Human Phenotype Ontology 
Grandparent Node:
expandMorphological central nervous system abnormality (HP:0002011)help
Parent Node:
expandAbnormal cerebrospinal fluid morphology (HP:0002921)help
..Starting node
..expandCerebrospinal fluid rhinorrhoea (HP:0030998)help
Term ID: 30998
Name: Cerebrospinal fluid rhinorrhoea
Synonym: CSF rhinorrhoea
Definition: Drainage of cerebrospinal fluid through the nose. This can occur when there is a fistula between the dura and the skull base and discharge of cerebrospinal fluid (CSF) from the nose.
Comments:
Reference: HP:0030998
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal CSF metabolite concentration (HP:0025454) help
..expandAbnormal CSF protein concentration (HP:0025456) help
..expandAbnormal CSF/serum albumin ratio (HP:0030981) help
..expandCSF pleocytosis (HP:0012229) help
..expandExtra-axial cerebrospinal fluid accumulation (HP:0012510) help
..expandHydrocephalus (HP:0000238) 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:0030998HP:0030998Cerebrospinal fluid rhinorrhoea0IGHG2 CL E G H35015526ORPHA:183675Recurrent infections associated with rare immunoglobulin isotypes deficiency1
HP:0030998HP:0030998Cerebrospinal fluid rhinorrhoea0IGKC CL E G H35145716ORPHA:183675Recurrent infections associated with rare immunoglobulin isotypes deficiency5


Genes (2) :IGHG2 IGKC

Diseases (1) :ORPHA:183675
 

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