Phenotype #0000244673

Individual ID 00326212
Associated disease VRJS
Phenotype details (+) Abnormality of prenatal development or birth,(+) Increased nuchal translucency,(+) Fetal ultrasound soft marker,(+) Abnormal heart morphology
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination 00y ()
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2021-01-11 11:36:37 +01:00 (CET)
Date last edited 2021-01-12 16:10:37 +01:00 (CET)

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