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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 +   
Sandestig-Stefanova Syndrome  
 CADASIL +   
 CAKUT2  
 Dwarfism +   
 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
Xrefs: NCI:C3101
Definition Sources: http://ghr.nlm.nih.gov/ "DO", MESH:D030342

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