Disease #00642 (LPRD3 (LEOPARD syndrome, type 3 (LPRD-3)), OMIM:613707)

Official abbreviation LPRD3
Name LEOPARD syndrome, type 3 (LPRD-3)
OMIM ID 613707
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene BRAF
Associated tissues -
Disease features -
Remarks -

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