Disease #00313 (DESMD (desmoid disease, hereditary), OMIM:135290)

Official abbreviation DESMD
Name desmoid disease, hereditary
OMIM ID 135290
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene APC
Associated tissues -
Disease features -
Remarks -
Date created 2014-01-27 14:57:06 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)