107673000: Cellular AND/OR subcellular abnormality (morphologic abnormality)

SNOMED CT Concept\Body structure\Morphologically altered structure\Morphologically abnormal structure\Cellular AND/OR subcellular abnormality

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

Descriptions:

Id Description Lang Type Status Case? Module

172109016 Cellular AND/OR subcellular abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

593432018 Cellular AND/OR subcellular abnormality (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

172109016 Cellular AND/OR subcellular abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

593432018 Cellular AND/OR subcellular abnormality (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

65111000077114 anomalie cellulaire et/ou subcellulaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

65111000077114 anomalie cellulaire et/ou subcellulaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Cellular AND/OR subcellular abnormality	Is a	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Koolen De Vries syndrome (disorder)	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Aggregated spermatozoa (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)
Myeloid leukemia associated with Down syndrome (disorder)	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Clue cell	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)
Oval fat body (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)
Agglutinated spermatozoa (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)
48,XYYY syndrome (disorder)	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Koolen De Vries syndrome (disorder)	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Corneal dystrophy-perceptive deafness (CDPD) or Harboyan syndrome is a degenerative corneal disorder characterized by the association of congenital hereditary endothelial dystrophy with progressive, postlingual sensorineural hearing loss.	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Existential restriction modifier (core metadata concept)	1

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This concept is not in any reference sets