| Term ID: |
31416 |
| Name: |
Abnormal nasal mucus secretion |
| Synonym: |
|
| Definition: |
Any deviation from the normal quantity of secretion of nasal mucus, a thick viscous liquid produced by the mucous membranes of the nose. |
| Comments: |
|
| Reference: |
HP:0031416 |
| Genes and Diseases: | |
Child Nodes: |
........ Rhinorrhea (HP:0031417) 
|
Sister Nodes: |
..Abnormal blood gas level (HP:0012415)
|
..Abnormal breath sound (HP:0030829)
|
..Abnormal bronchus physiology (HP:0025427)
|
..Abnormal mucociliary clearance (HP:0031602)
|
..Abnormal pattern of respiration (HP:0002793)
|
..Abnormal respiratory motile cilium physiology (HP:0012261)
|
..Abnormal response to short acting pulmonary vasodilator (HP:0030893)
|
..Abnormality of pulmonary circulation (HP:0030875)
|
..Abnormality on pulmonary function testing (HP:0030878)
|
..Airway obstruction (HP:0006536)
|
..Aspiration (HP:0002835)
|
..Asthma (HP:0002099)
|
..Breathing dysregulation (HP:0005957)
|
..Cough (HP:0012735)
|
..Cyanosis (HP:0000961)
|
..Dyspnea (HP:0002094)
|
..obsolete Decreased pulmonary function (HP:0005952)
|
..Recurrent singultus (HP:0100247)
|
..Reduced vital capacity (HP:0002792)
|
..Respiratory insufficiency (HP:0002093)
|
..Restrictive ventilatory defect (HP:0002091)
|
..Sneeze (HP:0025095)
|
..Snoring (HP:0025267)
|
..Tracheal tug on inspiration (HP:0025008)
|
..Upper airway obstruction (HP:0002781)
|
..Weakness of muscles of respiration (HP:0004347)
|
| Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
|---|
HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | CCDC39 CL E G H | 339829 | 25244 | OMIM:613807 | Ciliary dyskinesia, primary, 14 | | | | 126 | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | CCDC40 CL E G H | 55036 | 26090 | OMIM:613808 | CILIARY DYSKINESIA, PRIMARY, 15; CILD15 | | | | 182 | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | DNAH1 CL E G H | 25981 | 2940 | OMIM:617577 | Ciliary dyskinesia, primary, 37 | | | | 21 | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | LRRC56 CL E G H | 115399 | 25430 | OMIM:618254 | CILIARY DYSKINESIA, PRIMARY, 39; CILD39 | | | | | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | ODAD1 CL E G H | 93233 | 26560 | OMIM:615067 | Ciliary dyskinesia, primary, 20 | | | | | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | SCN9A CL E G H | 6335 | 10597 | OMIM:167400 | Paroxysmal extreme pain disorder | | | | 318 | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | SDHD CL E G H | 6392 | 10683 | ORPHA:100093 | Carcinoid syndrome | | | | 129 | | | | HP:0031416 | HP:0031416 | Abnormal nasal mucus secretion | 0 | SREBF1 CL E G H | 6720 | 11289 | OMIM:158310 | Mucoepithelial dysplasia, hereditary | | | | 1 | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | CCDC39 CL E G H | 339829 | 25244 | OMIM:613807 | Ciliary dyskinesia, primary, 14 | | | | 126 | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | CCDC40 CL E G H | 55036 | 26090 | OMIM:613808 | CILIARY DYSKINESIA, PRIMARY, 15; CILD15 | | | | 182 | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | DNAH1 CL E G H | 25981 | 2940 | OMIM:617577 | Ciliary dyskinesia, primary, 37 | . | | | 21 | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | LRRC56 CL E G H | 115399 | 25430 | OMIM:618254 | CILIARY DYSKINESIA, PRIMARY, 39; CILD39 | | | | | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | ODAD1 CL E G H | 93233 | 26560 | OMIM:615067 | Ciliary dyskinesia, primary, 20 | . | | | | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | SCN9A CL E G H | 6335 | 10597 | OMIM:167400 | Paroxysmal extreme pain disorder | . | | | 318 | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | SDHD CL E G H | 6392 | 10683 | ORPHA:100093 | Carcinoid syndrome | HP:0040283 - Occasional | | | 129 | | | | HP:0031416 | HP:0031417 | Rhinorrhea | 1 | SREBF1 CL E G H | 6720 | 11289 | OMIM:158310 | Mucoepithelial 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.
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