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loading...| Preferred Name |
Prosopagnosia, hereditary |
|
| Synonyms |
Prosopagnosia, congenital |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C537242 |
|
| altLabel |
Prosopagnosia, congenital Face blindness |
|
| cui |
C2931455 |
|
| Has mapping qualifier | ||
| HM |
D020238/Q000151 |
|
| Inverse of RB |
0 |
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| Mapped to | ||
| MDA |
20100825 |
|
| MeSH Frequency |
45 |
|
| MMR |
20150818 |
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| notation |
C537242 |
|
| prefLabel |
Prosopagnosia, hereditary |
|
| SC |
3 |
|
| Scope Statement |
A hereditary form of prosopagnosia, or inability to recognize someone by face alone in the absence of sensory or intellectual impairment. It appears to exhibit autosomal dominant inheritance and may affect 0.75-2% of different populations. OMIM: 610382 |
|
| TERMUI |
T741920 T741919 T741918 |
|
| TH |
OMIM (2013) ORD (2010) |
|
| tui |
T047 |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/OMIM/610382 | OMIM | CUI | |
| http://purl.obolibrary.org/obo/MONDO_0012484 | MONDO | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/610382 | OMIM | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0012484 | DOVES | LOOM | |
| http://phenomebrowser.net/ontologies/mesh/mesh.owl#C537242 | RH-MESH | LOOM |