Global Variome shared LOVD

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

Phenotype #0000332029 Individual ID 00442682 Associated disease NMD Diagnosis/Initial Slow fetal movements, polyhydramnion, arthrogryposis Diagnosis/Definite - Phenotype details deceased; arthrogryposis multiplex; muscle biopsy: no specific changes; prenatal ultrasound: lack of fetal movement; Inheritance Familial, autosomal recessive Age/Examination <0d Age/Diagnosis - Age/Onset <0d 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 2023-11-23 18:48:51 +01:00 (CET) Date last edited N/A

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