www.fgks.org   »   [go: up one dir, main page]

Disease #00989 (BOS3 (branchiootic syndrome, type 3), OMIM:608389)

Official abbreviation BOS3
Name branchiootic syndrome, type 3
OMIM ID 608389
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SIX1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-01-23 14:00:37 +01:00 (CET)