1. Panels
  2. Neonatal or paediatric intensive care admission with a likely monogenic cause
This Panel is marked as Internal

Neonatal or paediatric intensive care admission with a likely monogenic cause (Version 0.5)

Level 3: Multi-system groups
Level 2: Ultra-rare disorders

Relevant disorders: Neonatal or paediatric intensive care admission with a likely monogenic disease
Panel types: Rare Disease 100K
Previous code: 5763f4f18f620350a1996051
Description
This is a place-holder for a panel in progress. Please contact [email protected] if you have a relevant gene list that should be added.
Panel Activity

1 reviewer

  • Rebecca Foulger (Genomics England curator)

    Group: Other
    Workplace: Other

1 Entities

1 reviewed, 0 green

List Entity Reviews Mode of inheritance Details
1 Entities
Red List (low evidence)
USP18
1 review
 BIALLELIC, autosomal or pseudoautosomal
Sources
  • Other
Phenotypes
  • Pseudo-TORCH syndrome 2, 617397
Tags

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  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

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