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11599001: Hereditary disease in family possibly affecting fetus (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
20049016 Hereditary disease in family possibly affecting fetus en Synonym Active Entire term case insensitive SNOMED CT core module
673895015 Hereditary disease in family possibly affecting fetus (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3010444012 Hereditary disease in family possibly affecting foetus 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
Hereditary disease in family possibly affecting fetus Is a Hereditary disease 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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