Autosomal dominant vitreoretinochoroidopathy

Preferred Label : Autosomal dominant vitreoretinochoroidopathy;

ICD-11 definition : Autosomal dominant vitreoretinochoroidopathy is a genetic vitreous-retinal disease characterized by ocular developmental anomalies such as microcornea, a shallow anterior chamber, glaucoma and cataract. There is abnormal chorioretinal pigmentation, usually lying between the vortex veins and the ora serrata for 360 degrees.;

Details

Origin ID

96951767;

Currated CISMeF NLP mapping
- Autosomal dominant vitreoretinochoroidopathy [ORDO Disease]
- Autosomal dominant vitreoretinochoroidopathy (disorder) [SNOMED CT concept]
- Vitreoretinochoroidopathy [OMIM Phenotype]
- autosomal dominant vitreoretinochoroidopathy [DO Concept]
- vitreoretinochoroidopathy [MeSH Supplementary Concept]

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