Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000143183 Individual ID 00180919 Associated disease OPA Phenotype details Behavioral abnormality (HP:0000708), Obesity (HP:0001513), Microcephaly (HP:0000252) Diagnosis/Initial optic atrophy Inheritance Familial, autosomal dominant Diagnosis/Definite OPA-1 Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Birth_Details - MotorSkills - Vision/Abnormality nr Hearing/Loss nr Eye/Optic_Disc - Protein - Brain/Imaging - Eye/OCT - Vision/Field - Vision/Acuity - Vision/Colour - Habits - Owner name Thomas Foulonneau Database submission license No license selected Created by Thomas Foulonneau Date created 2018-09-11 10:42:44 +02:00 (CEST) Date last edited 2018-11-16 15:42:11 +01:00 (CET)

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