cone-rod dystrophy 9
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the ADAM9 gene on chromosome 8p11
Facts
4 properties- Instance of
- rare disease, class of disease[2]
- Subclass of
- cone-rod dystrophy[3]
- On focus list of Wikimedia project
- WikiProject Medicine[5]
🏷️ Also known as
en cone-rod dystrophy 9
en CONE-ROD DYSTROPHY 9; CORD9
en Cone-Rod Dystrophy type 9
en CORD9
es distrofia de conos y bastones 9
🔖 Identifiers · 6
- Disease Ontology ID
- DOID:0111020
- Exact match
- purl.obolibrary.org, identifiers.org
- Mondo ID
- MONDO_0013002
- OMIM ID
- 612775
- UMLS CUI
- C1423873
- UniProt disease ID
- DI-02490
Press Enter · cited answer in seconds
0 sources
Summary
cone-rod dystrophy 9 is a rare disease[1].