Disease #05826 (BBS21 (Bardet-Biedl syndrome, type 21 (BBS21)), OMIM:617406)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	BBS21
Name	Bardet-Biedl syndrome, type 21 (BBS21)
OMIM ID	617406
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	C8orf37
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-08-30 11:05:30 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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