Recurrent aphthous stomatitis

Symptom Information:

Symptom ID: HPO:0011107
Synonyms:
Aphthous stomatitis [HPO:0011107]
aphthous ulcers [HPO:0011107]
Buccal aphthous ulcers [HPO:0011107]
Canker sore [HPO:0011107]
Aphthous stomatitis [OMIM:Aphthous stomatitis]
Aphthous ulcers [OMIM:Aphthous ulcers]
Recurrent aphthous stomatitis [OMIM:Recurrent aphthous stomatitis]
Aphthous ulcers (lips, gingiva, buccal mucosa) [OMIM:Aphthous ulcers (lips, gingiva, buccal mucosa)]
Aphthous stomatitis [MedDRA:10002958]
Quality:
Cross references:
OMIM: "Aphthous stomatitis" [OMIM:Aphthous stomatitis]
OMIM: "Aphthous ulcers" [OMIM:Aphthous ulcers]
OMIM: "Recurrent aphthous stomatitis" [OMIM:Recurrent aphthous stomatitis]
OMIM: "Aphthous ulcers (lips, gingiva, buccal mucosa)" [OMIM:Aphthous ulcers (lips, gingiva, buccal mucosa)]
Is a (Direct Parents):
HPO         Stomatitis
MedDRA Stomatitis and ulceration
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 oral mucosa(HPO:0011830)
                         Stomatitis(HPO:0010280)
                            Recurrent aphthous stomatitis(HPO:0011107)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Oral soft tissue conditions(MedDRA:10031013)
       Stomatitis and ulceration(MedDRA:10042129)
          Recurrent aphthous stomatitis(HPO:0011107)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive lymphoproliferative disease (Orphanet:238505)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Barth syndrome (Orphanet:111)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
Combined immunodeficiency due to CRAC channel dysfunction (Orphanet:169090)
Combined immunodeficiency due to ORAI1 deficiency (Orphanet:317428)
Cyclic neutropenia (Orphanet:2686)
GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-POSITIVE,TYPE III (OMIM:613960)
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES (OMIM:615966)
INFLAMMATORY BOWEL DISEASE 1 (OMIM:266600)
Muckle-Wells syndrome (Orphanet:575)
NLRP12-associated hereditary periodic fever syndrome (Orphanet:247868)
Polyarteritis nodosa, childhood-onset (OMIM:615688)