Global Variome shared LOVD

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

Phenotype #0000086063 Individual ID 00108467 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Congenital glaucoma Axenfeld-Rieger anomaly myopia sensorineural hearing loss congenital hypothyroidism arterial tortuosity microcephaly delayed eruption of permanent teeth femoral retroversion Inheritance Familial, autosomal dominant Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Elena Semina Database submission license No license selected Created by Elena Semina Date created 2017-07-24 23:43:06 +02:00 (CEST) Date last edited 2017-07-29 21:42:29 +02:00 (CEST)

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