Global Variome shared LOVD
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Phenotype #0000308489
Individual ID
00416979
Associated disease
NS3
Phenotype details
Hydronephrosis, Single umbilical artery, Abnormality of prenatal development or birth, Intrauterine growth retardation, Hydrops fetalis, Fetal ascites, Atrioventricular canal defect, Fetal cystic hygroma, Fetal pyelectasis, Fetal hydrothorax
Diagnosis/Initial
prenatal
Inheritance
Isolated (sporadic)
Diagnosis/Definite
-
Age/Examination
-
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
2022-09-12 11:38:44 +02:00 (CEST)
Date last edited
2022-09-12 16:14:52 +02:00 (CEST)
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