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Pathways
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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
inborn genetic disease pathway +   
Those diseases that are caused by genetic mutations present during fetal development and that may be inherited from a parent or acquired in utero. The mutations can disrupt one or several pathways that give rise to a broad spectrum of conditions affecting many types of organs and/or tissues.

Synonyms
Definition Sources: MeSH:D030342

paths to the root