Disease #07053 (BRYLIB1 (Bryant-Li-Bhoj neurodevelopmental syndrome, type 1), OMIM:619720)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	BRYLIB1
Name	Bryant-Li-Bhoj neurodevelopmental syndrome, type 1
OMIM ID	619720
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	H3F3A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-12-24 13:22:19 +01:00 (CET)
Date last edited	2023-12-24 13:24:18 +01:00 (CET)

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