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403275004: Alezzandrini syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1771201010 Alezzandrini syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1782330010 Alezzandrini syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Alezzandrini syndrome Is a Acquired hypomelanosis of uncertain etiology true Inferred relationship Existential restriction modifier
Alezzandrini syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Alezzandrini syndrome Associated morphology Structure showing abnormal deposition of pigment false Inferred relationship Existential restriction modifier 1
Alezzandrini syndrome Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier
Alezzandrini syndrome Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 1
Alezzandrini syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Alezzandrini syndrome Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 1
Alezzandrini syndrome Occurrence Period of life beginning after birth and ending before death 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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