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725904009: Genochondromatosis 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
3446272018 Genochondromatosis type 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3446273011 Genochondromatosis type 2 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
Genochondromatosis type 2 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Genochondromatosis type 2 Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier
Genochondromatosis type 2 Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Genochondromatosis type 2 Is a Genochondromatosis true Inferred relationship Existential restriction modifier
Genochondromatosis type 2 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Genochondromatosis type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Genochondromatosis type 2 Finding site Bone structure false Inferred relationship Existential restriction modifier 2
Genochondromatosis type 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Genochondromatosis type 2 Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Genochondromatosis type 2 Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Genochondromatosis type 2 Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Genochondromatosis type 2 Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Genochondromatosis type 2 Finding site Cartilage structure true Inferred relationship Existential restriction modifier 2
Genochondromatosis type 2 Is a Osteochondropathy true Inferred relationship Existential restriction modifier
Genochondromatosis type 2 Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Genochondromatosis type 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Genochondromatosis type 2 Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Genochondromatosis type 2 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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