hair Adaptor Protein Complex beta Subunits Eye Sunburn Hemorrhagic Disorders Heterozygote Iris Diseases Ceroid Visual Pathways

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