Porokeratosis

Symptom Information:

Symptom ID: HPO:0200044
Synonyms:
Porokeratosis [OMIM:Porokeratosis]
Porokeratosis [MedDRA:10036175]
Quality:
Cross references:
OMIM: "Porokeratosis" [OMIM:Porokeratosis]
Is a (Direct Parents):
MedDRA Skin and subcutaneous tissue disorders congenital NEC
HPO         Epidermal thickening
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)
                         Porokeratosis(HPO:0200044)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Skin and subcutaneous tissue disorders congenital(MedDRA:10040789)
       Skin and subcutaneous tissue disorders congenital NEC(MedDRA:10040834)
          Porokeratosis(HPO:0200044)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
Disseminated superficial actinic porokeratosis (Orphanet:79152)
POROKERATOSIS 3, DISSEMINATED SUPERFICIAL ACTINIC TYPE (OMIM:175900)
POROKERATOSIS 6, DISSEMINATED SUPERFICIAL ACTINIC TYPE (OMIM:612353)
POROKERATOSIS 7, DISSEMINATED SUPERFICIAL ACTINIC TYPE (OMIM:614714)
POROKERATOSIS 8, DISSEMINATED SUPERFICIAL ACTINIC TYPE (OMIM:616063)
Porokeratosis of Mibelli (Orphanet:735)
Porokeratosis plantaris palmaris et disseminata (Orphanet:737)
Primary localized amyloidosis (Orphanet:314709)
Punctate palmoplantar keratoderma type 2 (Orphanet:79502)