FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

722391005: Congenital lethal erythroderma (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3331824010 Congenital lethal erythroderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331825011 Congenital lethal erythroderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402915018 A rare skin disorder characterized by erythrodermic, peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhea, failure to thrive and severe hypoalbuminemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402916017 A rare skin disorder characterised by erythrodermic, peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhoea, failure to thrive and severe hypoalbuminaemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331824010 Congenital lethal erythroderma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331824010 Congenital lethal erythroderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331825011 Congenital lethal erythroderma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3331825011 Congenital lethal erythroderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3331826012 A rare skin disorder characterized by erythrodermic peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhea, failure to thrive and severe hypoalbuminemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331827015 A rare skin disorder characterised by erythrodermic peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhoea, failure to thrive and severe hypoalbuminaemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402915018 A rare skin disorder characterized by erythrodermic, peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhea, failure to thrive and severe hypoalbuminemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402916017 A rare skin disorder characterised by erythrodermic, peeling skin from birth with no obvious nail or hair-shaft abnormalities and other associated anomalies including diarrhoea, failure to thrive and severe hypoalbuminaemia resistant to correction by enteral or intravenous supplementation. An autosomal recessive mode of inheritance is highly probable. The prognosis is poor and infants die in the first months of life. There have been no further descriptions in the literature since 1992. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3381721001000118 Erythrodermie, kongenitale letale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
976351000172110 erythrodermie congénitale létale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
976351000172110 erythrodermie congénitale létale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3381721001000118 Erythrodermie, kongenitale letale de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital lethal erythroderma (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital lethal erythroderma (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital lethal erythroderma (disorder) Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital lethal erythroderma (disorder) Is a Erythroderma (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital lethal erythroderma (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital lethal erythroderma (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital lethal erythroderma (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital lethal erythroderma (disorder) Associated morphology Diffuse inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital lethal erythroderma (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital lethal erythroderma (disorder) Associated morphology Erythema false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital lethal erythroderma (disorder) Is a Inflammatory dermatosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital lethal erythroderma (disorder) Is a Inflammation of specific body organs false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital lethal erythroderma (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital lethal erythroderma (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital lethal erythroderma (disorder) Associated morphology Exfoliative erythema true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital lethal erythroderma (disorder) Is a Disorder involving the integument of fetus OR newborn true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start