Global Variome shared LOVD

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

Phenotype #0000051146 Individual ID 00064997 Associated disease ASGD2 Phenotype details congenital primary aphasia, microphthalmia, sclerocornea Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Deepti Anand Database submission license No license selected Created by Johan den Dunnen Date created 2016-05-15 11:36:14 +02:00 (CEST) Date last edited N/A

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