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1003918009: Pfeiffer syndrome type 3 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4166965011 Pfeiffer syndrome type 3 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4166966012 Pfeiffer syndrome type 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pfeiffer syndrome type 3 (disorder) est un(e) (attribut) acro-céphalo-syndactylie de type V true Inferred relationship Some
Pfeiffer syndrome type 3 (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Pfeiffer syndrome type 3 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Pfeiffer syndrome type 3 (disorder) morphologie associée (attribut) Congenital abnormal fusion true Inferred relationship Some 1
Pfeiffer syndrome type 3 (disorder) localisation d'une constatation (attribut) Digit structure true Inferred relationship Some 1
Pfeiffer syndrome type 3 (disorder) morphologie associée (attribut) Congenital premature fusion true Inferred relationship Some 2
Pfeiffer syndrome type 3 (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Pfeiffer syndrome type 3 (disorder) localisation d'une constatation (attribut) Joint structure of suture of skull true Inferred relationship Some 2
Pfeiffer syndrome type 3 (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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