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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Finger agnosia (HP:0010525)help
Term ID: 10525
Name: Finger agnosia
Synonym:
Definition: An inability or difficulty differentiating among the fingers of either hand as well as the hands of others.
Comments:
Reference: HP:0010525
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAstereognosia (HP:0010527) help
..expandProsopagnosia (HP:0010528) 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:0010525HP:0010525Finger agnosia0ABCA7 CL E G H1034737ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040283 - Occasional3
HP:0010525HP:0010525Finger agnosia0APP CL E G H351620ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040283 - Occasional74
HP:0010525HP:0010525Finger agnosia0PSEN1 CL E G H56639508ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040283 - Occasional241
HP:0010525HP:0010525Finger agnosia0PSEN2 CL E G H56649509ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040283 - Occasional59
HP:0010525HP:0010525Finger agnosia0SORL1 CL E G H665311185ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040283 - Occasional3
HP:0010525HP:0010525Finger agnosia0TOMM40 CL E G H1045218001ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040283 - Occasional
HP:0010525HP:0010525Finger agnosia0TREM2 CL E G H5420917761ORPHA:1020Early-onset autosomal dominant Alzheimer diseaseHP:0040283 - Occasional31


Genes (7) :ABCA7 APP PSEN1 PSEN2 SORL1 TOMM40 TREM2

Diseases (1) :ORPHA:1020
 

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