Disease #00345 (CFHD (deficiency, complement factor H (CFHD)), OMIM:609814)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CFHD
Name	deficiency, complement factor H (CFHD)
OMIM ID	609814
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	CFH
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-03-13 09:50:57 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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