Phenotype #0000313565

Individual ID 00422351
Associated disease -
Phenotype details family history of retinal disease: none; family history of microcephaly: none; head circumferencenot available; age at first visit (years): 3age at last visit (years): 29; follow up (years): 26; birth weight (kg): not available; intellectual disability: ; epilepsy: no; growth retardation: no; lymphedema: no; additional symptoms: none reported
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite familial exudative vitreoretinopathy
Age/Examination 29y (29 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-11-09 18:36:37 +01:00 (CET)
Date last edited N/A

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