Omenn syndrome
https://rarediseases.info.nih.gov/diseases/8198/omenn-syndrome
An inflammatory condition characterized by erythroderma, desquamation, alopecia, chronic diarrhea, failure to thrive, lymphadenopathy, and hepatosplenomegaly, associated with severe combined immunodeficiency (SCID).
MedDRA:10069097
severe combined immunodeficiency with hypereosinophilia
OMIM:603554
UMLS:C2700553
MONDO:0011338
SCTID:722067005
NCIT:C61240
reticuloendotheliosis familial with eosinophilia
Orphanet:39041
reticuloendotheliosis, familial, with eosinophilia
DOID:0060010
Omenn syndrome
combined immunodeficiency with hypereosinophilia
GARD:8198
T-B- severe combined immunodeficiency
non-SCID combined immunodeficiency
familial severe combined immunodeficiency