Xerostomia

Symptom Information:

Symptom ID: HPO:0000217
Synonyms:
Dry mouth [HPO:0000217]
Reduced salivation [HPO:0000217]
Reduced salivation [Orphanet:27090]
Aptyalism (disorder) [Orphanet:9760]
Hyposecretion of salivary gland (disorder) [Orphanet:9760]
Reduced salivation (finding) [Orphanet:27090]
Xerostomia [Orphanet:9760]
Dry mouth [OMIM:Dry mouth]
Xerostomia [OMIM:Xerostomia]
Mouth dryness/xerostomia [Orphanet:9760]
Hyposialorrhea [Orphanet:27090]
Dry mouth [Orphanet:9760]
Aptyalism [Orphanet:9760]
Dry mouth [MedDRA:10013781]
Dryness oral [MedDRA:10013781]
Mouth became dry [MedDRA:10013781]
Mouth dry [MedDRA:10013781]
Mouth feeling dry [MedDRA:10013781]
Oral dryness [MedDRA:10013781]
Xerostomia [MedDRA:10013781]
Mouth dry aggravated [MedDRA:10013781]
Mouth puckered [MedDRA:10013781]
Mouth tight [MedDRA:10013781]
Mouth drawn [MedDRA:10013781]
Mouth shriveled [MedDRA:10013781]
Gingival dryness [MedDRA:10013781]
Aptyalism [MedDRA:10003068]
Saliva decreased [MedDRA:10003068]
Salivary hyposecretion [MedDRA:10003068]
Aptyalia [MedDRA:10003068]
Asialia [MedDRA:10003068]
Decreased saliva [OMIM:Decreased saliva]
Quality:
Cross references:
Orphanet:9760 "Mouth dryness/xerostomia" [Orphanet:9760]
Orphanet:27090 "Hyposialorrhea" [Orphanet:27090]
OMIM: "Dry mouth" [OMIM:Dry mouth]
OMIM: "Xerostomia" [OMIM:Xerostomia]
OMIM: "Decreased saliva" [OMIM:Decreased saliva]
UMLS:C0043352 "Xerostomia" [HPO:0000217]
UMLS:C0043352 "Xerostomia" [Orphanet:9760]
UMLS:C0576990 "Reduced salivation" [Orphanet:27090]
Is a (Direct Parents):
Orphanet Functional anomalies of the digestive system
HPO         Abnormality of salivation
Orphanet Abnormality of the mouth
MedDRA Oral dryness and saliva altered
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)
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)