(albinism)

  • 81Hypopigmentation — Classification and external resources Hypopigmentation in vitiligo. ICD 10 L80, L81.5 L81.6 ICD 9 …

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  • 82Tyrosinase — monophenol monooxygenase Identifiers EC number 1.14.18.1 CAS number 9002 10 2 …

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  • 83Leucism — is a condition characterized by reduced pigmentation in animals. Unlike albinism, it is caused by a reduction in all types of skin pigment, not just melanin.Leucism is a general term for the phenotype resulting from defects in pigment cell… …

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  • 84Depigmentation — is the lightening of the skin, or loss of pigment. Depigmentation of the skin can be caused by a number of local and systemic conditions. The pigment loss can be partial (injury to the skin) or complete (caused by vitiligo). It can be temporary… …

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  • 85syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …

    Medical dictionary

  • 86Okulokutaner Albinismus Typ 1 — OCA1 ist für viele der am stärksten ausgeprägten Fälle von Albinismus verantwortlich Okulokutaner Albinismus Typ 1, abgekürzt OCA 1 ist eine Form des Albinismus, die auf Mutationen des TYR Gens (codierend für Tyrosinase) zurückgeht. Eine andere… …

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  • 87Phenylketonuria — PKU redirects here. For other uses, see PKU (disambiguation). Phenylketonuria Classification and external resources ICD 10 E70.0 ICD 9 …

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  • 88Acanthosis nigricans — Classification and external resources Acanthosis nigricans on axilla ICD 10 L …

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  • 89Ornithine transcarbamylase deficiency — Classification and external resources Ornithine ICD 10 E …

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  • 90Hyperpigmentation — Classification and external resources ICD 10 L81.0 L81.4 ICD 9 709.0 DiseasesDB …

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