Phenotype #0000303337

Individual ID 00411261
Associated disease ASGD1
Phenotype details Visual impairment, Abnormal eye morphology, Congenital primary aphakia
Diagnosis/Initial 1y
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2022-06-09 11:41:19 +02:00 (CEST)
Date last edited 2022-11-14 15:33:45 +01:00 (CET)

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