Disease #07271 (MHC2D2 (MHC class II deficiency, type 2), OMIM:620815)

Global Variome shared LOVD

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Official abbreviation	MHC2D2
Name	MHC class II deficiency, type 2
OMIM ID	620815
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RFXANK
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-07-02 14:41:57 +02:00 (CEST)
Date last edited	N/A

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