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239084001: Naegeli-Franceschetti-Jadassohn syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
358296016 Naegeli-Franceschetti-Jadassohn syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
358297013 Naegeli's syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
358298015 Franceschetti-Jadassohn syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
628052018 Naegeli-Franceschetti-Jadassohn syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Naegeli-Franceschetti-Jadassohn syndrome Is a Inherited cutaneous hyperpigmentation true Inferred relationship Existential restriction modifier
Naegeli-Franceschetti-Jadassohn syndrome Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 2
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Naegeli-Franceschetti-Jadassohn syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Naegeli-Franceschetti-Jadassohn syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Naegeli-Franceschetti-Jadassohn syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Naegeli-Franceschetti-Jadassohn syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Naegeli-Franceschetti-Jadassohn syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Naegeli-Franceschetti-Jadassohn syndrome Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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