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Autosomal dominant childhood-onset cortical cataract
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
B-cell chronic lymphocytic leukemia
Dyskeratosis congenita
Hoyeraal-Hreidarsson syndrome
Retinopathy - anemia- central nervous system anomalies
Synonym(s):
- Autosomal dominant childhood-onset progressive cortical cataract
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: no data available
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
CRYGS P22914123730
No signs/symptoms info available.