TNR

tenascin R
OMIM: 601995, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber TNR in Childhood onset hereditary spastic paraplegia


Level 2: Neurology
Version 8.30
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus, OMIM:619653
Tags
  • Q3_25_promote_green
Amber TNR in Intellectual disability


Level 2: Developmental disorders
Version 9.279
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus, OMIM:619653
    Tags
    • Q3_25_promote_green
    Amber TNR in Childhood onset dystonia, chorea or related movement disorder


    Level 2: Neurology
    Version 7.13
    Latest signed off version: v7.0 (30 Apr 2025)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus, OMIM:619653
    Tags
    • Q3_25_promote_green