Congenital palmoplantar keratodermia

Symptom Information:

Symptom ID: HPO:0007597
Synonyms:
Congenital palmoplantar keratodermia [OMIM:Congenital palmoplantar keratodermia]
Quality:
Cross references:
OMIM: "Congenital palmoplantar keratodermia" [OMIM:Congenital palmoplantar keratodermia]
Is a (Direct Parents):
HPO         Palmoplantar keratoderma
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)
                      Epidermal thickening(HPO:0011368)
                         Hyperkeratosis(HPO:0000962)
                            Palmoplantar keratoderma(HPO:0000982)
                               Congenital palmoplantar keratodermia(HPO:0007597)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Palmoplantar keratoderma-sclerodactyly syndrome (Orphanet:384)