Hypermetric saccades

6 condition reports read genes linked to this trait

Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.

• Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 8 of these genesGRM1XRCC1PRDX3ANO10GDAP2VPS13DAbout this report →
• Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 4 of these genesGRM1ITPR1TMEM240ATXN1About this report →
• Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
• Neuronal Ceroid LipofuscinosisReads 1 of these genesTPP1About this report →

Every condition report

12 genes linked to Hypermetric saccades

Changes in these genes cause rare conditions in which Hypermetric saccades is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.

How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.

Broader traits

Where this comes from

• The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
• Data release 2026.10.17-8666dff2.