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725050005: Autosomal dominant osteopetrosis type 2 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3437498017 Autosomal dominant osteopetrosis type 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3437499013 Autosomal dominant osteopetrosis type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
3437500016 Albers Schonberg osteopetrosis en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant osteopetrosis type 2 Is a Osteopetrosis true Inferred relationship Existential restriction modifier
Autosomal dominant osteopetrosis type 2 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant osteopetrosis type 2 Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal dominant osteopetrosis type 2 Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Autosomal dominant osteopetrosis type 2 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Autosomal dominant osteopetrosis type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant osteopetrosis type 2 Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant osteopetrosis type 2 Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant osteopetrosis type 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant osteopetrosis type 2 Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Autosomal dominant osteopetrosis type 2 Interprets Osteoclast turnover rate true Inferred relationship Existential restriction modifier 2
Autosomal dominant osteopetrosis type 2 Clinical course Progressive 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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