Nondisjunction

Preferred Label : Nondisjunction;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Mosaicism, chromosomal; Mixoploidy, familial;

Description : Chromosomal mosaicism as described here refers to a tendency to chromosomal nondisjunction. See also premature chromatid separation (PCS; 165430), which may also predispose to chromosomal nondisjunction.;

Inheritance : Autosomal dominant; Autosomal recessive;

Laboratory abnormalities : Chromosomal mosaicism in cultured cells;

Prefixed ID : 158250;

Details

Origin ID

158250;

UMLS CUI

C1834741;

Automatic exact mappings (from CISMeF team)
- Chromosome mosaicism (morphologic abnormality) [SNOMED CT concept]
- chromosome mosaicism [SNOMED Notion]
- nondisjunction, genetic [MeSH Descriptor]
HPO term(s)
- Abnormality of chromosome segregation [HPO term]
- Autosomal dominant inheritance [HPO term]
- Autosomal recessive inheritance [HPO term]
- Decreased fertility [HPO term]
See also inter- (CISMeF)
- mosaic variegated aneuploidy syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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