SOS1-related bone marrow dysplasia*

Back to search Result
WHO-ICD-10 version:2010

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Haemolytic anaemias

Mode of Inheritance

Autosomal Dominant

Gene Map Locus



Heterozygous mutation in SOS1 was associated with bone marrow dysplasia and anemia in a patient [From PMID:31130284]

Epidemiology in the Arab World

View Map
Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
SOS1.1United Arab EmiratesMaleNo Anemia; MyelodysplasiaNM_005633.3:c.1297G>AHeterozygousAutosomal, DominantMonies et al. 2019 Previously unreporte...
© CAGS 2024. All rights reserved.