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254061001: Achondrogenesis, type II (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
378208011 Achondrogenesis, type II en Synonym Active Only initial character case insensitive SNOMED CT core module
378209015 Langer-Saldino dysplasia en Synonym Active Entire term case sensitive SNOMED CT core module
378210013 Langer-Saldino achondrogenesis en Synonym Active Entire term case sensitive SNOMED CT core module
644901016 Achondrogenesis, type II (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Achondrogenesis, type II Is a Spondyloepiphyseal dysplasia congenita group true Inferred relationship Existential restriction modifier
Achondrogenesis, type II Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Occurrence Congenital false Inferred relationship Existential restriction modifier
Achondrogenesis, type II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Is a Achondrogenesis true Inferred relationship Existential restriction modifier
Achondrogenesis, type II Finding site Both lower extremities false Inferred relationship Existential restriction modifier
Achondrogenesis, type II Finding site Both upper extremities false Inferred relationship Existential restriction modifier
Achondrogenesis, type II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Achondrogenesis, type II Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Achondrogenesis, type II Finding site Bone structure true Inferred relationship Existential restriction modifier 2
Achondrogenesis, type II Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Achondrogenesis, type II Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Achondrogenesis, type II Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier 3
Achondrogenesis, type II Finding site Bone structure false Inferred relationship Existential restriction modifier 3
Achondrogenesis, type II Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Achondrogenesis, type II Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Achondrogenesis, type II Interprets Height / growth measure true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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