FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

7731005: syndroom van autosomaal dominante anhidrotische ectodermale dysplasie (aandoening)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
13786011 Autosomal dominant hypohidrotic ectodermal dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
13787019 Rapp-Hodgkin ectodermal dysplasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
503512017 Anhidrotic ectodermal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503513010 Rapp-Hodgkin type of ectodermal dysplasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
503515015 Anhidrotic ectodermal dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503516019 Hypohidrotic ectodermal dysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
818127016 Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6342301000146113 syndroom van Rapp-Hodgkin nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6342331000146115 Rapp-Hodgkin-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7110081000146117 syndroom van autosomaal dominante anhidrotische ectodermale dysplasie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
7110091000146115 syndroom van autosomaal dominante anhidrotische ectodermale dysplasie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Hereditary disorder of the integument true Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Ectodermal dysplasia with hair-tooth-nail-sweating defect true Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Skin structure true Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence Congenital false Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology congenitale anomalie (afwijkende morfologie) false Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Skin structure false Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence Congenital true Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Skin structure false Inferred relationship Some 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Skin structure false Inferred relationship Some 4
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence Congenital true Inferred relationship Some 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Skin lesion true Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Ectoderm structure false Inferred relationship Some 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology Dysplasia false Inferred relationship Some 4
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology congenitale dysplasie (afwijkende morfologie) false Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Ectoderm structure true Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology Dysplasia true Inferred relationship Some 2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence Congenital true Inferred relationship Some 5
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 5
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Nail unit structure true Inferred relationship Some 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Hair structure (body structure) true Inferred relationship Some 5
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Occurrence Congenital true Inferred relationship Some 4
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site Tooth structure true Inferred relationship Some 4
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Genetic disorder of nail (disorder) true Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Has interpretation Abnormal true Inferred relationship Some 6
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Interprets Sweating, function (observable entity) true Inferred relationship Some 6
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Is a Hereditary disorder of tooth true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypohidrotic X-linked ectodermal dysplasia Is a False Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Inferred relationship Some

This concept is not in any reference sets

Back to Start