Human Phenotype Ontology 
Grandparent Node:
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Abnormal salivary gland morphology (HP:0010286)help
Parent Node:
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Abnormal parotid gland morphology (HP:0000197)help
..Starting node
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Absence of Stensen duct (HP:0000198)help
Term ID: 198
Name: Absence of Stensen duct
Synonym: Absence of parotid duct; Absent stensen duct; Agenesis of parotid duct; Agenesis of stensen duct; Failure of development of parotid duct; Failure of development of stensen duct; Missing parotid duct; Missing stensen duct
Definition:
Comments:
Reference: HP:0000198
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAplasia of the parotid gland (HP:0009740) help
..expandEnlargement of parotid gland (HP:0011801) help
..expandParotitis (HP:0011850) 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:0000198HP:0000198Absence of Stensen duct0FGF10 CL E G H22553666OMIM:149730Lacrimoauriculodentodigital syndrome.17
HP:0000198HP:0000198Absence of Stensen duct0FGFR2 CL E G H22633689OMIM:149730Lacrimoauriculodentodigital syndrome.175
HP:0000198HP:0000198Absence of Stensen duct0FGFR3 CL E G H22613690OMIM:149730Lacrimoauriculodentodigital syndrome.145
HP:0000198HP:0000198Absence of Stensen duct0TP63 CL E G H862615979OMIM:604292Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3.140


Genes (4) :FGF10 FGFR2 FGFR3 TP63

Diseases (2) :OMIM:149730 OMIM:604292
 

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