205624009: Trisomy 18 - mitotic nondisjunction mosaicism (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Whole chromosome trisomy - mitotic nondisjunction mosaicism\Trisomy 18 - mitotic nondisjunction mosaicism
\Chromosomal disorder\Autosomal chromosomal disorder\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism
\Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Whole chromosome trisomy - mitotic nondisjunction mosaicism\Trisomy 18 - mitotic nondisjunction mosaicism
\Chromosomal disorder\Duplication of chromosome\Autosomal duplication\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism
\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 18\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism
\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Whole chromosome trisomy - mitotic nondisjunction mosaicism\Trisomy 18 - mitotic nondisjunction mosaicism
\Chromosomal disorder\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism

\Congenital disease\Congenital malformation\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Anomaly of chromosome pair\Anomaly of chromosome pair 18\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Whole chromosome trisomy - mitotic nondisjunction mosaicism\Trisomy 18 - mitotic nondisjunction mosaicism
\Congenital disease\Congenital disorder due to abnormality of chromosome number OR structure\Trisomy and partial trisomy of autosome\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism

\Developmental disorder\Congenital malformation\Complete trisomy 18 syndrome\Trisomy 18 - mitotic nondisjunction mosaicism

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

315355019 Trisomy 18 - mitotic nondisjunction mosaicism en Synonym Active Entire term case insensitive SNOMED CT core module

591019010 Trisomy 18 - mitotic nondisjunction mosaicism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Trisomy 18 - mitotic nondisjunction mosaicism	Is a	Complete trisomy 18 syndrome	true	Inferred relationship	Existential restriction modifier
Trisomy 18 - mitotic nondisjunction mosaicism	Associated morphology	Alteration of chromosome structure	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Sex chromosome	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - mitotic nondisjunction mosaicism	Associated morphology	Trisomy	true	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	true	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Associated morphology	Trisomy	false	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Trisomy 18 - mitotic nondisjunction mosaicism	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Associated morphology	Cellular AND/OR subcellular abnormality	false	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Finding site	Chromosome pair 18	true	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Is a	Whole chromosome trisomy - mitotic nondisjunction mosaicism	true	Inferred relationship	Existential restriction modifier
Trisomy 18 - mitotic nondisjunction mosaicism	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Trisomy 18 - mitotic nondisjunction mosaicism	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Associated morphology	Chromosome mosaicism	true	Inferred relationship	Existential restriction modifier	2
Trisomy 18 - mitotic nondisjunction mosaicism	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
315355019	Trisomy 18 - mitotic nondisjunction mosaicism	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
591019010	Trisomy 18 - mitotic nondisjunction mosaicism (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module