Disease #04532 (SCN6 (neutropenia, severe congenital, type 6, autosomal recessive (SCN-6)), OMIM:616022)

Official abbreviation	SCN6
Name	neutropenia, severe congenital, type 6, autosomal recessive (SCN-6)
OMIM ID	616022
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	JAGN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD