Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Grandparent Node:
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Abnormal tongue physiology (HP:0030810)help
Parent Node:
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Abnormality of taste sensation (HP:0000223)help
..Starting node
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Hypogeusia (HP:0000224)help
Term ID: 224
Name: Hypogeusia
Synonym: Decreased taste; Decreased taste sensation
Definition: A decreased ability to perceive flavor.
Comments:
Reference: HP:0000224
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandParageusia (HP:0031249) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0000224HP:0000224Hypogeusia0ELP1 CL E G H8518223900Familial dysautonomia223900C0013364OMIM111815959603722
HP:0000224HP:0000224Hypogeusia0ELP1 CL E G H8518223900Familial dysautonomia223900C0013364OMIM110545959603722
HP:0000224HP:0000224Hypogeusia0KIF1A CL E G H547201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM11735888601255
HP:0000224HP:0000224Hypogeusia0KIF1A CL E G H547201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM11441888601255
HP:0000224HP:0000224Hypogeusia0RETREG1 CL E G H54463201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM141625964613114
HP:0000224HP:0000224Hypogeusia0RETREG1 CL E G H54463201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM136825964613114
HP:0000224HP:0000224Hypogeusia0SCN9A CL E G H6335201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1170810597603415
HP:0000224HP:0000224Hypogeusia0SCN9A CL E G H6335201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1143810597603415
HP:0000224HP:0000224Hypogeusia0SLC39A4 CL E G H55630201100Hereditary acrodermatitis enteropathica201100C0221036OMIM148617129607059
HP:0000224HP:0000224Hypogeusia0SLC39A4 CL E G H55630201100Hereditary acrodermatitis enteropathica201100C0221036OMIM144917129607059
HP:0000224HP:0000224Hypogeusia0WNK1 CL E G H65125201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1125814540605232
HP:0000224HP:0000224Hypogeusia0WNK1 CL E G H65125201300Hereditary sensory and autonomic neuropathy type IIA201300C2752089OMIM1109614540605232
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (6) :ELP1 KIF1A RETREG1 SCN9A SLC39A4 WNK1

Diseases (3) :223900 201300 201100
 

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