Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the tongue (HP:0000157)help
Parent Node:
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Abnormal tongue morphology (HP:0030809)help
..Starting node
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Glossitis (HP:0000206)help
Term ID: 206
Name: Glossitis
Synonym: Inflammation of the tongue; Lingual inflammation; Smooth swollen tongue
Definition: Inflammation of the tongue.
Comments:
Reference: HP:0000206
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal hyoglossus muscle morphology (HP:3000051) help
..expandAbnormal lingual artery morphology (HP:3000074) help
..expandAbnormality of lingual tonsil (HP:3000076) help
..expandAbnormality of the tongue muscle (HP:0040173) help
..expandAnkyloglossia (HP:0010296) help
..expandAplasia/Hypoplasia of the tongue (HP:0010295) help
..expandBifid tongue (HP:0010297) help
..expandDuplicated tongue (HP:0040294) help
..expandFurrowed tongue (HP:0000221) help
..expandGeographic tongue (HP:0025252) help
..expandGlossoptosis (HP:0000162) help
..expandLobulated tongue (HP:0000180) help
..expandMacroglossia (HP:0000158) help
..expandPosteriorly placed tongue (HP:0009087) help
..expandProtruding tongue (HP:0010808) help
..expandSmooth tongue (HP:0010298) help
..expandStiff tongue (HP:0031373) help
..expandStrawberry tongue (HP:0031042) help
..expandTongue atrophy (HP:0012473) help
..expandTongue nodules (HP:0000199) help
..expandTongue telangiectasia (HP:0000227) 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:0000206HP:0000206Glossitis0AMN CL E G H8169314604ORPHA:35858Imerslund-Gräsbeck syndromeHP:0040283 - Occasional25
HP:0000206HP:0000206Glossitis0CLTRN CL E G H5739329437ORPHA:2116Hartnup diseaseHP:0040283 - Occasional
HP:0000206HP:0000206Glossitis0CUBN CL E G H80292548ORPHA:35858Imerslund-Gräsbeck syndromeHP:0040283 - Occasional273
HP:0000206HP:0000206Glossitis0HLA-B CL E G H31064932ORPHA:397Giant cell arteritisHP:0040283 - Occasional4
HP:0000206HP:0000206Glossitis0HLA-DRB1 CL E G H31234948ORPHA:397Giant cell arteritisHP:0040283 - Occasional2
HP:0000206HP:0000206Glossitis0LMBRD1 CL E G H5578823038ORPHA:79284Methylmalonic acidemia with homocystinuria type cblFHP:0040283 - Occasional46
HP:0000206HP:0000206Glossitis0LMBRD1 CL E G H5578823038OMIM:277380Methylmalonic aciduria and homocystinuria, Cblf type.46
HP:0000206HP:0000206Glossitis0MMACHC CL E G H2597424525ORPHA:79282Methylmalonic acidemia with homocystinuria, type cblCHP:0040282 - Frequent101
HP:0000206HP:0000206Glossitis0P4HA2 CL E G H89748547ORPHA:397Giant cell arteritisHP:0040283 - Occasional3
HP:0000206HP:0000206Glossitis0PTPN22 CL E G H261919652ORPHA:397Giant cell arteritisHP:0040283 - Occasional3
HP:0000206HP:0000206Glossitis0SLC39A4 CL E G H5563017129ORPHA:37Acrodermatitis enteropathicaHP:0040282 - Frequent55
HP:0000206HP:0000206Glossitis0SLC46A1 CL E G H11323530521ORPHA:90045Hereditary folate malabsorptionHP:0040281 - Very frequent101
HP:0000206HP:0000206Glossitis0SLC6A19 CL E G H34002427960ORPHA:2116Hartnup diseaseHP:0040283 - Occasional12
HP:0000206HP:0000206Glossitis0SLC6A19 CL E G H34002427960OMIM:234500Hartnup disorderHP:0040283 - Occasional12


Genes (12) :AMN CLTRN CUBN HLA-B HLA-DRB1 LMBRD1 MMACHC P4HA2 PTPN22 SLC39A4 SLC46A1 SLC6A19

Diseases (9) :ORPHA:35858 ORPHA:2116 ORPHA:397 ORPHA:79284 OMIM:277380 ORPHA:79282 ORPHA:37 ORPHA:90045 OMIM:234500
 

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