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Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant (DOID:9004785)
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Parent Terms Term With Siblings Child Terms
agammaglobulinemia +     
Achondroplasia and Swiss Type Agammaglobulinemia 
adenosine deaminase deficiency  
Agammaglobulinemia 1, Autosomal Recessive  
Agammaglobulinemia 2, Autosomal Recessive  
Agammaglobulinemia 3, Autosomal Recessive  
agammaglobulinemia 4  
agammaglobulinemia 5  
Agammaglobulinemia 6, Autosomal Recessive  
Agammaglobulinemia 7, Autosomal Recessive  
Agammaglobulinemia 8, Autosomal Dominant  
Agammaglobulinemia, Microcephaly, and Severe Dermatitis 
Agammaglobulinemia, non-Bruton type  
Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant 
Agammaglobulinemia, X-Linked, Type 2  
autosomal recessive osteopetrosis 7  
common variable immunodeficiency +   
Frenkel Russe Syndrome 
Good syndrome 
Granulocytopenia with Immunoglobulin Abnormality 
Hypogammaglobulinemia, X-Linked  
isolated growth hormone deficiency type III  
Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinemia 
Microcephaly with Chemotactic Defect and Transient Hypogammaglobulinemia 
Say Barber Miller Syndrome 
transient hypogammaglobulinemia +  
X-linked agammaglobulinemia  

Primary IDs: MESH:C563305 ;   RDO:0012602

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.