Phenotype #0000280198

Individual ID 00386391
Associated disease MCAHS1;GPIBD3
Phenotype details Omphalocele, Hydronephrosis, Echogenic fetal bowel, Increased nuchal translucency, Dextrocardia, Abnormality of ductus venosus blood flow
Diagnosis/Initial prenatal ultrsound
Inheritance Familial, autosomal recessive
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 2021-10-22 13:24:54 +02:00 (CEST)
Date last edited 2021-10-22 14:32:47 +02:00 (CEST)

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