Disease #03204 (AHUS2 (hemolyticuremic syndrome, atypical, type 2 (AHUS2)), OMIM:612922)

Global Variome shared LOVD

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Official abbreviation	AHUS2
Name	hemolyticuremic syndrome, atypical, type 2 (AHUS2)
OMIM ID	612922
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CD46
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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