Disease #00021 (LFS1 (LI-FRAUMENI SYNDROME 1), OMIM:151623)

Official abbreviation LFS1
Name LI-FRAUMENI SYNDROME 1
OMIM ID 151623
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TP53
Associated tissues -
Disease features -
Remarks -

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