Global Variome shared LOVD

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

Phenotype #0000324780 Individual ID 00434444 Associated disease GRBGD Phenotype details Abnormality of prenatal development or birth, Skeletal dysplasia, Thickened nuchal skin fold, Micromelia, Postaxial polydactyly, Abnormal thorax morphology, Single umbilical artery Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 13+5 Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2023-03-31 13:20:55 +02:00 (CEST) Date last edited 2023-03-31 16:09:14 +02:00 (CEST)

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