Prosopagnosia

Symptom Information:

Symptom ID: HPO:0010528
Synonyms:
Face blindness [HPO:0010528]
Facial agnosia [HPO:0010528]
Propopagnosia [Orphanet:43550]
Visual/auditory/tactile agnosia/propopagnosia/simultagnosia [Orphanet:43550]
Auditory agnosia [Orphanet:43550]
Auditory agnosia (finding) [Orphanet:43550]
Visual agnosia [Orphanet:43550]
Visual agnosia (disorder) [Orphanet:43550]
Visual Agnosia [Orphanet:43550]
Simultagnosia [Orphanet:43550]
Simultagnosia (finding) [Orphanet:43550]
Astereognosis [MedDRA:10056477]
Tactile agnosia [Orphanet:43550]
Tactile agnosia (finding) [Orphanet:43550]
Tactile Agnosia [Orphanet:43550]
Prosopagnosia [MedDRA:10073980]
Quality:
Cross references:
Orphanet:43550 "Visual/auditory/tactile agnosia/propopagnosia/simultagnosia" [Orphanet:43550]
UMLS:C0234512 "Prosopagnosia" [HPO:0010528]
UMLS:C0234501 "Auditory agnosia" [Orphanet:43550]
UMLS:C0234502 "Visual Agnosia" [Orphanet:43550]
UMLS:C0563620 "Simultagnosia" [Orphanet:43550]
UMLS:C0234505 "Tactile Agnosia" [Orphanet:43550]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
HPO         Agnosia
Orphanet Astereognosia
MedDRA Specific cognitive ability disturbances
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Agnosia(HPO:0010524)
                   Prosopagnosia(HPO:0010528)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

PROSOPAGNOSIA, HEREDITARY (OMIM:610382)