Disease #00165 (LPRD3 (LEOPARD SYNDROME 3), OMIM:613707)

Official abbreviation LPRD3
Name LEOPARD SYNDROME 3
OMIM ID 613707
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BRAF
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-27 12:56:54 +00:00 (UTC)
Date last edited N/A

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