Global Variome shared LOVD

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Phenotype #0000313574 Individual ID 00422360 Associated disease - Phenotype details family history of retinal disease: none; family history of microcephaly: none; head circumference<1st percentile (37 cm at 6m); age at first visit (years): 0.4age at last visit (years): 6; follow up (years): 5; birth weight (kg): 2.59; intellectual disability: ; epilepsy: no; growth retardation: no; lymphedema: no; additional symptoms: delays in gross and fine motor skills Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite familial exudative vitreoretinopathy Age/Examination 6y (6 years) 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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