Sclerodactyly

Symptom Information:

Symptom ID: HPO:0011838
Synonyms:
Sclerodactyly [OMIM:Sclerodactyly]
Quality:
Cross references:
OMIM: "Sclerodactyly" [OMIM:Sclerodactyly]
Is a (Direct Parents):
HPO         Thickened skin
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)
                      Sclerodactyly(HPO:0011838)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
CREST syndrome (Orphanet:90290)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Limited systemic sclerosis (Orphanet:220407)
Pediatric systemic sclerosis (Orphanet:93567)
Reynolds syndrome (Orphanet:779)
Systemic sclerosis (Orphanet:90291)