Cheilitis
Symptom Information:
Symptom ID: | HPO:0100825 | ||||||||||||||||||
Synonyms: |
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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 lip(HPO:0000159) Cheilitis(HPO:0100825) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Oral soft tissue conditions(MedDRA:10031013) Oral soft tissue disorders NEC(MedDRA:10031015) Cheilitis(HPO:0100825) |
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Database Frequency: | 20 / 7739 | ||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY | (OMIM:174770) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Cheilitis glandularis | (Orphanet:1221) |
Chronic mucocutaneous candidiasis | (Orphanet:1334) |
Dystrophic epidermolysis bullosa | (Orphanet:303) |
Generalized dominant dystrophic epidermolysis bullosa | (Orphanet:231568) |
Hereditary folate malabsorption | (Orphanet:90045) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Kawasaki disease | (Orphanet:2331) |
Kindler syndrome | (Orphanet:2908) |
Melkersson-Rosenthal syndrome | (Orphanet:2483) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oral erosive lichen | (Orphanet:31142) |
Oral submucous fibrosis | (Orphanet:357154) |
PANCREATITIS, SCLEROSING CHOLANGITIS, AND SICCA COMPLEX | (OMIM:260480) |
Pseudo-pelade of Brocq | (Orphanet:129) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Scleroderma | (Orphanet:801) |
Transient bullous dermolysis of the newborn | (Orphanet:79411) |