Xerostomia
Symptom Information:
Symptom ID: | HPO:0000217 | ||||||||||||||||||||||||||||||||
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) Xerostomia(HPO:0000217) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Salivary gland conditions(MedDRA:10039404) Oral dryness and saliva altered(MedDRA:10030975) Xerostomia(HPO:0000217) |
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Database Frequency: | 35 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Adiposis dolorosa | (Orphanet:36397) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Antisynthetase syndrome | (Orphanet:81) |
Aplasia of lacrimal and salivary glands | (Orphanet:86815) |
Blau syndrome | (Orphanet:90340) |
Botulism | (Orphanet:1267) |
Cholera | (Orphanet:173) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Diffuse cutaneous systemic sclerosis | (Orphanet:220393) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Fabry disease | (Orphanet:324) |
Familial esophageal achalasia | (Orphanet:99723) |
Foodborne botulism | (Orphanet:228371) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Idiopathic achalasia | (Orphanet:930) |
Infant botulism | (Orphanet:178478) |
Inhalational botulism | (Orphanet:254504) |
Intestinal botulism | (Orphanet:178481) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Limited systemic sclerosis | (Orphanet:220407) |
MELAS | (Orphanet:550) |
Mixed connective tissue disease | (Orphanet:809) |
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX | (OMIM:260480) |
Primary erythermalgia | (Orphanet:90026) |
Prune belly syndrome | (Orphanet:2970) |
Reynolds syndrome | (Orphanet:779) |
SJOGREN SYNDROME | (OMIM:270150) |
Scleroderma | (Orphanet:801) |
Sodium channelopathy-related small fiber neuropathy | (Orphanet:306577) |
Systemic sclerosis | (Orphanet:90291) |
Thymoma | (Orphanet:99867) |