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General Information
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| Term |
Bietti crystalline corneoretinal dystrophy |
ID (Ontology) |
DOID:0050664 (Human Disease) |
| Definition |
A retinal degeneration that is characterized by crystals in the cornea, shiny deposits on the retina and progressive atrophy of the retina, choriocapillaris and choroid, has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the CYP4V2 gene on chromosome 4q35. |
| Also Known As |
"Bietti's crystalline dystrophy" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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Bietti crystalline corneoretinal dystrophy | 27 | for disease ribbon | Bietti crystalline corneoretinal dystrophy | 27 | model of | Bietti crystalline corneoretinal dystrophy | 27 |
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