Congenital bullous ichthyosiform erythroderma

Symptom Information:

Symptom ID: HPO:0007475
Synonyms:
Bullous congenital ichthyosiform erythroderma [HPO:0007475]
Epidermolytic hyperkeratosis [HPO:0007475]
Quality:
Cross references:
Is a (Direct Parents):
HPO         Congenital ichthyosiform erythroderma
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)
                         Ichthyosis(HPO:0008064)
                            Congenital ichthyosiform erythroderma(HPO:0007431)
                               Congenital bullous ichthyosiform erythroderma(HPO:0007475)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

Annular epidermolytic ichthyosis (Orphanet:281139)
Ectodermal dysplasia - cutaneous syndactyly syndrome (Orphanet:247827)
Superficial epidermolytic ichthyosis (Orphanet:455)
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome (Orphanet:65282)