About: Congenital ichthyosiform erythroderma

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Congenital ichthyosiform erythroderma (CIE), also known as nonbullous congenital ichthyosiform erythroderma, is a rare type of the ichthyosis family of skin diseases which occurs in 1 in 200,000 to 300,000 births. CIE comes under the umbrella term autosomal recessive congenital ichthyosis (ARCI), which include non-syndromic congenital ichthyoses such as harlequin ichthyosis and lamellar ichthyosis.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalRecessiveDisorders yago:WikicatCongenitalDisorders yago:Abnormality114501726 yago:Abstraction100002137 yago:Anomaly114505821 yago:Attribute100024264 yago:BirthDefect114465048 yago:Condition113920835 yago:Defect114464005 yago:Disease114070360 yago:Disorder114052403 yago:IllHealth114052046 yago:Illness114061805 yago:Imperfection114462666 yago:PathologicalState114051917 yago:PhysicalCondition114034177 disease yago:State100024720 umbel-rc:AilmentCondition
rdfs:label	Kongenitale ichthyosiforme Erythrodermie (de) Congenital ichthyosiform erythroderma (en) Eritrodermia ittiosiforme congenita (it)
rdfs:comment	Congenital ichthyosiform erythroderma (CIE), also known as nonbullous congenital ichthyosiform erythroderma, is a rare type of the ichthyosis family of skin diseases which occurs in 1 in 200,000 to 300,000 births. CIE comes under the umbrella term autosomal recessive congenital ichthyosis (ARCI), which include non-syndromic congenital ichthyoses such as harlequin ichthyosis and lamellar ichthyosis. (en) Per eritrodermia ittiosiforme congenita (o bollosa congenita) in campo medico, si intende una forma di genodermatosi con carattere autosomico dominante. (it) Die Kongenitale ichthyosiforme Erythrodermie (CIE) ist eine sehr seltene, zu den autosomal-rezessiven kongenitalen Ichthyosen (ARCI) gehörende angeborene Hauterkrankung mit einer Kombination von Rötung der Haut des ganzen Körpers (Erythrodermie) und feinen, weißen Schuppen (Ichthyose). Die Erkrankung kann als Variante der lamellären Ichthyose angesehen werden. Synonyme sind: Ichthyose, erythrodermische; englisch Congenital non-bullous ichthyosiform erythroderma (de)
foaf:name	Congenital Ichthyosiform Erythroderma (en)
name	Congenital Ichthyosiform Erythroderma (en)
dcterms:subject	Autosomal recessive disorders Genodermatoses Rare diseases
Wikipage page ID	20331838 (xsd:integer)
Wikipage revision ID	1084492267 (xsd:integer)
Link from a Wikipage to another Wikipage	Hyperkeratosis Alopecia Autosomal recessive disorders Collodion baby Ichthyosis Lamellar ichthyosis Genodermatoses Rare diseases ALOX12B ALOXE3 Ectropion List of cutaneous conditions Harlequin Ichthyosis TGM1
Link from a Wikipage to an external page	https://www.ncbi.nlm.nih.gov/books/NBK1420/
sameAs	Congenital ichthyosiform erythroderma Congenital ichthyosiform erythroderma Congenital ichthyosiform erythroderma Congenital ichthyosiform erythroderma Congenital ichthyosiform erythroderma Congenital ichthyosiform erythroderma
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Cn dbt:Empty_section dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Rp dbt:Npsn dbt:Congenital_malformations_and_deformations_of_integument
DiseasesDB	33314 (xsd:integer)
ICD	757.100000 (xsd:double) (en) Q80.2 (en)
MeshID	D016113 (en)
OMIM	242100 (xsd:integer)
synonyms	Nonbullous congenital ichthyosiform erythroderma (en)
has abstract	Die Kongenitale ichthyosiforme Erythrodermie (CIE) ist eine sehr seltene, zu den autosomal-rezessiven kongenitalen Ichthyosen (ARCI) gehörende angeborene Hauterkrankung mit einer Kombination von Rötung der Haut des ganzen Körpers (Erythrodermie) und feinen, weißen Schuppen (Ichthyose). Die Erkrankung kann als Variante der lamellären Ichthyose angesehen werden. Synonyme sind: Ichthyose, erythrodermische; englisch Congenital non-bullous ichthyosiform erythroderma Die Erkrankung ist als nicht-bullöse Form von der autosomal-dominant vererbten Epidermolytischen Ichthyose (Bullöse kongenitale ichthyosiforme Erythrodermie Brocq) abzugrenzen. (de) Congenital ichthyosiform erythroderma (CIE), also known as nonbullous congenital ichthyosiform erythroderma, is a rare type of the ichthyosis family of skin diseases which occurs in 1 in 200,000 to 300,000 births. CIE comes under the umbrella term autosomal recessive congenital ichthyosis (ARCI), which include non-syndromic congenital ichthyoses such as harlequin ichthyosis and lamellar ichthyosis. (en) Per eritrodermia ittiosiforme congenita (o bollosa congenita) in campo medico, si intende una forma di genodermatosi con carattere autosomico dominante. (it)
gold:hypernym	Type
ICD9	757.1
MeSH ID	D016113
prov:wasDerivedFrom	wikipedia-en:Congenital_ichthyosiform_erythroderma?oldid=1084492267&ns=0
page length (characters) of wiki page	6448 (xsd:nonNegativeInteger)
DiseasesDB	33314
ICD10	Q80.2
OMIM id	242100 (xsd:integer)
foaf:isPrimaryTopicOf	wikipedia-en:Congenital_ichthyosiform_erythroderma
is Link from a Wikipage to another Wikipage of	Carly Findlay Non-bullous congenital ichthyosiform erythroderma 12-Hydroxyeicosatetraenoic acid Ichthyosis Lipoxygenase Harlequin-type ichthyosis ALOX12B ALOXE3 Eclabium CIE CYP4F22 NIPAL4 Nonbullous congenital ichthyosiform erythroderma Congenital ichthyosiform erythrodema Congenital ichtyosiform erythroderma
is Wikipage redirect of	Non-bullous congenital ichthyosiform erythroderma Nonbullous congenital ichthyosiform erythroderma

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