Scleroderma

Symptom Information:

Symptom ID: HPO:0100324
Synonyms:
Progressive systemic scleroderma [HPO:0100324]
Pseudoscleroderma [HPO:0100324]
Progressive systemic scleroderma [OMIM:Progressive systemic scleroderma]
Pseudoscleroderma [OMIM:Pseudoscleroderma]
Scleroderma [OMIM:Scleroderma]
Scleroderma [MedDRA:10039710]
Quality:
Cross references:
OMIM: "Progressive systemic scleroderma" [OMIM:Progressive systemic scleroderma]
OMIM: "Pseudoscleroderma" [OMIM:Pseudoscleroderma]
OMIM: "Scleroderma" [OMIM:Scleroderma]
UMLS:C1274865 "Pseudoscleroderma" [HPO:0100324]
Is a (Direct Parents):
HPO         Thickened skin
MedDRA Scleroderma and associated disorders
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)
                Abnormality of skin morphology(HPO:0011121)
                   Thickened skin(HPO:0001072)
                      Scleroderma(HPO:0100324)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Autoimmunity(HPO:0002960)
       Scleroderma and associated disorders(MedDRA:10039711)
          Scleroderma(HPO:0100324)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

CREST syndrome (Orphanet:90290)
Congenital erythropoietic porphyria (Orphanet:79277)
Hepatoerythropoietic porphyria (Orphanet:95159)
Maternal hyperphenylalaninemia (Orphanet:2209)
Phenylketonuria (Orphanet:716)
Systemic sclerosis (Orphanet:90291)