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Ontology Browser

Term:
Agammaglobulinemia 8 (DOID:9008152)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
agammaglobulinemia +     
Achondroplasia and Swiss Type Agammaglobulinemia 
adenosine deaminase deficiency  
Agammaglobulinemia 1, Autosomal Recessive  
Agammaglobulinemia 10, Autosomal Dominant  
Agammaglobulinemia 2, Autosomal Recessive  
Agammaglobulinemia 3, Autosomal Recessive  
agammaglobulinemia 4  
agammaglobulinemia 5  
Agammaglobulinemia 6, Autosomal Recessive  
Agammaglobulinemia 7, Autosomal Recessive  
Agammaglobulinemia 8  
Agammaglobulinemia 9, Autosomal Recessive  
Agammaglobulinemia, Microcephaly, and Severe Dermatitis 
Agammaglobulinemia, non-Bruton type 
Agammaglobulinemia, Non-Bruton Type, Autosomal Dominant 
autosomal recessive osteopetrosis 7  
common variable immunodeficiency +   
Frenkel Russe Syndrome 
Good syndrome 
immunodeficiency 59  
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 +   
X-Linked Hypogammaglobulinemia  

Synonyms
Exact Synonyms: AGM8
Narrow Synonyms: AGM8A ;   AGM8B ;   agammaglobulinemia 8, autosomal dominant ;   agammaglobulinemia 8A, autosomal dominant ;   agammaglobulinemia 8B, autosomal recessive ;   agammaglobulinemia, autosomal dominant, due to TCF3 defect ;   agammaglobulinemia, autosomal recessive, due to TCF3 defect
Primary IDs: OMIM:616941 ;   OMIM:619824

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