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254055004: Atelosteogenesis type 2 (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
378199019 Atelosteogenesis type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
378200016 Atelosteogenesis de la Chapelle type en Synonym Active Only initial character case insensitive SNOMED CT core module
644894015 Atelosteogenesis type 2 (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
Atelosteogenesis type 2 Is a Atelosteogenesis true Inferred relationship Existential restriction modifier
Atelosteogenesis type 2 Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Occurrence Congenital false Inferred relationship Existential restriction modifier
Atelosteogenesis type 2 Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Atelosteogenesis type 2 Finding site Bone structure false Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 2 Associated morphology Dysplasia false Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 2 Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 2 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Atelosteogenesis type 2 Associated morphology Dislocation true Inferred relationship Existential restriction modifier 3
Atelosteogenesis type 2 Finding site Joint structure of multiple body sites true Inferred relationship Existential restriction modifier 3
Atelosteogenesis type 2 Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 2 Finding site Skeletal system structure false Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 2 Is a Disorder of bone development false Inferred relationship Existential restriction modifier
Atelosteogenesis type 2 Clinical course Progressive true Inferred relationship Existential restriction modifier 4
Atelosteogenesis type 2 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Atelosteogenesis type 2 Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Atelosteogenesis type 2 Due to Spontaneous event true Inferred relationship Existential restriction modifier 2
Atelosteogenesis type 2 Associated morphology Damage false Inferred relationship Existential restriction modifier 5
Atelosteogenesis type 2 Is a Bone injury 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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