Human Phenotype Ontology 
Grandparent Node:
expandAbnormal ear physiology (HP:0031704)help
Parent Node:
expandHearing abnormality (HP:0000364)help
..Starting node
..expandAbnormal speech discrimination (HP:0001963)help
Term ID: 1963
Name: Abnormal speech discrimination
Synonym: Abnormal speech discrimination; Poor speech discrimination
Definition: A type of hearing impairment prominently characterized by a difficulty in understanding speech, rather than an inability to hear speech. Poor speech discrimination is a very common symptom of high frequency hearing loss.
Comments:
Reference: HP:0001963
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHearing impairment (HP:0000365) help
..expandTinnitus (HP:0000360) 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:0001963HP:0001963Abnormal speech discrimination0AIFM1 CL E G H91318768OMIM:300614Deafness, X-linked 5.60
HP:0001963HP:0001963Abnormal speech discrimination0DIAPH3 CL E G H8162415480OMIM:609129Auditory neuropathy, autosomal dominant, 1.8
HP:0001963HP:0001963Abnormal speech discrimination0KPTN CL E G H111336404ORPHA:397612Macrocephaly-developmental delay syndromeHP:0040282 - Frequent13
HP:0001963HP:0001963Abnormal speech discrimination0TMEM43 CL E G H7918828472OMIM:619832AUDITORY NEUROPATHY, AUTOSOMAL DOMINANT 3; AUNA3171


Genes (4) :AIFM1 DIAPH3 KPTN TMEM43

Diseases (4) :OMIM:300614 OMIM:609129 ORPHA:397612 OMIM:619832
 

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