GGPS1

geranylgeranyl diphosphate synthase 1
OMIM: 606982, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green GGPS1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome, MIM# 619518
  • Muscular dystrophy
  • Deafness
  • Ovarian insufficiency

Green GGPS1 in Muscular dystrophy and myopathy_Paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Expert Review Green
    • Literature
    Phenotypes
    • Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome, MIM# 619518
    • Muscular dystrophy
    • Deafness
    • Ovarian insufficiency

    Green GGPS1 in Deafness_IsolatedAndComplex


    Level 2: Hearing and ear disorders
    Version 1.194

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome, MIM# 619518
    • Muscular dystrophy
    • Deafness
    • Ovarian insufficiency

    Green GGPS1 in Primary Ovarian Insufficiency_Premature Ovarian Failure

    Level 3: Gonadal and sex development disorders
    Level 2: Endocrine disorders
    Version 0.328

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Expert Review Green
    • Literature
    Phenotypes
    • Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome, MIM# 619518
    • Muscular dystrophy
    • deafness
    • ovarian insufficiency