Global Variome shared LOVD

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Phenotype #0000313564 Individual ID 00422350 Associated disease - Phenotype details family history of retinal disease: father, brother; family history of microcephaly: brother; head circumference2nd percentile (37.1 cm at 2m); age at first visit (years): 0.2age at last visit (years): –; follow up (years): 0; birth weight (kg): not available; intellectual disability: ; epilepsy: no; growth retardation: no; lymphedema: yes; additional symptoms: none report Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite familial exudative vitreoretinopathy Age/Examination - 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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