Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of higher mental function (HP:0011446)help
Parent Node:
expand
Agnosia (HP:0010524)help
..Starting node
..expand
Visual agnosia (HP:0030222)help
Term ID: 30222
Name: Visual agnosia
Synonym:
Definition: Difficulty in recognizing objects by visual input in absence of sensorial visual impairment.
Comments:
Reference: HP:0030222
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAstereognosia (HP:0010527) help
..expandFinger agnosia (HP:0010525) help
..expandProsopagnosia (HP:0010528) 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:0030222HP:0030222Visual agnosia0ABCD1 CL E G H21561ORPHA:139396X-linked cerebral adrenoleukodystrophyHP:0040283 - Occasional135
HP:0030222HP:0030222Visual agnosia0C9ORF72 CL E G H20322828337ORPHA:100069Semantic dementiaHP:0040281 - Very frequent56
HP:0030222HP:0030222Visual agnosia0CEP85L CL E G H38711921638OMIM:618873LISSENCEPHALY 10; LIS101
HP:0030222HP:0030222Visual agnosia0CHMP2B CL E G H2597824537ORPHA:100069Semantic dementiaHP:0040281 - Very frequent42
HP:0030222HP:0030222Visual agnosia0GRN CL E G H28964601ORPHA:100069Semantic dementiaHP:0040281 - Very frequent126
HP:0030222HP:0030222Visual agnosia0MAPT CL E G H41376893ORPHA:100069Semantic dementiaHP:0040281 - Very frequent140
HP:0030222HP:0030222Visual agnosia0PSEN1 CL E G H56639508ORPHA:100069Semantic dementiaHP:0040281 - Very frequent241
HP:0030222HP:0030222Visual agnosia0TMEM106B CL E G H5466422407ORPHA:100069Semantic dementiaHP:0040281 - Very frequent
HP:0030222HP:0030222Visual agnosia0TREM2 CL E G H5420917761ORPHA:100069Semantic dementiaHP:0040281 - Very frequent31


Genes (9) :ABCD1 C9ORF72 CEP85L CHMP2B GRN MAPT PSEN1 TMEM106B TREM2

Diseases (3) :ORPHA:139396 ORPHA:100069 OMIM:618873
 

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