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611409
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OCA2 GENE
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Neoplasms
Neoplasms by Histologic Type
Neoplasms, Germ Cell and Embryonal
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Melanoma, Experimental
Neoplasms, Nerve Tissue
Neuroectodermal Tumors
Neuroendocrine Tumors
Melanoma
Melanoma, Experimental
Nevi and Melanomas
Melanoma
Melanoma, Experimental
Nevus
Nevus, Pigmented
Neoplasms by Site
Skin Neoplasms
Neoplasms, Experimental
Melanoma, Experimental
Musculoskeletal Diseases
Muscular Diseases
Nervous System Diseases
Central Nervous System Diseases
Movement Disorders
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Prader-Willi Syndrome
Neuromuscular Diseases
Muscular Diseases
Eye Diseases
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Heart Block
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Hemoglobinopathies
Anemia, Sickle Cell
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Prader-Willi Syndrome
Chromosome Disorders
Prader-Willi Syndrome
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Chromosome Disorders
Prader-Willi Syndrome
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Hemoglobinopathies
Anemia, Sickle Cell
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Skin and Connective Tissue Diseases
Skin Diseases
Photosensitivity Disorders
Sunburn
Pigmentation Disorders
Hyperpigmentation
Melanosis
Hypopigmentation
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Skin Neoplasms
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Albinism, Oculocutaneous
Nutrition Disorders
Overnutrition
Obesity
Prader-Willi Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Arrhythmias, Cardiac
Heart Block
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Chromosome Inversion
Translocation, Genetic
Death
Death, Sudden
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Wounds and Injuries
Burns
Sunburn
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