PanelApp (staging)
  1. Genes and Genomic Entities
  2. PDCD10

PDCD10

programmed cell death 10
OMIM: 609118, ClinGen, DECIPHER

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green PDCD10 in Mendeliome


Version 1.2302

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Cerebral cavernous malformations 3 MIM#603285

Green PDCD10 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.108

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Cerebral cavernous malformations-3 MIM#603285

    Amber PDCD10 in Vascular Malformations_Germline


    Level 2: Cardiovascular disorders
    Version 1.12

    Component of the following Super Panels:

  • Vascular Malformations SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Royal Melbourne Hospital
    Phenotypes
    • Cerebral cavernous malformations 3

    Green PDCD10 in Stroke


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.16

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Cerebral cavernous malformations 3 MIM#603285

    Green PDCD10 in Cerebral vascular malformations


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.0

    Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Genomics England PanelApp
    • Expert Review Green
    Phenotypes
    • Cerebral Cavernous Malformations
    • Cerebral cavernous malformations 3
    • Cerebral cavernous malformations 3, 603285
    • Cerebral Cavernous Malformation
    • Familial Cerebral Cavernous Malformation

    Green PDCD10 in Fetal anomalies


    Version 1.313

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Cerebral cavernous malformations 3 MIM#603285