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41010001: Maturation defect (morphologic abnormality)


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
68413014 Maturation defect en Synonym Active Entire term case insensitive SNOMED CT core module
777750015 Maturation defect (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module


12 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Maturation defect Is a Growth alteration true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Impaired mineralization Is a True Maturation defect Inferred relationship Existential restriction modifier
Aplasia Is a True Maturation defect Inferred relationship Existential restriction modifier
Maturation deceleration Is a True Maturation defect Inferred relationship Existential restriction modifier
Hamartoma Is a False Maturation defect Inferred relationship Existential restriction modifier
Hypoplasia Is a True Maturation defect Inferred relationship Existential restriction modifier
Maturation acceleration Is a True Maturation defect Inferred relationship Existential restriction modifier
Atavism Is a True Maturation defect Inferred relationship Existential restriction modifier
Dedifferentiation Is a True Maturation defect Inferred relationship Existential restriction modifier
Cleidocranial dysostosis Associated morphology False Maturation defect Inferred relationship Existential restriction modifier 1
Cleidocranial dysostosis Associated morphology False Maturation defect Inferred relationship Existential restriction modifier 9
Cleidocranial dysostosis Associated morphology True Maturation defect Inferred relationship Existential restriction modifier 3
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Associated morphology True Maturation defect Inferred relationship Existential restriction modifier 1
Congenital deficiency of cochlear nerve Associated morphology True Maturation defect Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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