FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.9.1  |  FHIR Version n/a  User: [n/a]

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
222001000000117 Franceschetti syndrome en Synonym Inactive Only initial character case insensitive SNOMED CT United Kingdom Edition 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

Back to Start