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205483007: Hypochondrogenesis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypochondrogenesis	Is a	Spondyloepiphyseal dysplasia congenita group (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypochondrogenesis	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypochondrogenesis	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypochondrogenesis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypochondrogenesis	Finding site	Skeletal system structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypochondrogenesis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypochondrogenesis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypochondrogenesis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypochondrogenesis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hypochondrogenesis	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hypochondrogenesis	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hypochondrogenesis	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hypochondrogenesis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
315102015	Hypochondrogenesis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
590856010	Hypochondrogenesis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
315102015	Hypochondrogenesis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
315102015	Hypochondrogenesis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
590856010	Hypochondrogenesis (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
590856010	Hypochondrogenesis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3412141001000114	Hypochondrogenesie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
983061000172111	hypochondrogenèse	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
983061000172111	hypochondrogenèse	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3412141001000114	Hypochondrogenesie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module