268274005: Enchondromatosis (disorder)

SNOMED CT Concept\Clinical finding\...

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

400926013 Multiple enchondromata en Synonym Active Entire term case insensitive SNOMED CT core module
400927016 Congenital enchondromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
400928014 Ollier disease en Synonym Active Entire term case sensitive SNOMED CT core module
400929018 Dyschondroplasia en Synonym Active Entire term case insensitive SNOMED CT core module
400930011 Ollier's disease en Synonym Active Entire term case sensitive SNOMED CT core module
400931010 Enchondromatosis en Synonym Active Entire term case insensitive SNOMED CT core module
660995016 Enchondromatosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Maffucci syndrome	Is a	True	Enchondromatosis	Inferred relationship	Existential restriction modifier
Bone dysplasia Azouz type	Is a	False	Enchondromatosis	Inferred relationship	Existential restriction modifier
Dysspondyloenchondromatosis	Is a	True	Enchondromatosis	Inferred relationship	Existential restriction modifier
Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria	Is a	True	Enchondromatosis	Inferred relationship	Existential restriction modifier
Cheirospondyloenchondromatosis	Is a	True	Enchondromatosis	Inferred relationship	Existential restriction modifier
Metachondromatosis	Is a	True	Enchondromatosis	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets