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

SNOMED CT Concept\Body structure\Body structure, altered from its original anatomical structure (morphologic abnormality)\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

2848181000005114 cellulært OG/ELLER subcellulær abnormitet da Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Danish module (core metadata concept)

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	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Toxic leukocyte granulations	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Leukocytic agglutination	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Chromosomal morphology	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cellular hormonal pattern	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cellular stain reaction	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Dual red blood cell population	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Abnormal cell structure	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Rosette	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cell shape alteration	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Axonal swelling (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cell size alteration	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cell content alteration	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Clasmatodendrosis	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cytologic engulfment	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Nuclear lead inclusion	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Nuclear size alteration	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cytoplasmic aggregate	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cytoplasmic accumulation	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cytoplasmic droplets	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Myelin body formation	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Alteration of mitochondrial cristae	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Fungal cytoplasmic inclusion body	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Plasma membrane globulin coating	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Intracytoplasmic microvilli	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Flagella alteration	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Extracellular alteration	Is a	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Basement membrane-like material (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Reticulin fibril alteration	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Collagen fibril alteration (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Extracellular granule alteration	Is a	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Extracellular vacuole alteration	Is a	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Extracellular space alteration	Is a	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Extracellular fluid alteration	Is a	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Reactive cellular changes	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Hyperparakeratosis	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Herring's bodies	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Russell body	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Muscle fiber change	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Leukostasis	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Flexner-Wintersteiner rosette	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Rouleaux formation (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Homer Wright rosette	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Heinz body	Is a	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Cytologic atypia	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Satellitosis	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Leukocytic margination	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Margination	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Charcot-Leyden crystals	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
May-Hegglin inclusion	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Neuronophagia	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Mosaicism	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Epithelial cell abnormality (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Erythrocyte inclusion (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Fleurette (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Transitional cell dysplasia (morphologic abnormality)	Is a	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some
Complete trisomy 9 syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
An autosomal anomaly with characteristics of variable clinical features, depending on the size and precise location of deleted chromosome segments. Most patients present with developmental delay, intellectual disability, growth retardation, microcephaly, clinodactyly and dysmorphic features. Congenital heart disease and genitourinary anomalies are reported in some cases.	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Trisomy X syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Sex chromosome abnormality - male phenotype	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Partial trisomy 13 in Patau's syndrome	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Complete trisomy 21 syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome Y	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Turners fænotype, mosaicisme 45, X; 46, XX eller 45, X; 46, XY	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Female with more than three X chromosomes	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 13	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Congenital hereditary endothelial dystrophy (disorder)	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	2
Anomaly of chromosome pair	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Complete trisomy 22 syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 15	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Turner syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Karyotype 46, X with abnormal sex chromosome except iso (Xq)	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 2	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Mosaic XO/XY	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Mosaic including XXXXY	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Partial tetrasomy of chromosome 9 (disorder)	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Sex chromosome abnormality - female phenotype	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
A rare chromosomal disorder with a highly variable clinical presentation. Most patients have multiple malformations affecting the eyes (iris coloboma), ears (preauricular pits and/or tags), anal region (anal atresia), heart and kidneys. Intellectual disability is usually mild or borderline normal. Most patients have a small supernumerary bi-satellited marker chromosome that results in partial tetrasomy of 22pter-22q11. In one third of cases, this extra chromosome is present in a mosaic state. Other cytogenetic anomalies have been rarely reported, including partial trisomy of chromosome 22 and intrachromosomal triplication of the 22q11 region.	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Komplet trisomi 14-syndrom	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Turner's phenotype, karyotype normal	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Gynandromorphism syndrome (disorder)	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 17	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Komplet trisomi 10-syndrom	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Translocation Down syndrome (disorder)	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 14	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	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	Some	1
Complete trisomy 18 syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 5	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Poly Y syndrome (disorder)	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 6	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
An autosomal anomaly with characteristics of variable clinical features, including early growth retardation and short stature, microcephaly, developmental delay, some degree of intellectual disability, facial dysmorphism and cafe-au-lait spots. In some cases, congenital heart disease and endocrine abnormalities have been reported.	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Partial trisomy 18 in Edward's syndrome	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
XXXXY syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
XX males	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 10	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	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	Some	1
Anomaly of chromosome pair 20	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
An autosomal anomaly with characteristics of variable clinical features, most commonly including significant intrauterine and postnatal growth retardation, developmental delay, intellectual disability, microcephaly, and dysmorphic facial features. Some less frequent features are cleft lip and/or cleft palate, congenital cardiovascular, gastrointestinal and genitourinary system anomalies.	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 21	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Anomaly of chromosome pair 8	Associated morphology	True	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Chromosome 16p11.2 deletion syndrome	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	1
Polymorphous corneal dystrophy	Associated morphology	False	Cellular AND/OR subcellular abnormality	Inferred relationship	Some	2

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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
2848181000005114	cellulært OG/ELLER subcellulær abnormitet	da	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Danish module (core metadata concept)