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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
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

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 true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Toxic leukocyte granulations (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Leukocytic agglutination Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Chromosomal morphology (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cellular hormonal pattern Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cellular stain reaction Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Dual red blood cell population Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Abnormal cell structure (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Rosette (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cell shape alteration Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Axonal swelling Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cell size alteration Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cell content alteration Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Clasmatodendrosis Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cytologic engulfment (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Nuclear lead inclusion (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Nuclear size alteration Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cytoplasmic aggregate Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cytoplasmic accumulation Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cytoplasmic droplets Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Myelin body formation Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Alteration of mitochondrial cristae (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Fungal cytoplasmic inclusion body Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Plasma membrane globulin coating Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Intracytoplasmic microvilli (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Flagella alteration Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Extracellular alteration (morphologic abnormality) Is a False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Basement membrane-like material (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Reticulin fibril alteration Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Collagen fibril alteration Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Extracellular granule alteration Is a False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Extracellular vacuole alteration Is a False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Extracellular space alteration Is a False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Extracellular fluid alteration Is a False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Reactive cellular changes Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Hyperparakeratosis (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Herring's bodies Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Russell body Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Muscle fiber change Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Leukostasis (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Flexner-Wintersteiner rosette Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Rouleaux formation Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Homer Wright rosette Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Heinz body (morphologic abnormality) Is a False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Cytologic atypia Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Satellitosis (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Leukocytic margination Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Margination Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Charcot-Leyden crystals Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
May-Hegglin inclusion Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Neuronophagia Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Mosaicism Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Epithelial cell abnormality (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Erythrocyte inclusion (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Fleurette (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Transitional cell dysplasia (morphologic abnormality) Is a True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept)
Complete trisomy 9 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Ring chromosome 10 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Trisomy X syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Sex chromosome abnormality - male phenotype Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Partial trisomy 13 in Patau's syndrome (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 21 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome Y Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, mosaicism 45, X; 46, XX or 45, X; 46, XY Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Female with more than three X chromosomes (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 13 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hereditary endothelial dystrophy Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 2
Anomaly of chromosome pair Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 22 syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 15 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Karyotype 46, X with abnormal sex chromosome except iso (Xq) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 2 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Mosaic XO/XY Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Mosaic including XXXXY Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Partial tetrasomy of chromosome 9 (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Sex chromosome abnormality - female phenotype Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Cat eye syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 14 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Turner's phenotype, karyotype normal (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Gynandromorphism syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 17 (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 10 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Translocation Down syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 14 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
An autosomal anomaly with characteristics of variable clinical features, most commonly including growth retardation, developmental delay, intellectual disability, epilepsy, microcephaly, short stature, dysmorphic features, hypogammaglobulinaemia, thrombocytopenia and unspecific skeletal anomalies (hemivertebrae, clinodactyly, syndactyly). In rare cases, it has been described in phenotypically normal individuals. Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Complete trisomy 18 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 5 (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Poly Y syndrome Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 6 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Ring chromosome 11 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Partial trisomy 18 in Edward's syndrome (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
XXXXY syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
XX males Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 10 (disorder) Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Disease marked by a characteristic seizure phenotype. Depending on the amount of chromosomal loss and associated mosaicism, ring(20) can be associated with macrocephaly, mild to moderate intellectual deficit, or behavioral problems. In rare cases, brain, kidney or heart malformations may be present. Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 20 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Ring chromosome 4 syndrome Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 21 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Anomaly of chromosome pair 8 Associated morphology True Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Chromosome 16p11.2 deletion syndrome (disorder) Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 1
Polymorphous corneal dystrophy Associated morphology False Cellular AND/OR subcellular abnormality Inferred relationship Existential restriction modifier (core metadata concept) 2

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