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Ontology Browser

inborn genetic disease pathway (PW:0001477)
Annotations: Rat: (529) Mouse: (529) Human: (536) Chinchilla: (497) Bonobo: (517) Dog: (517) Squirrel: (506) Pig: (518)
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.

Definition Sources: MeSH:D030342

paths to the root