IMPG1-related recessive retinopathy
MONDO:1040037Mondo
Findings
No curated finding names IMPG1-related recessive retinopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any retinopathy caused by autosomal recessive variants in the IMPG1 gene.
Definition from the Mondo Disease Ontology (MONDO:1040037), read 2026-09-29. CC BY 4.0.
Genes
1 gene
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.
- HGNC:6055HGNC:6055
- Definitive · ClinGen · Autosomal recessive · 2023
Where it sits
- Narrower terms (1)