Disease #05768 (CVDP1 (dysplasia, valvular, cardiac, type 1), OMIM:212093)

Official abbreviation CVDP1
Name dysplasia, valvular, cardiac, type 1
OMIM ID 212093
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PLD1
Associated tissues -
Disease features -
Remarks -
Date created 2020-06-11 15:04:05 +02:00 (CEST)
Date last edited 2024-01-26 11:42:20 +01:00 (CET)


Individuals

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00447729 283496 - prenatal trio exom after ultrasound abnormalities; family, 2 affected F yes Saudi Arabia - - - - - CVDP1 Abnormality of prenatal development or birth, Abnormal fetal cardiovascular morphology, Biparietal narrowing, Muscular ventricular septal defect, Endocardial fibroelastosis, Coronary cameral fistula to right ventricle PLD1 PLD1 1 2 Andreas Laner
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