Global Variome shared LOVD

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

Phenotype #0000268965 Individual ID 00373741 Associated disease OCCM Phenotype details HP:0001263; HP:0001999; HP:0001249; HP:0002098; HP:0001252; HP:0000954; HP:0001655; HP:0008081; HP:0000316 Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite Cortical malformations, occipital (OMIM 614115) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Wenjuan Qiu Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Wenjuan Qiu Date created 2021-05-19 16:58:54 +02:00 (CEST) Date last edited 2021-05-28 12:07:25 +02:00 (CEST)

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