Phenotype #0000155299

Individual ID 00207521
Associated disease BVVLS1
Phenotype details Visual impairment (HP:0000505)
Hearing impairment (HP:0000365)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite BVVLS
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Gunnar Schmidt
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Gunnar Schmidt
Date created 2018-11-23 18:16:47 +01:00 (CET)
Date last edited 2018-11-23 19:28:06 +01:00 (CET)

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