Phenotype #0000278958

Individual ID 00385162
Associated disease -
Phenotype details HP:0007973:Retinal dysplasia; HP:0000541:Retinal detachment; (Bilateral vitreo-retinal dysplasia); HP:0000618:Blindness; HP:0000407:Sensorineural hearing impairment; HP:0001250:Seizures; HP:0000718:Aggressive behaviour
Diagnosis/Initial FEVR
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 1y1m (1 year, 1 month)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2021-10-08 17:29:22 +02:00 (CEST)
Date last edited N/A

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