Global Variome shared LOVD

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

Phenotype #0000171839 Individual ID 00227817 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details HP:0001392 (Abnormality of the liver) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Gunnar Schmidt Database submission license Creative Commons Attribution 4.0 International Created by Gunnar Schmidt Date created 2019-03-12 18:22:07 +01:00 (CET) Date last edited 2019-03-13 12:15:54 +01:00 (CET)

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