FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

707273001: Autosomal dominant dyskeratosis congenita (disorder)


Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3029387019 Autosomal dominant dyskeratosis congenita (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3029520015 Autosomal dominant dyskeratosis congenita en Synonym Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant dyskeratosis congenita Pathological process Pathological developmental process true Inferred relationship Some 1
Autosomal dominant dyskeratosis congenita Occurrence Congenital true Inferred relationship Some 2
Autosomal dominant dyskeratosis congenita Pathological process Pathological developmental process true Inferred relationship Some 2
Autosomal dominant dyskeratosis congenita Finding site Ectoderm structure true Inferred relationship Some 2
Autosomal dominant dyskeratosis congenita Associated morphology Dysplasia true Inferred relationship Some 2
Autosomal dominant dyskeratosis congenita Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant dyskeratosis congenita Is a Dyskeratosis congenita true Inferred relationship Some
Autosomal dominant dyskeratosis congenita Associated morphology Dyskeratosis false Inferred relationship Some 2
Autosomal dominant dyskeratosis congenita Finding site Skin structure false Inferred relationship Some 2
Autosomal dominant dyskeratosis congenita Associated morphology Developmental abnormality false Inferred relationship Some 3
Autosomal dominant dyskeratosis congenita Occurrence Congenital false Inferred relationship Some 3
Autosomal dominant dyskeratosis congenita Finding site Skin structure false Inferred relationship Some 3
Autosomal dominant dyskeratosis congenita Occurrence Congenital true Inferred relationship Some 1
Autosomal dominant dyskeratosis congenita Associated morphology Dyskeratosis true Inferred relationship Some 1
Autosomal dominant dyskeratosis congenita Finding site Skin structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Revesz syndrome Is a True Autosomal dominant dyskeratosis congenita Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start