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Keyword
  

Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Congenital Abnormalities +   
Fetal Diseases +   
genetic disease +   
Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
Hemorrhagic Shock and Encephalopathy Syndrome 
Infant, Newborn, Diseases +   
 CADASIL +   
 CAKUT2  
 cherubism +   
 Dwarfism +   
 FTDALS3  
 FTDALS4  
 Marfan syndrome +   

Synonyms
Exact Synonyms: Genetic Diseases ;   Genetic Diseases, Inborn ;   Genetic Disorder ;   Genetic Disorders ;   Hereditary Disease ;   Hereditary Diseases ;   Inborn Genetic Disease ;   Single Gene Defects ;   Single-Gene Defect
Primary IDs: MESH:D030342 ;   RDO:0004759
Definition Sources: MESH:D030342, http://ghr.nlm.nih.gov/

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