Global Variome shared LOVD

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

Phenotype #0000143352 Individual ID 00181106 Associated disease Apert Phenotype details Corpus callosum agenesis, small brain, mesocardia, syndactylies on hand and feet Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite Apert syndrome Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Isabel Filges Database submission license No license selected Created by Isabel Filges Date created 2018-09-28 13:41:16 +02:00 (CEST) Date last edited 2018-10-09 19:59:01 +02:00 (CEST)

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