FGF13

fibroblast growth factor 13
OMIM: 300070, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green FGF13 in Mendeliome


Version 1.1902

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Developmental and epileptic encephalopathy 90, MIM# 301058
  • Intellectual developmental disorder, X-linked 110, MIM# 301095
Tags
  • 5'UTR

Green FGF13 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Developmental and epileptic encephalopathy 90, MIM# 301058
    • Intellectual disability
    • epilepsy

    Green FGF13 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Developmental and epileptic encephalopathy 90, MIM# 301058
    • Intellectual developmental disorder, X-linked 110, MIM# 301095
    Tags
    • 5'UTR