Keloids

Symptom Information:

Symptom ID: HPO:0010562
Synonyms:
Cheloid [Orphanet:23120]
Keloid [HPO:0010562]
Keloid scar (disorder) [Orphanet:23120]
Keloid (morphologic abnormality) [Orphanet:23120]
Keloid [Orphanet:23120]
Keloids [OMIM:Keloids]
Abnormal scarring/cheloids/hypertrophic scars [Orphanet:23120]
Keloid scar [HPO:0010562]
Keloid scar [Orphanet:23120]
Keloid scar [MedDRA:10023330]
Keloid [MedDRA:10023330]
Keloid [OMIM:Keloid]
Skin scarring anomaly [Orphanet:23120]
Hypertrophic scar [MedDRA:10020879]
Hypertrophic scar (disorder) [Orphanet:23120]
Cicatrix, Hypertrophic [Orphanet:23120]
Quality:
Cross references:
Orphanet:23120 "Abnormal scarring/cheloids/hypertrophic scars" [Orphanet:23120]
OMIM: "Keloids" [OMIM:Keloids]
OMIM: "Keloid" [OMIM:Keloid]
UMLS:C0022548 "Keloids" [HPO:0010562]
UMLS:C0022548 "Keloid" [Orphanet:23120]
UMLS:C0162810 "Cicatrix, Hypertrophic" [Orphanet:23120]
Is a (Direct Parents):
Orphanet Abnormality of the skin
MedDRA Skin dystrophies
HPO         Atypical scarring of skin
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Scarring(HPO:0100699)
             Atypical scarring of skin(HPO:0000987)
                Keloids(HPO:0010562)
       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)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Skin dystrophies(MedDRA:10040837)
          Keloids(HPO:0010562)
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)