Griscelli syndrome type 2 (Q88711): Difference between revisions

Revision as of 15:06, 15 August 2026

This type, caused by mutations in RAB27A presents with pigmentary dilution and immunodeficiency

Language	Label	Description	Also known as
default for all languages	ID_1836541365
English	Griscelli syndrome type 2	This type, caused by mutations in RAB27A presents with pigmentary dilution and immunodeficiency

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CID11:ID_1836541365

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dki-india-ID_1836541365

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Concluído

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Revision as of 15:06, 15 August 2026 Determinaradmin (talk \| contribs) Bureaucrats, Interface administrators, Administrators 679,186 edits ‎Changed an Item ← Older edit	Revision as of 15:06, 15 August 2026 Determinaradmin (talk \| contribs) Bureaucrats, Interface administrators, Administrators 679,186 edits ‎Changed an Item Newer edit →
	Property / Verification Status
		Concluído
	Property / Verification Status: Concluído / rank
		Normal rank