cone-rod dystrophy 9
MONDO:0013002Mondo
Findings
No curated finding names cone-rod dystrophy 9 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any cone-rod dystrophy in which the cause of the disease is a mutation in the ADAM9 gene.
Definition from the Mondo Disease Ontology (MONDO:0013002), 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.
- ADAM9HGNC:216
- Definitive · Illumina · Autosomal recessive · 2021
- Definitive · G2P · Autosomal recessive · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2018
Where it sits
Other names
4 names
Resolves to: cone-rod dystrophy 9
- Also called
- ADAM9 cone-rod dystrophycone-rod dystrophy caused by mutation in ADAM9cone-rod dystrophy type 9CORD9