Disease #06044 (PVNH8 (heterotopia, nodular, periventricular, type 8), OMIM:618185)

Official abbreviation PVNH8
Name heterotopia, nodular, periventricular, type 8
OMIM ID 618185
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ARF1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2024-04-19 19:01:34 +02:00 (CEST)


Individuals

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00416550 205242 - prenatal trio Dx after ultrasound abnormalities M no - - - - - - PVNH8 Hydrops fetalis, Fetal akinesia sequence, Elbow flexion contracture, Knee flexion contracture, Talipes equinovarus, Scoliosis ARF1 ARF1 1 1 Andreas Laner
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