Global Variome shared LOVD

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

Phenotype #0000207960 Individual ID 00271353 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details Congenital microcephaly (HP:0011451); Global developmental delay (HP:0001263); Abnormal cortical gyration (HP:0002536); Epicanthus (HP:0000286); Clinodactyly of the 5th finger (HP:0004209); Strabismus (HP:0000486) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2019-12-18 16:25:33 +01:00 (CET) Date last edited 2020-04-02 12:33:15 +02:00 (CEST)

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