Congenital ichthyosiform erythroderma

Symptom Information:

Symptom ID: HPO:0007431
Synonyms:
Congenital ichthyosis [HPO:0007431]
Ichthyosis, congenital [HPO:0007431]
Congenital ichthyosiform erythroderma [OMIM:Congenital ichthyosiform erythroderma]
Congenital ichthyosis [OMIM:Congenital ichthyosis]
Ichthyosis, congenital [OMIM:Ichthyosis, congenital]
Quality:
Cross references:
OMIM: "Congenital ichthyosiform erythroderma" [OMIM:Congenital ichthyosiform erythroderma]
OMIM: "Congenital ichthyosis" [OMIM:Congenital ichthyosis]
OMIM: "Ichthyosis, congenital" [OMIM:Ichthyosis, congenital]
Is a (Direct Parents):
HPO         Ichthyosis
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)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Bathing suit ichthyosis (Orphanet:100976)
CHILD syndrome (Orphanet:139)
Congenital cataract - ichthyosis (Orphanet:1376)
Gaucher disease type 2 (Orphanet:77260)
Harlequin ichthyosis (Orphanet:457)
ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED (OMIM:308200)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 10 (OMIM:615024)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 4A (OMIM:601277)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 9 (OMIM:615023)
ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA (OMIM:242550)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
NEUTROPHIL MIGRATION (OMIM:162820)
SJOGREN-LARSSON-LIKE ICHTHYOSIS WITHOUT CNS OR EYE INVOLVEMENT (OMIM:270220)
Self-healing collodion baby (Orphanet:281122)
Syndromic X-linked ichthyosis (Orphanet:281090)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)