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205838004: Congenital hemihypertrophy (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
315645014 Congenital hemihypertrophy en Synonym Active Entire term case insensitive SNOMED CT core module
2731067011 Congenital hemihypertrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hemihypertrophy Is a Congenital malformation true Inferred relationship Existential restriction modifier
Congenital hemihypertrophy Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital hemihypertrophy Associated morphology Congenital hemihypertrophy false Inferred relationship Existential restriction modifier 1
Congenital hemihypertrophy Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital hemihypertrophy Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 1
Congenital hemihypertrophy Is a Finding of body region false Inferred relationship Existential restriction modifier
Congenital hemihypertrophy Is a Disorder by body site false Inferred relationship Existential restriction modifier
Congenital hemihypertrophy Finding site Structure of half of body lateral to midsagittal plane 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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