DCHS2

dachsous cadherin-related 2
OMIM: 612486, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber DCHS2 in Pituitary hormone deficiency


Version 3.12
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Expert review
Phenotypes
  • pituitary stalk interruption syndrome, MONDO:0019828
Tags
  • watchlist
Red DCHS2 in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.544
Latest signed off version: v5.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    Phenotypes
    • pituitary stalk interruption syndrome, MONDO:0019828