Disease #05977 (CCHS3 (hypoventilation, central, syndrome, congenital, type 3 (CCHS3)), OMIM:619483)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CCHS3
Name	hypoventilation, central, syndrome, congenital, type 3 (CCHS3)
OMIM ID	619483
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LBX1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-10-18 22:15:09 +02:00 (CEST)
Date last edited	N/A

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