Keloids
Symptom Information:
Symptom ID: | HPO:0010562 | ||||||||||||||||
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) Atypical scarring of skin(HPO:0000987) Keloids(HPO:0010562) Abnormality of connective tissue(HPO:0003549) Scarring(HPO:0100699) Atypical scarring of skin(HPO:0000987) Keloids(HPO:0010562) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Cornification and dystrophic skin disorders(MedDRA:10011063) Skin dystrophies(MedDRA:10040837) Keloids(HPO:0010562) |
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Database Frequency: | 11 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
APC-related attenuated familial adenomatous polyposis | (Orphanet:247806) |
Attenuated familial adenomatous polyposis | (Orphanet:220460) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
Familial adenomatous polyposis | (Orphanet:733) |
Gardner syndrome | (Orphanet:79665) |
KELOID FORMATION | (OMIM:148100) |
Menkes disease | (Orphanet:565) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Turcot syndrome with polyposis | (Orphanet:99818) |