Phenotype #0000185981

Individual ID 00246129
Associated disease AN
Phenotype details best corrected visual acuity R/L 0.1/0.1; no aniridia-related keratopathy; complete aniridia; aphakia, posterior capsule opacification; no glauvoma; macular hypoplasia uncertain (because of PCO); nystagmus; no strabismus ; no ptosis; normal psychomotor development
Diagnosis/Initial congenital aniridia
Inheritance Familial, autosomal dominant
Diagnosis/Definite AN-1
Age/Examination 35y (35 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-07-12 09:17:59 +02:00 (CEST)
Date last edited N/A

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