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720416007: Acrocapitofemoral dysplasia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3320688014 Acrocapitofemoral dysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3320689018 Acrocapitofemoral dysplasia 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
Acrocapitofemoral dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Acrocapitofemoral dysplasia Is a Acromesomelic dysplasia group true Inferred relationship Existential restriction modifier
Acrocapitofemoral dysplasia Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Acrocapitofemoral dysplasia Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Acrocapitofemoral dysplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Acrocapitofemoral dysplasia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Acrocapitofemoral dysplasia Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Acrocapitofemoral dysplasia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Acrocapitofemoral dysplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Acrocapitofemoral dysplasia Is a Developmental hereditary disorder 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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