Global Variome shared LOVD

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

Phenotype #0000207691 Individual ID 00269895 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Global developmental delay (HP:0001263); Seizures (HP:0001250); Visual impairment (HP:0000505); Abnormal delivery (HP:0001787) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name IMGAG Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by IMGAG Date created 2019-12-10 12:32:00 +01:00 (CET) Date last edited 2020-04-01 13:57:49 +02:00 (CEST)

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