Yellow oculocutaneous albinism (Q93415): Difference between revisions

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O OCA amarelo é uma variante do OCA-1B na qual os pacientes nascem sem pigmento e com graves problemas visuais associados, mas desenvolvem alguma pigmentação, principalmente feomelanina amarelo-avermelhada, desde a primeira infância. Esta forma é relatada principalmente na população Amish da América do Norte.
description / endescription / en
 
Yellow OCA is a variant of OCA-1B where patients are born with no pigment and associated severe visual problems, but develop some pigmentation, principally yellow-red phaeomelanin, from early childhood. This form is primarily reported in the Amish population of North America.
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Property / Canonical URI: https://id.who.int/icd/entity/1816007840 / rank
 
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CID11:ID_1816007840
Property / CURIE: CID11:ID_1816007840 / rank
 
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dki-india-ID_1816007840
Property / Canary Token: dki-india-ID_1816007840 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 15 August 2026 / rank
 
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Latest revision as of 08:31, 16 August 2026

Yellow OCA is a variant of OCA-1B where patients are born with no pigment and associated severe visual problems, but develop some pigmentation, principally yellow-red phaeomelanin, from early childhood. This form is primarily reported in the Amish population of North America.
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ID_1816007840
    English
    Yellow oculocutaneous albinism
    Yellow OCA is a variant of OCA-1B where patients are born with no pigment and associated severe visual problems, but develop some pigmentation, principally yellow-red phaeomelanin, from early childhood. This form is primarily reported in the Amish population of North America.

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      CID11:ID_1816007840
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      dki-india-ID_1816007840
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      Concluído
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      15 August 2026
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