cataract 9 multiple types
Information
- Disease name
- cataract 9 multiple types
- Disease ID
- DOID:0110266
- Description
- "A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22." [url:https\://www.ncbi.nlm.nih.gov/pubmed/26867756, url:https\://www.omim.org/entry/604219]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:83
- Cross Reference ID (Disease Ontology)
- ICD10CM:Q12.0
- Cross Reference ID (Disease Ontology)
- MIM:604219
- Exact Synonym (Disease Ontology)
- cataract 9 multiple types with or without microcornea
- Exact Synonym (Disease Ontology)
- CTRCT9
- Disase Synonym (Disease Ontology)
- autosomal recessive congenital cataract 1
- Disase Synonym (Disease Ontology)
- CATC1