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Leopard Syndrome 3 (MONDO:0013380)

Any Noonan syndrome with multiple lentigines in which the cause of the disease is a mutation in the BRAF gene.

Overview

Category

Ontology ID

Internal:14413

Synonyms

BRAF Noonan syndrome with multiple lentigines

LEOPARD syndrome 3

Leopard syndrome type 3

Noonan syndrome with multiple lentigines caused by mutation in BRAF

leopard syndrome 3

LPRD3

Mapped terms

DOID:0080550

GARD:0015694

MEDGEN:462321

OMIM:613707

UMLS:C3150971

Child terms

Unknown children.