MSN

moesin
OMIM: 309845, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green MSN in COVID-19 research


Level 2: Viral research
Version 1.142

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Expert list
  • NHS GMS
  • North West GLH
  • London North GLH
  • IUIS Classification February 2018
  • Expert Review Green
  • ESID Registry 20171117
Phenotypes
  • Combined immunodeficiency
  • Immunodeficiency 50, MIM300988
  • Immunodeficiency 50, 300988
  • Immunodeficiencies affecting cellular and humoral immunity
  • Recurrent infections with bacteria, varicella, neutropenia
Green MSN in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 4.202
Latest signed off version: v4.0 (22 Mar 2023)

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Other
  • NHS GMS
  • North West GLH
  • London North GLH
  • IUIS Classification February 2018
  • ESID Registry 20171117
Phenotypes
  • Combined immunodeficiency
  • Immunodeficiency 50, 300988
  • Recurrent infections with bacteria, varicella, neutropenia
  • Immunodeficiencies affecting cellular and humoral immunity
Red MSN in Cytopenia - NOT Fanconi anaemia


Version 3.34
Latest signed off version: v3.0 (22 Mar 2023)

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Expert review Red
  • NHS GMS
  • North West GLH
  • London South GLH
  • Yorkshire and North East GLH
  • Wessex and West Midlands GLH
Phenotypes
  • Immunodeficiency 50, 300988
Green MSN in Severe Paediatric Disorders


Version 1.184

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Next Generation Children Project
  • Expert Review Green
  • Expert list
Phenotypes
  • Immunodeficiency 50, 300988