skip navigation links
National Cancer Institute
Enterprise Vocabulary Services
Box
NCIm Version: 201706 (Browser Version 2.9, using LexEVS 6.5.1)
SearchBox Top
SearchBox Bottom
Congenital neurologic anomalies (CUI C0497552) Suggest changes to this concept
Add to Cart

Terms & Properties

Concept Unique Identifier (CUI): C0497552

NCI Thesaurus Code: C97172  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

Semantic Type: Congenital Abnormality

NCIt Definition: An abnormality of the nervous system that is present at birth or detected in the neonatal period.

HPO Definition: An abnormality of the nervous system. [HPO:probinson]

CSP Definition: structural or functional abnormalities of the central or peripheral nervous system existing at birth and often before birth, resulting primarily from defects of embryogenesis.

MSH Definition: Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis.

Synonyms & Abbreviations: (see Synonym Details)
ABNORM CONGEN NERVOUS SYSTEM
ABNORM NERVOUS SYSTEM
Abnormalities, Congenital, Nervous System
Abnormalities, Nervous System
Abnormality of the nervous system
Abnormality, Nervous System
Anomalies, Nervous System
Anomaly, Nervous System
CONGEN ABNORM NERVOUS SYSTEM
CONGEN ANOMALIES NERVOUS SYSTEM
CONGEN MALFORMATIONS NERVOUS SYSTEM
Congenital Abnormalities, Nervous System
Congenital Abnormality of the Nervous System
Congenital Anomalies, Nervous System
Congenital anomaly NOS of nervous system
Congenital anomaly of nervous system (disorder)
Congenital anomaly of nervous system
Congenital deformity NOS of nervous system
Congenital deformity of nervous system
Congenital disease of nervous system
Congenital lesion of nervous system
Congenital malformation of nervous system, unspecified
Congenital malformation of the nervous system
Congenital malformations of the nervous system (Q00-Q07)
Congenital malformations of the nervous system
Congenital Malformations, Nervous System
congenital nervous system disorder
Congenital neurologic anomalies
Malformation, Nervous System
MALFORMATIONS NERVOUS SYSTEM CONGEN
Malformations, Nervous System, Congenital
Malformations, Nervous System
Nervous System Abnormalities
Nervous System Abnormality
NERVOUS SYSTEM ABNORM
Nervous system anom NOS
Nervous System Anomalies
Nervous System Anomaly
NERVOUS SYSTEM CONGEN ABNORM
NERVOUS SYSTEM CONGEN MALFORMATIONS
Nervous System Congenital Abnormalities
Nervous system congenital anomalies
Nervous System Congenital Malformations
Nervous System Malformations [Disease/Finding]
NERVOUS SYSTEM MALFORMATIONS CONGEN
Nervous System Malformations, Congenital
Nervous System Malformations
Nervous System Malformation
Neurologic abnormalities
Neurological abnormality
Unspecified congenital anomaly of brain, spinal cord, and nervous system

External Source Codes: 
NCI Thesaurus Code C97172 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN for congen struct abnorm only; GEN or unspecified; prefer specifics or specific organ/abnorm; DF: NERVOUS SYSTEM ABNORM MSH
AQL BL CF CI CL CO 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
CASE_SIGNIFICANCE_ID 900000000000020002 SNOMEDCT_US
Contributing_Source NICHD NCI
CTV3ID X00Ef SNOMEDCT_US
DC 1 MSH
DEFINITION_STATUS_ID 900000000000073002 SNOMEDCT_US
DID 0725-4145 CSP
DX 19980101 MSH
EFFECTIVE_TIME 20040731 SNOMEDCT_US
HN 2000(1966); use explode 1971-1997 MSH
HPO_COMMENT The nervous system comprises the neuraxis (brain, spinal cord, and ventricles), the autonomic nervous system, the enteric nervous system, and the peripheral nervous system. HPO
IAN DEFAULT ICD10
ICE Anomaly of brain, nervous system, and spinal cord; Congenital, of brain, nervous system, and spinal cord: {disease of brain, nervous system, and spinal cord; lesion of brain, nervous system, and spinal cord}; Deformity of brain, nervous system, and spinal cord ICD9CM
INCLUSION_TERM Congenital: anomaly NOS of nervous system ICD10
INCLUSION_TERM Congenital: deformity NOS of nervous system ICD10
INCLUSION_TERM Congenital: disease or lesion NOS of nervous system ICD10
MDA 19990101 MSH
MESH_DEFINITION Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis. NDFRT
MESH_DUI D009421 NDFRT
MESH_NAME Nervous System Malformations NDFRT
MESH_UI M0014666 NDFRT
MMR 20030709 MSH
MN C10.500 MSH
MN C16.131.666 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NICHD_Hierarchy_Term Congenital Nervous System Disorder NCI
NUI N0000002158 NDFRT
ORDER_NO 27310 ICD10CM
PM 2000; see NERVOUS SYSTEM ABNORMALITIES 1966-1999 MSH
RXAUI 3104397 RXNORM
RXAUI 3104414 RXNORM
RXAUI 3109463 RXNORM
RXAUI 3135287 RXNORM
RXAUI 3135296 RXNORM
RXAUI 3135357 RXNORM
RXAUI 3196314 RXNORM
RXAUI 3205779 RXNORM
RXAUI 3205784 RXNORM
RXAUI 3205791 RXNORM
RXAUI 3205792 RXNORM
RXAUI 3205824 RXNORM
RXAUI 3205825 RXNORM
RXAUI 3205826 RXNORM
RXCUI 1022724 RXNORM
SID HP:0001333 HPO
SID HP:0006987 HPO
SMQ_TERM_ADDVERSION 10.0 MDR
SMQ_TERM_CAT A 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 204093003 NDFRT
SNOMED_CID 88425004 NDFRT
SNOMEDID D4-90000 SNOMEDCT_US
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS Q07.9 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~Q07.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS Q07.9 | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~Q07.9 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~X00Ef SNOMEDCT_US
SUBSET_MEMBER 900000000000498005~MAPTARGET~D4-90000 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T028090 MSH
TERMUI T028091 MSH
TERMUI T365650 MSH
TERMUI T365652 MSH
TERMUI T365653 MSH
TERMUI T365654 MSH
TERMUI T365655 MSH
TERMUI T365656 MSH
TERMUI T365657 MSH
TERMUI T365658 MSH
TERMUI T365659 MSH
TERMUI T365660 MSH
TERMUI T373372 MSH
TH NLM (1966) MSH
TH NLM (1998) MSH
TH NLM (2000) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0497552

Mainbox Bottom