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Disease

LEOPARD syndrome 3

Also known as BRAF Noonan syndrome with multiple lentigines, Leopard syndrome type 3, Noonan syndrome with multiple lentigines caused by mutation in BRAF, LPRD3.

1
Associated genes
1
Related proteins

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Associated genes

1 match

Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.

BRAF0.76

Disease biology

1 match

Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.

Serine/threonine-protein kinase B-rafvia BRAF0.76

Reference

Authoritative identity, definition & identifiers.

Synonyms

BRAF Noonan syndrome with multiple lentigines, Leopard syndrome type 3, Noonan syndrome with multiple lentigines caused by mutation in BRAF, LPRD3

References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.