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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Smooth tongue (HP:0010298)help
Term ID: 10298
Name: Smooth tongue
Synonym: Atrophy of dorsum of tongue; Atrophy of lingual surface; Atrophy of tongue surface; Smooth dorsum of tongue; Smooth lingual surface; Smooth surface of tongue; Smooth tongue
Definition: Glossy appearance of the entire tongue surface.
Comments:
Reference: HP:0010298
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
..expandGlossitis (HP:0000206) 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
..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:0010298HP:0010298Smooth tongue0KRT14 CL E G H38616416ORPHA:79396Autosomal dominant generalized epidermolysis bullosa simplex, severe formHP:0040283 - Occasional110
HP:0010298HP:0010298Smooth tongue0KRT5 CL E G H38526442ORPHA:79396Autosomal dominant generalized epidermolysis bullosa simplex, severe formHP:0040283 - Occasional173
HP:0010298HP:0010298Smooth tongue0LIFR CL E G H39776597ORPHA:3206Stüve-Wiedemann syndromeHP:0040282 - Frequent144
HP:0010298HP:0010298Smooth tongue0LIFR CL E G H39776597OMIM:601559Stuve-Wiedemann syndrome.144
HP:0010298HP:0010298Smooth tongue0WNT10A CL E G H8032613829OMIM:257980Odontoonychodermal dysplasia.71


Genes (4) :KRT14 KRT5 LIFR WNT10A

Diseases (4) :ORPHA:79396 ORPHA:3206 OMIM:601559 OMIM:257980
 

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