Global Variome shared LOVD

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

Phenotype #0000313567 Individual ID 00422353 Associated disease - Phenotype details family history of retinal disease: daughter; family history of microcephaly: daughter; head circumference<1st percentile (48.5 cm at 11y); age at first visit (years): 11age at last visit (years): 24; follow up (years): 13; birth weight (kg): 2.8; intellectual disability: ; epilepsy: no; growth retardation: no; lymphedema: not available; additional symptoms: none reported Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite familial exudative vitreoretinopathy Age/Examination 24y (24 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

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.