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Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Albinism > Albinism, Oculocutaneous
Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Albinism > Albinism, Oculocutaneous
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Eye Diseases, Hereditary > Albinism > Albinism, Oculocutaneous
Eye Diseases > Eye Diseases, Hereditary > Albinism > Albinism, Oculocutaneous
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Albinism > Albinism, Oculocutaneous
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Amino Acid Metabolism, Inborn Errors > Albinism > Albinism, Oculocutaneous
... > Pathological Conditions, Signs and Symptoms > Pathologic Processes > Pigmentation Disorders > Hypopigmentation > Albinism > Albinism, Oculocutaneous
... > Skin and Connective Tissue Diseases > Skin Diseases > Pigmentation Disorders > Hypopigmentation > Albinism > Albinism, Oculocutaneous

Término preferido

Albinism, Oculocutaneous  

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Tipo

  • mesh:Descriptor

Definición

  • Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types.

Concepto genérico

Conceptos específicos

Etiquetas alternativas

  • Oculocutaneous Albinism

En otras lenguas

  • Albinisme oculocutané

    francés

  • Albinisme cutanéo-oculaire
  • Albinisme oculo-cutané
  • AOC (Albinisme Oculo-Cutané)

URI

http://data.loterre.fr/ark:/67375/JVR-NKC9NV75-L

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