cataract 15 multiple types
cataract that has material basis in heterozygous mutation in the MIP gene on chromosome 12q13
Facts
5 properties- Instance of
- rare disease, class of disease[2]
- Subclass of
- cataract, autosomal dominant disease[3][4]
- Health specialty
- medical genetics[5]
- On focus list of Wikimedia project
- WikiProject Medicine[7]
🏷️ Also known as
en cataract 15 multiple types
en CATARACT 15, MULTIPLE TYPES
en CATARACT 15, MULTIPLE TYPES; CTRCT15
en CTRCT15
🔖 Identifiers · 8
- Disease Ontology ID
- DOID:0110251
- Exact match
- purl.obolibrary.org, identifiers.org
- ICD-10-CM
- Q12.0
- Mondo ID
- MONDO_0014110
- OMIM ID
- 615274
- Orphanet ID
- 217052
- UMLS CUI
- C3809001
- UniProt disease ID
- DI-03782
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Summary
cataract 15 multiple types is a rare disease[1].