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Achondroplasia and Swiss Type Agammaglobulinemia (DOID:9008779)
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Parent Terms Term With Siblings Child Terms
achondroplasia +     
agammaglobulinemia +     
achondrogenesis type IA  
achondrogenesis type IB  
achondrogenesis type II  
Achondrogenesis, Type 3 
Achondrogenesis, Type 4 
Achondroplasia and Swiss Type Agammaglobulinemia 
Achondroplastic Dwarfism  
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 
autosomal recessive osteopetrosis 7  
Baby Rattle Pelvic Dysplasia 
common variable immunodeficiency +   
Dyssegmental Dysplasia, Rolland-Desbuquois Type 
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 
Pseudoachondroplastic Dysplasia 2 
Say Barber Miller Syndrome 
Short-Limb Skeletal Dysplasia with Severe Combined Immunodeficiency 
thanatophoric dysplasia +   
transient hypogammaglobulinemia +  
X-linked agammaglobulinemia +   
X-Linked Hypogammaglobulinemia  

Exact Synonyms: Agammaglobulinaemia and achondroplasia
Primary IDs: MESH:C536020
Alternate IDs: RDO:0001430

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