Global Variome shared LOVD

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Phenotype #0000210218 Individual ID 00275607 Associated disease ? Diagnosis/Initial multiple organ defects Diagnosis/Definite VCRL3 Phenotype details see paper; ..., left renal and ureter agenesis; micromelia, bilateral club feet; hydrocephalus, small thorax, echogenic bowel, flat nose and low set ears, edema, polysplenia, pulmonary hypoplasia Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2020-01-11 09:04:48 +01:00 (CET) Date last edited 2020-12-02 09:40:55 +01:00 (CET)

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