Disease #06957 (SCOLIV (liver disease, severe congenital), OMIM:619991)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SCOLIV
Name	liver disease, severe congenital
OMIM ID	619991
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FOCAD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-08-19 11:45:21 +02:00 (CEST)
Date last edited	N/A

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