loading...| Preferred Name |
inborn genetic disease pathway |
| Definitions |
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. |
| ID |
http://purl.obolibrary.org/obo/PW_0001477 |
| created_by |
VPetri |
| creation_date |
2013-10-31T10:54:45Z |
| definition |
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. |
| has_obo_namespace |
pathway |
| id |
PW:0001477 |
| label |
inborn genetic disease pathway |
| notation |
PW:0001477 |
| prefLabel |
inborn genetic disease pathway |
| treeView | |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||