cataract 10 multiple types
cataract that has material basis in heterozygous mutation in the CRYBA1 gene on chromosome 17q11
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 10 multiple types
en CATARACT 10, MULTIPLE TYPES
en CATARACT 10, MULTIPLE TYPES; CTRCT10
en Cataract, Congenital Zonular, With Sutural Opacities
en CCZS
en congenital zonular cataract with sutural opacities
en CTRCT10
🔖 Identifiers · 8
- Disease Ontology ID
- DOID:0110258
- Exact match
- purl.obolibrary.org, identifiers.org
- ICD-10-CM
- Q12.0
- MeSH descriptor ID
- C563435
- Mondo ID
- MONDO_0010948
- OMIM ID
- 600881
- UMLS CUI
- C1833229
- UniProt disease ID
- DI-01423
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Summary
cataract 10 multiple types is a rare disease[1].