skip navigation links
National Cancer Institute
Enterprise Vocabulary Services
Box
NCIm Version: 201808 (Browser Version 2.9, using LexEVS 6.5.1)
SearchBox Top
SearchBox Bottom
Multiple congenital anomalies (CUI C0000772) Suggest changes to this concept
Add to Cart

Terms & Properties

Concept Unique Identifier (CUI): C0000772

Semantic Type: Congenital Abnormality

MSH Definition: Congenital abnormalities that affect more than one organ or body structure.

Synonyms & Abbreviations: (see Synonym Details)
ABNORM MULTIPLE
Abnormalities, Multiple [Disease/Finding]
Abnormalities, Multiple
ANOMALIES CONGENITAL MULTIPLE
ANOMALY CONGENITAL MULTIPLE (NOS)
Congenital anomaly, multiple NOS
Congenital deformity, multiple NOS
MALFORMATIONS MULTIPLE
Multiple Abnormalities
MULTIPLE ABNORM
Multiple cong anomalies
Multiple congenital abnormalities
Multiple congenital anomalies NOS
Multiple congenital anomalies, so described
MULTIPLE CONGENITAL ANOMALIES
Multiple congenital deformities NOS
Multiple congenital malformations

External Source Codes:  (none)

Other Properties: Property Definitions
Name Value Source
AN coordinate with specific abnormalities 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 SU TH UR VE VI MSH
DC 1 MSH
DX 19680101 MSH
FX D008607 MSH
HN 68 MSH
IPX -Q85 ICPC
IPX -Q86 ICPC
IPX -Q87 ICPC
IPX -Q89.R ICPC
IPX -Q90 ICPC
IPX -Q91 ICPC
IPX -Q92 ICPC
IPX -Q93 ICPC
IPX -Q95 ICPC
IPX -Q96 ICPC
IPX -Q97 ICPC
IPX -Q98 ICPC
IPX -Q99 ICPC
MDA 19990101 MSH
MESH_DUI D000015 NDFRT
MESH_NAME Abnormalities, Multiple NDFRT
MESH_UI M0000015 NDFRT
MMR 20151201 MSH
MN C16.131.077 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NUI N0000000266 NDFRT
PM 68 MSH
PRIMARY_PATH 10028182$10010445$10027664$10010331$Multiple congenital abnormalities$Congenital disorders NEC$Congenital and hereditary disorders NEC$Congenital, familial and genetic disorders MDR
PRIMARY_SOC 10010331 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 20.0 MDR
PT_IN_VERSION 20.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RXAUI 3104411 RXNORM
RXAUI 3104412 RXNORM
RXAUI 3200032 RXNORM
RXCUI 1023723 RXNORM
SMQ_TERM_ADDVERSION 10.0 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 14.0 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 116022009 NDFRT
TERMUI T000035 MSH
TERMUI T000036 MSH
TH NLM (1968) MSH
TH UNK (19XX) MSH

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0000772

Mainbox Bottom