Global Variome shared LOVD

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

Phenotype #0000155626 Individual ID 00207842 Associated disease MOPD Diagnosis/Initial MOPD Diagnosis/Definite MOPD-1 Phenotype details microcephaly (HP:0000252); typical face; musculoskeletal features; no other organ anomalies; skin/hair features Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2018-12-02 14:22:28 +01:00 (CET) Date last edited N/A

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