Global Variome shared LOVD

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

Phenotype #0000203111 Individual ID 00265313 Associated disease PHPVAR Phenotype details persistent hyperplasia of the primary vitreous (PHPV, HP:0007968), gross nystagmus (HP:0000639) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite congenital nonsyndromic persistent hyperplasia of the primary vitreous Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Jasmine Chen Database submission license No license selected Created by Jasmine Chen Date created 2019-09-19 21:31:40 +02:00 (CEST) Date last edited 2019-09-27 13:50:10 +02:00 (CEST)

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