Disease association ontology term - MONDO:0011338 - Omenn syndrome
Term summary
- ID
- MONDO:0011338
- Name
- Omenn syndrome
- Ontology or CV name
- Disease association
- Definition
- An inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID).
