Phenotype #0000155299

Individual ID 00207521
Associated disease BVVLS-1
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