Human Phenotype Ontology 
Grandparent Node:
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Abnormality of higher mental function (HP:0011446)help
Parent Node:
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Neurological speech impairment (HP:0002167)help
..Starting node
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Grammar-specific speech disorder (HP:0006977)help
Term ID: 6977
Name: Grammar-specific speech disorder
Synonym: Grammar-specific speech disorder
Definition:
Comments:
Reference: HP:0006977
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsent speech (HP:0001344) help
..expandAlexia (HP:0010523) help
..expandAnarthria (HP:0002425) help
..expandAnomic aphasia (HP:0030784) help
..expandAphasia (HP:0002381) help
..expandDeficit in nonword repetition (HP:0002526) help
..expandDysarthria (HP:0001260) help
..expandDysgraphia (HP:0010526) help
..expandDysphasia (HP:0002357) help
..expandDysphonia (HP:0001618) help
..expandEcholalia (HP:0010529) help
..expandIncomprehensible speech (HP:0002546) help
..expandLoss of speech (HP:0002371) help
..expandMutism (HP:0002300) help
..expandPalilalia (HP:0031814) help
..expandPoor speech (HP:0002465) help
..expandScanning speech (HP:0002168) help
..expandStuttering (HP:0025268) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006977HP:0006977Grammar-specific speech disorder0C9orf72 CL E G H203228100070ORPHA117728337614260
HP:0006977HP:0006977Grammar-specific speech disorder0CHMP2B CL E G H25978100070ORPHA116024537609512
HP:0006977HP:0006977Grammar-specific speech disorder0GRN CL E G H2896100070ORPHA15944601138945
HP:0006977HP:0006977Grammar-specific speech disorder0MAPT CL E G H4137100070ORPHA15816893157140
HP:0006977HP:0006977Grammar-specific speech disorder0PSEN1 CL E G H5663100070ORPHA15019508104311
HP:0006977HP:0006977Grammar-specific speech disorder0TMEM106B CL E G H54664100070ORPHA112822407613413
HP:0006977HP:0006977Grammar-specific speech disorder0TREM2 CL E G H54209100070ORPHA115417761605086
HP:0006977HP:0006977Grammar-specific speech disorder0VCP CL E G H7415100070ORPHA160712666601023
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (9) :C9ORF72 C9orf72 CHMP2B GRN MAPT PSEN1 TMEM106B TREM2 VCP

Diseases (1) :100070
 

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