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107673000: Cellular AND/OR subcellular abnormality (morphologic 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

388 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cellular AND/OR subcellular abnormality Is a Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Koolen De Vries syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Some 3
Aggregated spermatozoa (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Some
Myeloid leukemia associated with Down syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Some 5
Clue cell (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Some
Oval fat body (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Some
Agglutinated spermatozoa (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Some
48,XYYY syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Some 1
Koolen De Vries syndrome (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Some 1
Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Some 1

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