Excessive salivation

Symptom Information:

Symptom ID: HPO:0003781
Synonyms:
Excessive salivation - symptom (finding) [Orphanet:27060]
Excessive salivation (disorder) [Orphanet:27060]
Sialorrhea [Orphanet:27060]
Excessive salivation [OMIM:Excessive salivation]
Hypersialorrhea [Orphanet:27060]
Salivary hypersecretion [Orphanet:27060]
Salivary hypersecretion [MedDRA:10039424]
Hypersalivation [MedDRA:10039424]
Increased salivation [MedDRA:10039424]
Ptyalism [MedDRA:10039424]
Saliva increased [MedDRA:10039424]
Saliva secretion excessive [MedDRA:10039424]
Saliva secretion increased [MedDRA:10039424]
Salivation [MedDRA:10039424]
Sialorrhoea [MedDRA:10039424]
Sialorrhea [MedDRA:10039424]
Hypersalivation [OMIM:Hypersalivation]
Quality:
Cross references:
HPO:0002307 "Drooling" [Orphanet:27060]
Orphanet:27060 "Hypersialorrhea" [Orphanet:27060]
OMIM: "Excessive salivation" [OMIM:Excessive salivation]
OMIM: "Hypersalivation" [OMIM:Hypersalivation]
UMLS:C0037036 "Sialorrhea" [Orphanet:27060]
Is a (Direct Parents):
MedDRA Oral dryness and saliva altered
Orphanet Functional anomalies of the digestive system
HPO         Abnormality of salivation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of salivation(HPO:0100755)
                         Excessive salivation(HPO:0003781)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Salivary gland conditions(MedDRA:10039404)
       Oral dryness and saliva altered(MedDRA:10030975)
          Excessive salivation(HPO:0003781)
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

14q12 microdeletion syndrome (Orphanet:261144)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Dihydropteridine reductase deficiency (Orphanet:226)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Infant botulism (Orphanet:178478)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Locked-in syndrome (Orphanet:2406)
Lyell syndrome (Orphanet:537)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Mowat-Wilson syndrome (Orphanet:2152)
Rabies (Orphanet:770)
Stevens-Johnson syndrome (Orphanet:36426)
Wilson disease (Orphanet:905)