Disease #00151 (JPS (JUVENILE POLYPOSIS SYNDROME), OMIM:174900)

Official abbreviation JPS
Name JUVENILE POLYPOSIS SYNDROME
OMIM ID 174900
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SMAD4
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-27 09:06:44 +00:00 (UTC)
Date last edited N/A