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708536001: X-linked dyskeratosis congenita (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3034737016 X-linked dyskeratosis congenita (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3034749015 X-linked dyskeratosis congenita en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3034737016 X-linked dyskeratosis congenita (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3034749015 X-linked dyskeratosis congenita en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked dyskeratosis congenita (disorder) Is a Dyskeratosis congenita true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked dyskeratosis congenita (disorder) Is a X-linked hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
X-linked dyskeratosis congenita (disorder) Associated morphology Dyskeratosis false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked dyskeratosis congenita (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked dyskeratosis congenita (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked dyskeratosis congenita (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked dyskeratosis congenita (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked dyskeratosis congenita (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked dyskeratosis congenita (disorder) Associated morphology Dyskeratosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked dyskeratosis congenita (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked dyskeratosis congenita (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked dyskeratosis congenita (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked dyskeratosis congenita (disorder) Finding site Ectoderm structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked dyskeratosis congenita (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked dyskeratosis congenita (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
A very rare X-linked recessive disorder considered to be a severe variant of dyskeratosis congenita, characterised by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anaemia. Is a True X-linked dyskeratosis congenita (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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