GON4L

gon-4 like
OMIM: 610393, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green GON4L in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.10
Latest signed off version: v7.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Li-Takada-Miyake syndrome, OMIM:621212
  • Li-Takada-Miyake syndrome, MONDO:0978303
Red GON4L in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • AUTOSOMAL RECESSIVE MENTAL RETARDATION
    • Li-Takada-Miyake syndrome, OMIM:621212
    • Li-Takada-Miyake syndrome, MONDO:0978303
    Amber GON4L in Intellectual disability


    Level 2: Developmental disorders
    Version 10.17
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    Phenotypes
    • Li-Takada-Miyake syndrome, OMIM:621212
    • Li-Takada-Miyake syndrome, MONDO:0978303