Global Variome shared LOVD

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

Phenotype #0000155494 Individual ID 00207703 Associated disease STL4 Phenotype details Congenital sensorineural hearing loss High myopia Hypoplastic vitreous Flat midface Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Stickler Syndrome Age/Examination 02y (2 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Thomas Nixon Database submission license No license selected Created by Thomas Nixon Date created 2018-11-28 23:59:05 +01:00 (CET) Date last edited 2018-12-07 19:23:47 +01:00 (CET)

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