Human Phenotype Ontology 
Grandparent Node:
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Abnormality of higher mental function (HP:0011446)help
Parent Node:
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Abnormal central sensory function (HP:0011730)help
Parent Node:
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Agnosia (HP:0010524)help
..Starting node
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Astereognosia (HP:0010527)help
Term ID: 10527
Name: Astereognosia
Synonym: Astereognosis; Somatosensory agnosia
Definition: Inability to recognize the form of objects by touch without visual input. That is, an impairment in the recognition of objects based only on the texture, size, weight and three-dimensional form of the object in the absence of any major somatosensory deficit.
Comments:
Reference: HP:0010527
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandFinger agnosia (HP:0010525) help
..expandProsopagnosia (HP:0010528) help
..expandVisual agnosia (HP:0030222) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0010527HP:0010527Astereognosia0ATP6AP2 CL E G H10159300423Mental retardation, X-linked, syndromic, Hedera type300423C1845543OMIM128618305300556
HP:0010527HP:0010527Astereognosia0ATP6AP2 CL E G H10159300423Mental retardation, X-linked, syndromic, Hedera type300423C1845543OMIM126318305300556
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :ATP6AP2

Diseases (1) :300423
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.