loading...| Preferred Name |
prosopagnosia, hereditary |
|
| Synonyms |
hereditary prosopagnosia (disease) prosopagnosia, hereditary prosopagnosia, developmental prosopagnosia, congenital congenital prosopagnosia hereditary prosopagnosia developmental prosopagnosia face blindness |
|
| Definitions |
An instance of prosopagnosia (disease) that is caused by an inherited modification of the individual's genome. |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0012484 |
|
| has_exact_synonym |
hereditary prosopagnosia (disease) prosopagnosia, hereditary |
|
| has_related_synonym |
prosopagnosia, developmental prosopagnosia, congenital congenital prosopagnosia hereditary prosopagnosia developmental prosopagnosia face blindness |
|
| label |
prosopagnosia, hereditary |
|
| prefixIRI |
MONDO:0012484 |
|
| prefLabel |
prosopagnosia, hereditary |
|
| textual definition |
An instance of prosopagnosia (disease) that is caused by an inherited modification of the individual's genome. |
|
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0012484 | MONDO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0012484 | MONDO | LOOM | |
| http://purl.bioontology.org/ontology/MESH/C537242 | MESH | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/610382 | OMIM | LOOM | |
| http://phenomebrowser.net/ontologies/mesh/mesh.owl#C537242 | RH-MESH | LOOM |