Congenital palmoplantar keratosis

Symptom Information:

Symptom ID: HPO:0007545
Synonyms:
Congenital palmoplantar keratosis [OMIM:Congenital palmoplantar keratosis]
Quality:
Cross references:
OMIM: "Congenital palmoplantar keratosis" [OMIM:Congenital palmoplantar keratosis]
Is a (Direct Parents):
HPO         Palmoplantar hyperkeratosis
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)
                            Plantar hyperkeratosis(HPO:0007556)
                               Palmoplantar hyperkeratosis(HPO:0000972)
                                  Congenital palmoplantar keratosis(HPO:0007545)
                            Palmar hyperkeratosis(HPO:0010765)
                               Palmoplantar hyperkeratosis(HPO:0000972)
                                  Congenital palmoplantar keratosis(HPO:0007545)
             Regional abnormality of skin(HPO:0011356)
                Abnormality of the plantar skin of foot(HPO:0100872)
                   Palmoplantar hyperkeratosis(HPO:0000972)
                      Congenital palmoplantar keratosis(HPO:0007545)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal appendicular skeleton morphology(HPO:0011844)
                Abnormality of limb bone morphology(HPO:0002813)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Abnormality of the palm(HPO:0100871)
                            Palmoplantar hyperkeratosis(HPO:0000972)
                               Congenital palmoplantar keratosis(HPO:0007545)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Haim-Munk syndrome (Orphanet:2342)