Global Variome shared LOVD

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

Phenotype #0000115936 Individual ID 00143186 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details microcephaly (HP:0000252), cortical atrophy (HP:?), hypofibrinogenemia (HP:0011900) Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name N/A Database submission license No license selected Created by Johan den Dunnen Date created 2017-11-29 07:40:43 +01:00 (CET) Date last edited N/A

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