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24216005: Congenital absence (morphologic abnormality)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
40644015 Congenital absence en Synonym Active Case insensitive SNOMED CT core
753828014 Congenital absence (morphologic abnormality) en Fully specified name Active Case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence Is a Aplasia true Inferred relationship Some
Congenital absence Is a Congenital anomaly false Inferred relationship Some
Congenital absence Is a Congenital malformation false Inferred relationship Some
Congenital absence Is a Absence false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Thumb deformity, alopecia, pigmentation anomaly syndrome Associated morphology False Congenital absence Inferred relationship Some 1
Ectodermal dysplasia syndactyly syndrome Associated morphology False Congenital absence Inferred relationship Some 3
Anencephalus and similar anomalies Associated morphology False Congenital absence Inferred relationship Some 1
Acrania Associated morphology False Congenital absence Inferred relationship Some 2
Cryptophthalmos syndrome Associated morphology False Congenital absence Inferred relationship Some 1
Agenesis of eyelid Associated morphology False Congenital absence Inferred relationship Some 1
Congenital absence of anus with fistula Associated morphology False Congenital absence Inferred relationship Some 1
Holt-Oram syndrome Associated morphology False Congenital absence Inferred relationship Some 1
Aglossia-adactyly syndrome Associated morphology False Congenital absence Inferred relationship Some 5

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Reference Sets

Body structure foundation reference set

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