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Congenital atresia of pulmonary valve (CUI C0242855) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0242855

NCI Thesaurus Code: C99031  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

Semantic Type: Congenital Abnormality

NCIt Definition: A congenital heart defect characterized by complete atresia of the pulmonary valve. It is manifested during infancy with cyanosis, dyspnea, and tachypnea.

HPO Definition: A congenital disorder of the pulmonary valve in which the orifice of the valve fails to develop. [HPO:probinson]

MSH Definition: A congenital heart defect characterized by the narrowing or complete absence of the opening between the RIGHT VENTRICLE and the PULMONARY ARTERY. Lacking a normal PULMONARY VALVE, unoxygenated blood in the right ventricle can not be effectively pumped into the lung for oxygenation. Clinical features include rapid breathing, CYANOSIS, right ventricle atrophy, and abnormal heart sounds (HEART MURMURS).

Synonyms & Abbreviations: (see Synonym Details)
Atresia of pulmonary valve (disorder)
Atresia of pulmonary valve, congenital
Atresia of pulmonary valve
ATRESIA PULM VALVE
ATRESIA PULM
Atresia, Pulmonary Valve
Atresia, Pulmonary
ATRESIAS PULM VALVE
ATRESIAS PULM
Atresias, Pulmonary Valve
Atresias, Pulmonary
Cong pulmon valv atresia
Congenital atresia of pulmonary valve
Congenital atresia of the pulmonary valve (disorder)
Congenital Atresia of the Pulmonary Valve
Congenital pulmonary valve atresia
PULM ATRESIAS
PULM ATRESIA
PULM VALVE ATRESIAS
PULM VALVE ATRESIA
Pulmonary Atresia [Disease/Finding]
Pulmonary Atresias
Pulmonary Atresia
Pulmonary Valve Atresias
Pulmonary valve atresia
Valve Atresia, Pulmonary
Valve Atresias, Pulmonary

External Source Codes: 
NCI Thesaurus Code C99031 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN DF: PULM ATRESIA 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 900000000000448009 SNOMEDCT_US
CHARACTERISTIC_TYPE_ID 900000000000011006 SNOMEDCT_US
Contributing_Source NICHD NCI
CTV3ID P601. SNOMEDCT_US
CTV3ID XUu8Y SNOMEDCT_US
DATE_CREATED 2010-09-20T11:08:09Z HPO
DC 1 MSH
DEFINITION_STATUS_ID 900000000000073002 SNOMEDCT_US
DX 19950101 MSH
EFFECTIVE_TIME 20050131 SNOMEDCT_US
EFFECTIVE_TIME 20170131 SNOMEDCT_US
HN 95 MSH
IAN DEFAULT ICD10
ICE Congenital absence of pulmonary valve ICD9CM
MDA 19940523 MSH
MESH_DEFINITION A congenital heart defect characterized by the narrowing or complete absence of the opening between the RIGHT VENTRICLE and the PULMONARY ARTERY. Lacking a normal PULMONARY VALVE, unoxygenated blood in the right ventricle can not be effectively pumped into the lung for oxygenation. Clinical features include rapid breathing, CYANOSIS, right ventricle atrophy, and abnormal heart sounds (HEART MURMURS). NDFRT
MESH_DUI D018633 NDFRT
MESH_NAME Pulmonary Atresia NDFRT
MESH_UI M0027926 NDFRT
MMR 20070709 MSH
MN C14.240.850.937 MSH
MN C14.280.484.640 MSH
MN C16.131.240.850.906 MSH
MODIFIER_ID 900000000000451002 SNOMEDCT_US
NDFRT_KIND DISEASE_KIND NDFRT
NICHD_Hierarchy_Term Pulmonary Valve Atresia NCI
NUI N0000003840 NDFRT
ORDER_NO 27402 ICD10CM
PM 95 MSH
PRIMARY_PATH 10052644$10007614$10007510$10010331$Congenital pulmonary valve atresia$Cardiac valve disorders congenital$Cardiac and vascular disorders congenital$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 3112253 RXNORM
RXAUI 3112254 RXNORM
RXAUI 3112260 RXNORM
RXAUI 3112261 RXNORM
RXAUI 3226009 RXNORM
RXAUI 3226010 RXNORM
RXAUI 3226011 RXNORM
RXAUI 3226119 RXNORM
RXAUI 3226120 RXNORM
RXCUI 1025941 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 204342004 NDFRT
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS Q22.0 | MAPPED FOLLOWING WHO GUIDANCE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS Q22.0 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~Q22.0 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS Q22.0 | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS Q22.0 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~Q22.0 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~P601. SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUu8Y 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 T055488 MSH
TERMUI T055489 MSH
TERMUI T055490 MSH
TERMUI T055491 MSH
TERMUI T055492 MSH
TERMUI T055493 MSH
TERMUI T055494 MSH
TERMUI T055495 MSH
TH NLM (1995) 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=C0242855

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