Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Abnormal central sensory function (HP:0011730)help
..Starting node
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Agraphesthesia (HP:0011812)help
Term ID: 11812
Name: Agraphesthesia
Synonym:
Definition: Impaired ability to recognize letters or numbers drawn by an examiner's fingertip on the patient's skin (the patients eyes are closed or covered throughout this examination).
Comments:
Reference: HP:0011812
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAstereognosia (HP:0010527) help
..expandImpaired touch localization (HP:0011811) help
..expandImpaired two-point discrimination (HP:0011810) 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:0011812HP:0011812Agraphesthesia0ATP6AP2 CL E G H1015918305OMIM:300423MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH36
HP:0011812HP:0011812Agraphesthesia0ATP6AP2 CL E G H1015918305ORPHA:93952X-linked intellectual disability, Hedera typeHP:0040283 - Occasional36


Genes (1) :ATP6AP2

Diseases (2) :OMIM:300423 ORPHA:93952
 

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