Drooling

Symptom Information:

Symptom ID: HPO:0002307
Synonyms:
Dribbling [HPO:0002307]
Sialorrhea [HPO:0002307]
Excessive salivation [Orphanet:27060]
Excessive salivation - symptom (finding) [Orphanet:27060]
Excessive salivation (disorder) [Orphanet:27060]
Sialorrhea [Orphanet:27060]
Drooling [OMIM:Drooling]
Sialorrhea [OMIM:Sialorrhea]
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]
Drooling (in some patients) [OMIM:Drooling (in some patients)]
Hypersalivation [OMIM:Hypersalivation]
Drooling [MedDRA:10013642]
Quality:
Cross references:
HPO:0003781 "Excessive salivation" [Orphanet:27060]
Orphanet:27060 "Hypersialorrhea" [Orphanet:27060]
OMIM: "Drooling" [OMIM:Drooling]
OMIM: "Sialorrhea" [OMIM:Sialorrhea]
OMIM: "Drooling (in some patients)" [OMIM:Drooling (in some patients)]
OMIM: "Hypersalivation" [OMIM:Hypersalivation]
UMLS:C0013132 "Drooling" [HPO:0002307]
UMLS:C0037036 "Sialorrhea" [Orphanet:27060]
Is a (Direct Parents):
Orphanet Functional anomalies of the digestive system
MedDRA Oral dryness and saliva altered
HPO         Excessive salivation
HPO         Behavioral abnormality
MedDRA Neurological signs and symptoms NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Behavioral abnormality(HPO:0000708)
                   Drooling(HPO:0002307)
       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)
                            Drooling(HPO:0002307)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Salivary gland conditions(MedDRA:10039404)
       Oral dryness and saliva altered(MedDRA:10030975)
          Drooling(HPO:0002307)
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Neurological signs and symptoms NEC(MedDRA:10029306)
          Drooling(HPO:0002307)
Database Frequency: 43 / 7739
Resource:

All diseases associated with this symptom:

6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (OMIM:205100)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Angelman syndrome (Orphanet:72)
Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
Autosomal recessive spastic paraplegia type 20 (Orphanet:101000)
Bilateral frontal polymicrogyria (Orphanet:208444)
Carpenter-Waziri syndrome (Orphanet:93973)
Choreoacanthocytosis (Orphanet:2388)
Christianson syndrome (Orphanet:85278)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Dihydropteridine reductase deficiency (Orphanet:226)
Dopa-responsive dystonia due to sepiapterin reductase deficiency (Orphanet:70594)
GTP cyclohydrolase I deficiency (Orphanet:2102)
Holmes-Gang syndrome (Orphanet:93970)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Juberg-Marsidi syndrome (Orphanet:93972)
Juvenile amyotrophic lateral sclerosis (Orphanet:300605)
LUBS X-LINKED MENTAL RETARDATION SYNDROME (OMIM:300260)
Lethal ataxia with deafness and optic atrophy (Orphanet:1187)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 23 (OMIM:615761)
MENTAL RETARDATION, X-LINKED 30 (OMIM:300558)
Mowat-Wilson syndrome (Orphanet:2152)
ORAL SENSIBILITY, DISTURBANCE OF (OMIM:258800)
Odontoleukodystrophy (Orphanet:77295)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Polymicrogyria due to TUBB2B mutation (Orphanet:300573)
Pyruvate dehydrogenase E2 deficiency (Orphanet:79244)
Pyruvate dehydrogenase deficiency (Orphanet:765)
Qazi-Markouizos syndrome (Orphanet:3010)
RETT SYNDROME, CONGENITAL VARIANT (OMIM:613454)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE (OMIM:612936)
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE (OMIM:613744)
Sanfilippo syndrome type D (Orphanet:79272)
Severe intellectual deficit and progressive spastic paraplegia (Orphanet:280763)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Wilson disease (Orphanet:905)
Worster-Drought syndrome (Orphanet:3465)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)