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770567006: Progeroid syndrome Petty type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3701302010 Progeroid syndrome Petty type en Synonym Active Only initial character case insensitive SNOMED CT core module
3701303017 Progeroid syndrome Petty type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3701304011 Petty syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3701307016 Petty Laxova Wiedemann syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Progeroid syndrome Petty type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Progeroid syndrome Petty type Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Progeroid syndrome Petty type Is a Premature aging syndrome true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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