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698601005: Single congenital anomaly (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2974838019 Single congenital anomaly en Synonym Active Entire term case insensitive SNOMED CT core module
2974959010 Single congenital anomaly (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3006500014 Single congenital malformation 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
Single congenital anomaly Is a Congenital anomaly false Inferred relationship Existential restriction modifier
Single congenital anomaly Occurrence Congenital false Inferred relationship Existential restriction modifier
Single congenital anomaly Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Single congenital anomaly Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Single congenital anomaly Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Single congenital anomaly Is a Congenital malformation true Inferred relationship Existential restriction modifier
Single congenital anomaly Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Single congenital anomaly Pathological process Pathological developmental process 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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