Human Phenotype Ontology 
Grandparent Node:
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Abnormality of higher mental function (HP:0011446)help
Parent Node:
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Agnosia (HP:0010524)help
..Starting node
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Prosopagnosia (HP:0010528)help
Term ID: 10528
Name: Prosopagnosia
Synonym: Face blindness; Facial agnosia
Definition: Inability to recognize faces of familiar persons.
Comments:
Reference: HP:0010528
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAstereognosia (HP:0010527) help
..expandFinger agnosia (HP:0010525) help
..expandVisual agnosia (HP:0030222) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010528HP:0010528Prosopagnosia0EPRS1 CL E G H20583418OMIM:617951Leukodystrophy, hypomyelinating, 15


Genes (1) :EPRS1

Diseases (1) :OMIM:617951
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.