Lip telangiectasia

Symptom Information:

Symptom ID: HPO:0000214
Synonyms:
Lip telangiectases [HPO:0000214]
TELANGIECTASIA OF THE LIPS [HPO:0000214]
Lip telangiectases [OMIM:Lip telangiectases]
Telangiectasia of the lips [OMIM:Telangiectasia of the lips]
Quality:
Cross references:
OMIM: "Lip telangiectases" [OMIM:Lip telangiectases]
OMIM: "Telangiectasia of the lips" [OMIM:Telangiectasia of the lips]
Is a (Direct Parents):
HPO         Oral cavity telangiectasia
HPO         Abnormality of the lip
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)
                      Lip telangiectasia(HPO:0000214)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of oral mucosa(HPO:0011830)
                         Oral cavity telangiectasia(HPO:0000228)
                            Lip telangiectasia(HPO:0000214)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Vascular skin abnormality(HPO:0011276)
                   Telangiectasia(HPO:0001009)
                      Mucosal telangiectasiae(HPO:0100579)
                         Oral cavity telangiectasia(HPO:0000228)
                            Lip telangiectasia(HPO:0000214)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Reynolds syndrome (Orphanet:779)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 (OMIM:610655)