cone-rod dystrophy 10
cone-rod dystrophy that has material basis in compound heterozygous mutation in the SEMA4A gene on chromosome 1q22
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 10
en CONE-ROD DYSTROPHY 10; CORD10
en cone-rod dystrophy type 10
en CORD10
🔖 Identifiers · 7
- Disease Ontology ID
- DOID:0111017
- Exact match
- purl.obolibrary.org, identifiers.org, www.orpha.net
- MeSH descriptor ID
- C564597
- Mondo ID
- MONDO_0012464
- UMLS CUI
- C1846529
- UniProt disease ID
- DI-00324
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Summary
cone-rod dystrophy 10 is a rare disease[1].