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Human Disease

infantile onset multisystem autoimmune disease 3

Term ID
DOID:0061162
Synonyms
Definition
An infantile onset multisystem autoimmune disease characterized by the onset of various systemic autoimmune manifestations in the first months or years of life that has_material_basis_in homozygous mutation in the CBLB gene on chromosome 3q13. https://pubmed.ncbi.nlm.nih.gov/36006710/
References
Ontology
Human Disease   ( DOID:0061162 )
Relationships
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Genes Involved
Zebrafish Models