Oculocutaneous albinism type 1A (Q65037): Difference between revisions

@@ Property / CURIE @@
+CID11:ID_1168847652
@@ Property / CURIE: CID11:ID_1168847652 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1168847652
@@ Property / Canary Token: dki-india-ID_1168847652 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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-Timestamp
++2026-08-13T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
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@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank

Latest revision as of 12:45, 14 August 2026

OCA-1 is caused by mutation in the tyrosinase gene (TYR). OCA-1A is due to complete absence of TYR and a more severe clinical phenotype than OCA-1B.

Language	Label	Description	Also known as
default for all languages	ID_1168847652
English	Oculocutaneous albinism type 1A	OCA-1 is caused by mutation in the tyrosinase gene (TYR). OCA-1A is due to complete absence of TYR and a more severe clinical phenotype than OCA-1B.