Recurrent aphthous stomatitis
Symptom Information:
Symptom ID: | HPO:0011107 | |||||||||
Synonyms: |
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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 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) |
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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) |