Phenotype #0000039145

Individual ID 00052568
Associated disease LCA
Phenotype details Leber congenital amaurosis; congenital blindness, reduced or non detectable ERG, oculodigital sign, refractive errors, photosensitivity
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Muhammad Ajmal
Database submission license No license selected
Created by Muhammad Ajmal