105987004: Malformation defect spectrum (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

170406013 Malformation defect spectrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

576971014 Malformation defect spectrum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

170406013 Malformation defect spectrum en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

170406013 Malformation defect spectrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

576971014 Malformation defect spectrum (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

576971014 Malformation defect spectrum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Malformation defect spectrum	Is a	Multiple congenital malformations	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation defect spectrum	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation defect spectrum	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation defect spectrum	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Malformation defect spectrum	Is a	Congenital malformation syndrome	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Malformation defect spectrum	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Malformation defect spectrum	Associated morphology	Morphologically abnormal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Malformation defect spectrum	Pathological process (attribute)	Pathological developmental process (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Facio-auriculo-vertebral spectrum (disorder)	Is a	False	Malformation defect spectrum	Inferred relationship	Existential restriction modifier (core metadata concept)
A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies).	Is a	False	Malformation defect spectrum	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

POSSIBLY EQUIVALENT TO association reference set