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
..expand
Incomprehensible speech (HP:0002546)help
Term ID: 2546
Name: Incomprehensible speech
Synonym: Incomprehensible speech
Definition:
Comments:
Reference: HP:0002546
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
..expandDysphonia (HP:0001618) help
..expandEcholalia (HP:0010529) help
..expandGrammar-specific speech disorder (HP:0006977) help
..expandLoss of speech (HP:0002371) help
..expandMutism (HP:0002300) help
..expandobsolete Dysphasia (HP:0002357) help
..expandPalilalia (HP:0031814) help
..expandPoor speech (HP:0002465) help
..expandScanning speech (HP:0002168) help
..expandStuttering (HP:0025268) 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:0002546HP:0002546Incomprehensible speech0CC2D1A CL E G H5486230237OMIM:608443Mental retardation, autosomal recessive 3.57
HP:0002546HP:0002546Incomprehensible speech0FOXP2 CL E G H9398613875ORPHA:209908Childhood apraxia of speechHP:0040282 - Frequent143
HP:0002546HP:0002546Incomprehensible speech0FOXP2 CL E G H9398613875OMIM:602081Speech-language disorder-1.143
HP:0002546HP:0002546Incomprehensible speech0FXN CL E G H23953951ORPHA:95Friedreich ataxiaHP:0040283 - Occasional18
HP:0002546HP:0002546Incomprehensible speech0GATAD2B CL E G H5745930778ORPHA:363686Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndromeHP:0040283 - Occasional33
HP:0002546HP:0002546Incomprehensible speech0GRIN2A CL E G H29034585ORPHA:163721Rolandic epilepsy-speech dyspraxia syndromeHP:0040283 - Occasional434
HP:0002546HP:0002546Incomprehensible speech0SATB2 CL E G H2331421637ORPHA:2510192q32q33 microdeletion syndromeHP:0040283 - Occasional34
HP:0002546HP:0002546Incomprehensible speech0SETBP1 CL E G H2604015573ORPHA:436151Intellectual disability-expressive aphasia-facial dysmorphism syndromeHP:0040283 - Occasional143
HP:0002546HP:0002546Incomprehensible speech0SRPX2 CL E G H2728630668ORPHA:163721Rolandic epilepsy-speech dyspraxia syndromeHP:0040283 - Occasional50


Genes (8) :CC2D1A FOXP2 FXN GATAD2B GRIN2A SATB2 SETBP1 SRPX2

Diseases (8) :OMIM:608443 ORPHA:209908 OMIM:602081 ORPHA:95 ORPHA:363686 ORPHA:163721 ORPHA:251019 ORPHA:436151
 

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