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Disease association ontology term - MONDO:0009973 - reticular dysgenesis

Term summary

ID
MONDO:0009973
Name
reticular dysgenesis
Ontology or CV name
Disease association
Definition
Reticular dysgenesis is the most severe form of severe combined immunodeficiency (SCID) and is characterized by bilateral sensorineural deafness and a lack of innate and adaptive immune functions leading to fatal septicemia within days after birth if not treated.

Parents

Annotation

Disease association

MONDO:0009973 - reticular dysgenesis

References:

Genes: