Disease #00036 (BJS (Bjornstad syndrome (BJS)), OMIM:262000)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	BJS
Name	Bjornstad syndrome (BJS)
OMIM ID	262000
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BCS1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-30 16:23:34 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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