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708536001: X-linked dyskeratosis congenita (disorder)


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

Descriptions:

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


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked dyskeratosis congenita Is a Dyskeratosis congenita true Inferred relationship Existential restriction modifier
X-linked dyskeratosis congenita Is a X-linked hereditary disease true Inferred relationship Existential restriction modifier
X-linked dyskeratosis congenita Associated morphology Dyskeratosis false Inferred relationship Existential restriction modifier 2
X-linked dyskeratosis congenita Finding site Skin structure false Inferred relationship Existential restriction modifier 2
X-linked dyskeratosis congenita Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
X-linked dyskeratosis congenita Occurrence Congenital false Inferred relationship Existential restriction modifier 3
X-linked dyskeratosis congenita Finding site Skin structure false Inferred relationship Existential restriction modifier 3
X-linked dyskeratosis congenita Occurrence Congenital true Inferred relationship Existential restriction modifier 1
X-linked dyskeratosis congenita Associated morphology Dyskeratosis true Inferred relationship Existential restriction modifier 1
X-linked dyskeratosis congenita Finding site Skin structure true Inferred relationship Existential restriction modifier 1
X-linked dyskeratosis congenita Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
X-linked dyskeratosis congenita Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
X-linked dyskeratosis congenita Finding site Ectoderm structure true Inferred relationship Existential restriction modifier 2
X-linked dyskeratosis congenita Occurrence Congenital true Inferred relationship Existential restriction modifier 2
X-linked dyskeratosis congenita Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Hoyeraal-Hreidarsson syndrome Is a True X-linked dyskeratosis congenita Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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