Disease #00162 (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 2023-06-27 12:13:13 +00:00 (UTC)
Date last edited N/A

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