cerebral palsy
MONDO:0006497Mondo
Findings
No curated finding names cerebral palsy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
A group of disorders affecting the development of movement and posture, often accompanied by disturbances of sensation, perception, cognition, and behavior. It results from damage to the fetal or infant brain.
Definition from the Mondo Disease Ontology (MONDO:0006497), read 2026-09-29. CC BY 4.0.
Genes
8 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- FBXO31HGNC:16510
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Limited · Ambry Genetics · Autosomal dominant · 2025
- AGAP1HGNC:16922
- Moderate · PanelApp Australia · Autosomal dominant · 2025
- RHOBHGNC:668
- Moderate · PanelApp Australia · Autosomal dominant · 2025
- TEP1HGNC:11726
- Moderate · PanelApp Australia · Autosomal dominant · 2025
- KDM7AHGNC:22224
- Limited · PanelApp Australia · Autosomal dominant · 2025
- MAOBHGNC:6834
- Limited · PanelApp Australia · Autosomal dominant · 2025
- RFX2HGNC:9983
- Limited · Ambry Genetics · Autosomal dominant · 2018
- TENM1HGNC:8117
- Limited · Ambry Genetics · X-linked · 2018
Where it sits
- A kind of
Other names
1 name
Resolves to: cerebral palsy
- Also called
- infantile cerebral palsy