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Disease

Apert syndrome

Also known as ACS1, acrocephalosyndactyly type 1, acrocephalosyndactyly type I, type I Acrocephalosyndactyly+8 more

ACS1, acrocephalosyndactyly type 1, acrocephalosyndactyly type I, type I Acrocephalosyndactyly, ACS 1, ACS 2, Apert-Crouzon disease, Vogt Cephalodactyly, acrocephalo-syndactyly type 1, acrocephalosyndactyly, type 1, acrocephalosyndactyly, type 2, syndactylic oxycephaly.

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.

FGFR20.83

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.

Fibroblast growth factor receptor 2via FGFR20.83

Reference

Authoritative identity, definition & identifiers.

Synonyms

ACS1, acrocephalosyndactyly type 1, acrocephalosyndactyly type I, type I Acrocephalosyndactyly, ACS 1, ACS 2, Apert-Crouzon disease, Vogt Cephalodactyly, acrocephalo-syndactyly type 1, acrocephalosyndactyly, type 1, acrocephalosyndactyly, type 2, syndactylic oxycephaly

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.