FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.24 | FHIR Version n/a User: [n/a]

389264005: Genochondromatosis (disorder)

SNOMED CT Concept\Clinical finding\...

\Musculoskeletal finding\Cartilage finding\Cartilage disorder\Congenital anomaly of cartilage\Disorganized development of cartilaginous and fibrous components of the skeleton\Genochondromatosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Musculoskeletal and connective tissue disorder\Cartilage disorder\Congenital anomaly of cartilage\Disorganized development of cartilaginous and fibrous components of the skeleton\Genochondromatosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Congenital skeletal dysplasia\Disorganized development of cartilaginous and fibrous components of the skeleton\Genochondromatosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Cartilage disorder\Congenital anomaly of cartilage\Disorganized development of cartilaginous and fibrous components of the skeleton\Genochondromatosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital skeletal dysplasia\Disorganized development of cartilaginous and fibrous components of the skeleton\Genochondromatosis
\Musculoskeletal finding\Disorder of musculoskeletal system\Congenital anomaly of musculoskeletal system\Congenital anomaly of cartilage\Disorganized development of cartilaginous and fibrous components of the skeleton\Genochondromatosis

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2003. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

1463443015 Genochondromatosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1483301017 Genochondromatosis en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Genochondromatosis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Genochondromatosis	Is a	Disorganized development of cartilaginous and fibrous components of the skeleton	true	Inferred relationship	Existential restriction modifier
Genochondromatosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Genochondromatosis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Genochondromatosis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	1
Genochondromatosis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Genochondromatosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Genochondromatosis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier	2
Genochondromatosis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Genochondromatosis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Genochondromatosis	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Genochondromatosis	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Genochondromatosis	Finding site	Cartilage structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Genochondromatosis type 2	Is a	True	Genochondromatosis	Inferred relationship	Existential restriction modifier
Genochondromatosis type 1	Is a	True	Genochondromatosis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1463443015	Genochondromatosis (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
1483301017	Genochondromatosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module