Disease #04180 (AOS5 (Adams-Oliver syndrome, type 5 (AOS-5)), OMIM:616028)

Official abbreviation AOS5
Name Adams-Oliver syndrome, type 5 (AOS-5)
OMIM ID 616028
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NOTCH1
Associated tissues -
Disease features -
Remarks -
Date created 2015-02-07 16:01:19 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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