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

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
172109016 Cellular AND/OR subcellular abnormality en Synonym Active Only initial character case insensitive SNOMED CT core module
593432018 Cellular AND/OR subcellular abnormality (morphologic abnormality) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

387 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 true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Koolen De Vries syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 3
Aggregated spermatozoa Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier
Myeloid leukemia co-occurrent with Down syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 5
Clue cell Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier
Oval fat body Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier
Agglutinated spermatozoa Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier
48,XYYY syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 1
Koolen De Vries syndrome Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 1
Congenital hereditary endothelial dystrophy and perceptive deafness syndrome Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 1
[X]Other male with 46,XX karyotype Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 2
[X]Other specified sex chromosome abnormalities, male phenotype Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 2
[X]Sex chromosome abnormality, male phenotype, unspecified Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 2
[X]Other deletions of part of a chromosome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 2
[X]Other deletions from the autosomes Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 2
[X]Other specified sex chromosome abnormalities, female phenotype Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier 2

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