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NCIm Version: 201706 (Browser Version 2.9, using LexEVS 6.5.1)
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XYY Karyotype (CUI C0043379) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0043379

Semantic Type: Disease or Syndrome

Semantic Type: Congenital Abnormality

MSH Definition: Abnormal genetic constitution in males characterized by an extra Y chromosome.

Synonyms & Abbreviations: (see Synonym Details)
Karyotype 47, XYY
Karyotype 47,XYY
Karyotype, XYY
Karyotypes, XYY
XYY Karyotypes
XYY Karyotype

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
AN do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; check the tags HUMANS & MALE MSH
AQL BL CF CI CL DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT UR VE VI MSH
DC 1 MSH
DX 19910101 MSH
HN 91(78); was see under SEX CHROMOSOME ABNORMALITIES 1978-90 MSH
IAN DEFAULT ICD10
MDA 19770422 MSH
MMR 20130708 MSH
MN C23.550.210.024.500 MSH
MN C23.550.210.815.970 MSH
MN G05.360.162.679.500.500 MSH
MN G05.365.590.175.024.500 MSH
MN G05.365.590.175.815.970 MSH
ORDER_NO 28213 ICD10CM
PM 91; was see under SEX CHROMOSOME ABNORMALITIES 1978-90 MSH
TERMUI T043777 MSH
TH BIOETHICS (1975) MSH
TH GHR (2014) MSH
TH ORD (2010) MSH

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0043379

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