LAMC3

laminin subunit gamma 3
OMIM: 604349, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels
Red LAMC3 in Cerebral vascular malformations


Level 2: Neurology
Version 5.3
Latest signed off version: v5.2 (12 Aug 2026)

review Not set
Sources
  • Yorkshire and North East GLH
  • NHS GMS
  • Expert Review Red
  • UKGTN
Phenotypes
  • Cerebral Malformation Disorders
Green LAMC3 in Malformations of cortical development


Level 2: Neurology
Version 8.11
Latest signed off version: v8.6 (12 Aug 2026)

Component of the following Super Panels:

  • Cerebral malformation
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Radboud University Medical Center, Nijmegen
    • UKGTN
    • Emory Genetics Laboratory
    • Other
    Phenotypes
    • Cortical malformations, occipital, OMIM:614115
    • occipital pachygyria and polymicrogyria, MONDO:0013583
    Green LAMC3 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 8.7
    Latest signed off version: v8.0 (12 Aug 2026)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • PAGE DD-Gene2Phenotype
    Phenotypes
    • Cortical malformations, occipital, OMIM:614115
    • occipital pachygyria and polymicrogyria, MONDO:0013583
    Green LAMC3 in DDG2P


    Version 8.2
    Latest signed off version: v8.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • OCCIPITAL CORTICAL MALFORMATIONS 614115
    Green LAMC3 in Early onset or syndromic epilepsy


    Level 2: Neurology
    Version 9.84
    Latest signed off version: v9.56 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Cortical malformations, occipital, OMIM:614115
    • occipital pachygyria and polymicrogyria, MONDO:0013583
    Red LAMC3 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.31
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • NHS GMS
    • Victorian Clinical Genetics Services
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • Cortical malformations, occipital, OMIM:614115
    • occipital pachygyria and polymicrogyria, MONDO:0013583