Search Ontology: 
        
        Human Disease
            immunodeficiency 49
- Term ID
 - DOID:0111979
 - Synonyms
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- IMD49
 - SCID, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities
 - severe combined immunodeficiency 49
 - severe combined immunodeficiency, T-cell negative, B-cell positive, NK cell positive, with intellectual disability, spasticity, and craniofacial abnormalities
 
 - Definition
 - A T cell deficiency characterized by T cell lymphopenia, low T-cell receptor excision circles, impaired T-cell proliferative responses, dysmorphic facial features, hypotonia and severe global developmental delay that has_material_basis_in heterozygous mutation in the BCL11B gene on chromosome 14q32.2. (2)
 - References
 - 
    
        
        
    
    
- MIM:617237
 - UMLS_CUI:C4310656
 
 - Ontology
 - Human Disease ( DOID:0111979 )
 
                
                    
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                        Zebrafish Models