Lymphatic malformation 1
Also known as FLT4 hereditary lymphedema, LMPH1A, Milroy disease, Nonne-Milroy disease+13 more
FLT4 hereditary lymphedema, LMPH1A, Milroy disease, Nonne-Milroy disease, Nonne-Milroy lymphedema, Nonne-Milroy syndrome, Nonne’s syndrome, congenital hereditary lymphedema, congenital primary lymphedema, early onset lymphedema, hereditary lymphedema 1, hereditary lymphedema caused by mutation in FLT4, hereditary lymphedema type I, lymphedema, early-onset, lymphedema, hereditary, 1A, lymphedema, hereditary, type 1A, primary congenital lymphedema.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
FLT4 hereditary lymphedema, LMPH1A, Milroy disease, Nonne-Milroy disease, Nonne-Milroy lymphedema, Nonne-Milroy syndrome, Nonne’s syndrome, congenital hereditary lymphedema, congenital primary lymphedema, early onset lymphedema, hereditary lymphedema 1, hereditary lymphedema caused by mutation in FLT4, hereditary lymphedema type I, lymphedema, early-onset, lymphedema, hereditary, 1A, lymphedema, hereditary, type 1A, primary congenital lymphedema
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.