Human Phenotype Ontology 
Grandparent Node:
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Tooth agenesis (HP:0009804)help
Parent Node:
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Abnormality of premolar (HP:0011076)help
Parent Node:
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Selective tooth agenesis (HP:0001592)help
..Starting node
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Agenesis of premolar (HP:0011051)help
Term ID: 11051
Name: Agenesis of premolar
Synonym: Absence of bicuspid; Absence of premolar; Agenesis of bicuspid; Failure of development of bicuspid; Failure of development of premolar; Missing bicuspid; Missing premolar
Definition: Agenesis of premolar tooth.
Comments:
Reference: HP:0011051
Genes and Diseases:
 
       Child Nodes:
........expandAgenesis of maxillary premolar (HP:0011052) help
........expandAgenesis of mandibular premolar (HP:0011053) help

 Sister Nodes: 
..expandAgenesis of canine (HP:0012738) help
..expandAgenesis of incisor (HP:0006485) help
..expandAgenesis of molar (HP:0011054) 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:0011051HP:0011051Agenesis of premolar0AXIN2 CL E G H8313904ORPHA:99798OligodontiaHP:0040282 - Frequent435
HP:0011051HP:0011051Agenesis of premolar0EDA CL E G H18963157ORPHA:99798OligodontiaHP:0040282 - Frequent115
HP:0011051HP:0011051Agenesis of premolar0EDA CL E G H18963157OMIM:313500TOOTH AGENESIS, SELECTIVE, X-LINKED, 1; STHAGX1115
HP:0011051HP:0011051Agenesis of premolar0EDARADD CL E G H12817814341ORPHA:99798OligodontiaHP:0040282 - Frequent56
HP:0011051HP:0011051Agenesis of premolar0FGF3 CL E G H22483681ORPHA:2791Otodental syndromeHP:0040282 - Frequent18
HP:0011051HP:0011051Agenesis of premolar0FGFR1 CL E G H22603688ORPHA:99798OligodontiaHP:0040282 - Frequent172
HP:0011051HP:0011051Agenesis of premolar0IRF6 CL E G H36646121ORPHA:99798OligodontiaHP:0040282 - Frequent99
HP:0011051HP:0011051Agenesis of premolar0LRP6 CL E G H40406698ORPHA:99798OligodontiaHP:0040282 - Frequent26
HP:0011051HP:0011051Agenesis of premolar0MSX1 CL E G H44877391ORPHA:99798OligodontiaHP:0040282 - Frequent12
HP:0011051HP:0011051Agenesis of premolar0PAX9 CL E G H50838623ORPHA:99798OligodontiaHP:0040282 - Frequent58
HP:0011051HP:0011051Agenesis of premolar0SUMO1 CL E G H734112502ORPHA:99798OligodontiaHP:0040282 - Frequent8
HP:0011051HP:0011051Agenesis of premolar0TGFA CL E G H703911765ORPHA:99798OligodontiaHP:0040282 - Frequent
HP:0011051HP:0011051Agenesis of premolar0WNT10A CL E G H8032613829ORPHA:99798OligodontiaHP:0040282 - Frequent71
HP:0011051HP:0011051Agenesis of premolar0WNT10B CL E G H748012775ORPHA:99798OligodontiaHP:0040282 - Frequent4
HP:0011051HP:0011052Agenesis of maxillary premolar1 CL E G H
HP:0011051HP:0011053Agenesis of mandibular premolar1AXIN2 CL E G H8313904ORPHA:99798OligodontiaHP:0040283 - Occasional435
HP:0011051HP:0011053Agenesis of mandibular premolar1EDA CL E G H18963157ORPHA:99798OligodontiaHP:0040283 - Occasional115
HP:0011051HP:0011053Agenesis of mandibular premolar1EDARADD CL E G H12817814341ORPHA:99798OligodontiaHP:0040283 - Occasional56
HP:0011051HP:0011053Agenesis of mandibular premolar1FGFR1 CL E G H22603688ORPHA:99798OligodontiaHP:0040283 - Occasional172
HP:0011051HP:0011053Agenesis of mandibular premolar1IRF6 CL E G H36646121ORPHA:99798OligodontiaHP:0040283 - Occasional99
HP:0011051HP:0011053Agenesis of mandibular premolar1LRP6 CL E G H40406698ORPHA:99798OligodontiaHP:0040283 - Occasional26
HP:0011051HP:0011053Agenesis of mandibular premolar1MSX1 CL E G H44877391ORPHA:99798OligodontiaHP:0040283 - Occasional12
HP:0011051HP:0011053Agenesis of mandibular premolar1PAX9 CL E G H50838623ORPHA:99798OligodontiaHP:0040283 - Occasional58
HP:0011051HP:0011053Agenesis of mandibular premolar1SUMO1 CL E G H734112502ORPHA:99798OligodontiaHP:0040283 - Occasional8
HP:0011051HP:0011053Agenesis of mandibular premolar1TGFA CL E G H703911765ORPHA:99798OligodontiaHP:0040283 - Occasional
HP:0011051HP:0011053Agenesis of mandibular premolar1WNT10A CL E G H8032613829ORPHA:99798OligodontiaHP:0040283 - Occasional71
HP:0011051HP:0011053Agenesis of mandibular premolar1WNT10B CL E G H748012775ORPHA:99798OligodontiaHP:0040283 - Occasional4


Genes (13) :AXIN2 EDA EDARADD FGF3 FGFR1 IRF6 LRP6 MSX1 PAX9 SUMO1 TGFA WNT10A WNT10B

Diseases (3) :ORPHA:99798 OMIM:313500 ORPHA:2791
 

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