Global Variome shared LOVD

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

Phenotype #0000157523 Individual ID 00208915 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details HP:0002104 (Apnea); HP:0002804 (Arthrogryposis multiplex congenita); HP:0000035 (Abnormality of the testis); HP:0000486 (Strabismus); HP:0001655 (Patent foramen ovale); HP:0000278 (Retrognathia); HP:0011025 (Abnormality of cardiovascular system physiology); HP:0001252 (Muscular hypotonia); HP:0012758 (Neurodevelopmental delay) 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 2018-12-20 13:06:26 +01:00 (CET) Date last edited 2019-02-24 22:35:08 +01:00 (CET)

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