Global Variome shared LOVD

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Phenotype #0000313563 Individual ID 00422349 Associated disease - Phenotype details family history of retinal disease: father, brother; family history of microcephaly: brother; head circumference<1st percentile (38 cm at 4m); age at first visit (years): 0.3age at last visit (years): 1.1; follow up (years): 0.8; birth weight (kg): 3.49; intellectual disability: ; epilepsy: no; growth retardation: no; lymphedema: yes; additional symptoms: none reported Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite familial exudative vitreoretinopathy 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 International Created by Anna Tracewska Date created 2022-11-09 18:36:37 +01:00 (CET) Date last edited N/A

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