Mucosal telangiectasiae
Symptom Information:
Symptom ID: | HPO:0100579 | ||||
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 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) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Ataxia-telangiectasia | (Orphanet:100) |
CREST syndrome | (Orphanet:90290) |
Cowden syndrome | (Orphanet:201) |
Fabry disease | (Orphanet:324) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
Juvenile dermatomyositis | (Orphanet:93672) |
Limited cutaneous systemic sclerosis | (Orphanet:220402) |
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications | (Orphanet:3018) |
Reynolds syndrome | (Orphanet:779) |
Scleroderma | (Orphanet:801) |