Drooling
Symptom Information:
Symptom ID: | HPO:0002307 | |||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) Drooling(HPO:0002307) 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) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Neurological signs and symptoms NEC(MedDRA:10029306) Drooling(HPO:0002307) Gastrointestinal disorders(MedDRA:10017947) Salivary gland conditions(MedDRA:10039404) Oral dryness and saliva altered(MedDRA:10030975) Drooling(HPO:0002307) |
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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) |