Cheilitis

Symptom Information:

Symptom ID: HPO:0100825
Synonyms:
Cheilitis (disorder) [Orphanet:9720]
Cheilitis [Orphanet:9720]
Oral mucosa disease/cheilitis [Orphanet:9720]
Cheilitis [MedDRA:10008417]
Angular cheilitis [MedDRA:10008417]
Angular stomatitis [MedDRA:10008417]
Lip redness [MedDRA:10008417]
Desquamative cheilitis [MedDRA:10008417]
Rash lips [MedDRA:10008417]
Irritation lips [MedDRA:10008417]
Raw lips [MedDRA:10008417]
Redness corner of mouth [MedDRA:10008417]
Inflammation lips [MedDRA:10008417]
Soreness corner mouth [MedDRA:10008417]
Sores lip [MedDRA:10008417]
Perleche [MedDRA:10008417]
Angular cheilosis [MedDRA:10008417]
Angular cheilitis [OMIM:Angular cheilitis]
Quality:
Cross references:
Orphanet:9720 "Oral mucosa disease/cheilitis" [Orphanet:9720]
OMIM: "Angular cheilitis" [OMIM:Angular cheilitis]
UMLS:C0007971 "Cheilitis" [HPO:0100825]
UMLS:C0007971 "Cheilitis" [Orphanet:9720]
Is a (Direct Parents):
Orphanet Abnormality of the mouth
HPO         Abnormality of the lip
MedDRA Oral soft tissue disorders NEC
HPO         Angular cheilitis
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)
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)