Congenital nonbullous ichthyosiform erythroderma

Symptom Information:

Symptom ID: HPO:0007479
Synonyms:
Collodion baby [HPO:0007479]
Congenital lamellar ichthyosis [HPO:0007479]
Congenital non-bullous ichthyosis [HPO:0007479]
Ichthyosis lammellaris [HPO:0007479]
Ichthyosis, congenital, nonblistering [HPO:0007479]
Nonbullous congenital ichthyosiform erythroderma [HPO:0007479]
Nonbullous congenital ichthyosis [HPO:0007479]
Collodion baby [OMIM:Collodion baby]
Congenital lamellar ichthyosis [OMIM:Congenital lamellar ichthyosis]
Congenital non-bullous ichthyosis [OMIM:Congenital non-bullous ichthyosis]
Ichthyosis, congenital, nonblistering [OMIM:Ichthyosis, congenital, nonblistering]
Nonbullous congenital ichthyosiform erythroderma [OMIM:Nonbullous congenital ichthyosiform erythroderma]
Collodion baby [MedDRA:10009926]
Quality:
Cross references:
OMIM: "Collodion baby" [OMIM:Collodion baby]
OMIM: "Congenital lamellar ichthyosis" [OMIM:Congenital lamellar ichthyosis]
OMIM: "Congenital non-bullous ichthyosis" [OMIM:Congenital non-bullous ichthyosis]
OMIM: "Ichthyosis, congenital, nonblistering" [OMIM:Ichthyosis, congenital, nonblistering]
OMIM: "Nonbullous congenital ichthyosiform erythroderma" [OMIM:Nonbullous congenital ichthyosiform erythroderma]
Is a (Direct Parents):
HPO         Congenital ichthyosiform erythroderma
MedDRA Newborn complications NEC
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 nonbullous ichthyosiform erythroderma(HPO:0007479)
MedDRA:
Pregnancy, puerperium and perinatal conditions(MedDRA:10036585)
    Neonatal and perinatal conditions(MedDRA:10028920)
       Newborn complications NEC(MedDRA:10010168)
          Congenital nonbullous ichthyosiform erythroderma(HPO:0007479)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Dorfman-Chanarin disease (Orphanet:98907)
Fetal Gaucher disease (Orphanet:85212)
Gaucher disease type 2 (Orphanet:77260)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 3 (OMIM:606545)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5 (OMIM:604777)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 (OMIM:612281)
Ichthyosis - intellectual deficit - dwarfism - renal impairment (Orphanet:2278)
KETOADIPICACIDURIA (OMIM:245130)
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome (Orphanet:281201)
Lamellar ichthyosis (Orphanet:313)
Netherton syndrome (Orphanet:634)
Self-healing collodion baby (Orphanet:281122)
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (OMIM:601675)