Disease #00045 (PJS (PEUTZ-JEGHERS SYNDROME), OMIM:175200)

Official abbreviation PJS
Name PEUTZ-JEGHERS SYNDROME
OMIM ID 175200
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene STK11
Associated tissues -
Disease features -
Remarks -

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