Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the tongue (HP:0000157)help
Parent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Abnormal tongue physiology (HP:0030810)help
..Starting node
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Abnormality of taste sensation (HP:0000223)help
Term ID: 223
Name: Abnormality of taste sensation
Synonym: Abnormality of taste sensation
Definition:
Comments:
Reference: HP:0000223
Genes and Diseases:
 
       Child Nodes:
........expandDecreased taste sensation (HP:0000224) help
........expandParageusia (HP:0031249) help

 Sister Nodes: 
..expandMovement abnormality of the tongue (HP:0000182) help
..expandTongue fasciculations (HP:0001308) help
..expandTongue pain (HP:0030811) 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:0000223HP:0000223Abnormality of taste sensation0ELP1 CL E G H85185959OMIM:223900Neuropathy, hereditary sensory and autonomic, type III133
HP:0000223HP:0000223Abnormality of taste sensation0KIF1A CL E G H547888OMIM:201300Neuropathy, hereditary sensory and autonomic, type II276
HP:0000223HP:0000223Abnormality of taste sensation0RETREG1 CL E G H5446325964OMIM:201300Neuropathy, hereditary sensory and autonomic, type II54
HP:0000223HP:0000223Abnormality of taste sensation0SCN9A CL E G H633510597OMIM:201300Neuropathy, hereditary sensory and autonomic, type II318
HP:0000223HP:0000223Abnormality of taste sensation0SLC39A4 CL E G H5563017129OMIM:201100Acrodermatitis enteropathica, Zinc-Deficiency type55
HP:0000223HP:0000223Abnormality of taste sensation0WNK1 CL E G H6512514540OMIM:201300Neuropathy, hereditary sensory and autonomic, type II199
HP:0000223HP:0041051Ageusia1 CL E G H
HP:0000223HP:0033847Phantageusia1 CL E G H
HP:0000223HP:0031249Parageusia1 CL E G H
HP:0000223HP:0000224Hypogeusia1ELP1 CL E G H85185959OMIM:223900Neuropathy, hereditary sensory and autonomic, type III.133
HP:0000223HP:0000224Hypogeusia1KIF1A CL E G H547888OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.276
HP:0000223HP:0000224Hypogeusia1RETREG1 CL E G H5446325964OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.54
HP:0000223HP:0000224Hypogeusia1SCN9A CL E G H633510597OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.318
HP:0000223HP:0000224Hypogeusia1SLC39A4 CL E G H5563017129OMIM:201100Acrodermatitis enteropathica, Zinc-Deficiency type.55
HP:0000223HP:0000224Hypogeusia1WNK1 CL E G H6512514540OMIM:201300Neuropathy, hereditary sensory and autonomic, type II.199


Genes (6) :ELP1 KIF1A RETREG1 SCN9A SLC39A4 WNK1

Diseases (3) :OMIM:223900 OMIM:201300 OMIM:201100
 

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