Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the dentition (HP:0000164)help
Grandparent Node:
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Neoplasm of the oral cavity (HP:0100649)help
Parent Node:
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Odontogenic neoplasm (HP:0100612)help
..Starting node
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Odontogenic keratocysts of the jaw (HP:0010603)help
Term ID: 10603
Name: Odontogenic keratocysts of the jaw
Synonym: Keratocystic odontogenic tumor; Keratocystic odontogenic tumour; Keratocysts of the jaw
Definition: A benign uni- or multicystic, intraosseous tumor of odontogenic origin, with a characteristic lining of parakeratinized stratified squamous epithelium and potential for aggressive, infiltrative behaviour.
Comments:
Reference: HP:0010603
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCementoma (HP:0012328) help
..expandOdontoma (HP:0011068) 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:0010603HP:0010603Odontogenic keratocysts of the jaw0PTCH1 CL E G H57279585OMIM:109400Basal cell nevus syndrome665
HP:0010603HP:0010603Odontogenic keratocysts of the jaw0PTCH1 CL E G H57279585ORPHA:77301Monosomy 9q22.3HP:0040281 - Very frequent665
HP:0010603HP:0010603Odontogenic keratocysts of the jaw0PTCH2 CL E G H86439586OMIM:109400Basal cell nevus syndrome40
HP:0010603HP:0010603Odontogenic keratocysts of the jaw0SUFU CL E G H5168416466OMIM:109400Basal cell nevus syndrome124


Genes (3) :PTCH1 PTCH2 SUFU

Diseases (2) :OMIM:109400 ORPHA:77301
 

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