Disease #05832 (SPH2 (spherocytosis, type 2 (SPH2)), OMIM:616649)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPH2
Name	spherocytosis, type 2 (SPH2)
OMIM ID	616649
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SPTB
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-09-15 10:10:43 +02:00 (CEST)
Date last edited	N/A

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