Skin tags
Symptom Information:
Symptom ID: | HPO:0010609 | ||||
Synonyms: |
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Quality: | |||||
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) Localized skin lesion(HPO:0011355) Skin tags(HPO:0010609) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Aicardi syndrome | (Orphanet:50) |
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Birt-Hogg-Dube syndrome | (Orphanet:122) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cowden syndrome | (Orphanet:201) |
Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
GAPO syndrome | (Orphanet:2067) |
Gorlin syndrome | (Orphanet:377) |
OPITZ-KAVEGGIA SYNDROME | (OMIM:305450) |
Pai syndrome | (Orphanet:1993) |
Tuberous sclerosis | (Orphanet:805) |