Phenotype #0000245862

Individual ID 00327616
Associated disease neuropathy, optic
Phenotype details Very low visual acuity (HP:0032122); Optic atrophy (HP:0000648);
Optic neuropathy (HP:0001138);
Diagnosis/Initial -
Diagnosis/Definite -
Inheritance Familial, autosomal recessive
Age/Examination <16y (before 16 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Aude Rocatcher
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Aude Rocatcher
Date created 2021-01-25 10:18:22 +01:00 (CET)
Date last edited 2021-01-27 19:07:15 +01:00 (CET)

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