Human Phenotype Ontology 
Grandparent Node:
expandAbnormal respiratory system physiology (HP:0002795)help
Parent Node:
expandAbnormal nasal mucus secretion (HP:0031416)help
..Starting node
..expandRhinorrhea (HP:0031417)help
Term ID: 31417
Name: Rhinorrhea
Synonym: Nasal Discharge; Runny Nose
Definition: Increased discharge of mucus from the nose.
Comments:
Reference: HP:0031417
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031417HP:0031417Rhinorrhea0CCDC39 CL E G H33982925244OMIM:613807Ciliary dyskinesia, primary, 14126
HP:0031417HP:0031417Rhinorrhea0CCDC40 CL E G H5503626090OMIM:613808CILIARY DYSKINESIA, PRIMARY, 15; CILD15182
HP:0031417HP:0031417Rhinorrhea0DNAH1 CL E G H259812940OMIM:617577Ciliary dyskinesia, primary, 37.21
HP:0031417HP:0031417Rhinorrhea0LRRC56 CL E G H11539925430OMIM:618254CILIARY DYSKINESIA, PRIMARY, 39; CILD39
HP:0031417HP:0031417Rhinorrhea0ODAD1 CL E G H9323326560OMIM:615067Ciliary dyskinesia, primary, 20.
HP:0031417HP:0031417Rhinorrhea0SCN9A CL E G H633510597OMIM:167400Paroxysmal extreme pain disorder.318
HP:0031417HP:0031417Rhinorrhea0SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040283 - Occasional129
HP:0031417HP:0031417Rhinorrhea0SREBF1 CL E G H672011289OMIM:158310Mucoepithelial dysplasia, hereditary.1


Genes (8) :CCDC39 CCDC40 DNAH1 LRRC56 ODAD1 SCN9A SDHD SREBF1

Diseases (8) :OMIM:613807 OMIM:613808 OMIM:617577 OMIM:618254 OMIM:615067 OMIM:167400 ORPHA:100093 OMIM:158310
 

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