cone-rod dystrophy 18
cone-rod dystrophy that has material basis in homozygous mutation in the RAB28 gene on chromosome 4p15
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 18
en CONE-ROD DYSTROPHY 18; CORD18
en cone-rod dystrophy type 18
en CORD18
🔖 Identifiers · 6
- Disease Ontology ID
- DOID:0111024
- Exact match
- purl.obolibrary.org, identifiers.org, www.orpha.net
- Mondo ID
- MONDO_0014153
- OMIM ID
- 615374
- UMLS CUI
- C3809299
- UniProt disease ID
- DI-03861
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Summary
cone-rod dystrophy 18 is a rare disease[1].