FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1197417009: Congenital portosystemic shunt (disorder)


    Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2022. Module: SNOMED CT core

    Descriptions:

    Id Description Lang Type Status Case? Module
    4696266018 A rare congenital anomaly of the great veins characterised by an abnormal communication between one or more veins of the portal and the caval systems, resulting in complete or partial diversion of the portal blood away from the liver to the systemic circulation. Clinical manifestations include liver atrophy, hypergalactosaemia without uridine diphosphate enzyme deficiency, hyperammonaemia, encephalopathy (resulting in learning disabilities, extreme fatigability and seizures), pulmonary hypertension, hypoxaemia from hepatopulmonary syndrome and benign or malignant tumours. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    4696267010 A rare congenital anomaly of the great veins characterized by an abnormal communication between one or more veins of the portal and the caval systems, resulting in complete or partial diversion of the portal blood away from the liver to the systemic circulation. Clinical manifestations include liver atrophy, hypergalactosemia without uridine diphosphate enzyme deficiency, hyperammonemia, encephalopathy (resulting in learning disabilities, extreme fatigability and seizures), pulmonary hypertension, hypoxemia from hepatopulmonary syndrome and benign or malignant tumors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
    4696263014 Congenital portosystemic shunt (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4696264015 Congenital portosystemic venous fistula en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    4696265019 Congenital portosystemic shunt en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    3427071001000112 Portosystemischer Shunt, kongenitaler de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    Portosystemischer Shunt, kongenitaler Is a Disorder of portal venous system false Inferred relationship Some
    Portosystemischer Shunt, kongenitaler Is a Anomalies of great veins false Inferred relationship Some
    Portosystemischer Shunt, kongenitaler Is a Congenital abnormality of vein false Inferred relationship Some
    Portosystemischer Shunt, kongenitaler Is a Congenital anomaly of abdomen false Inferred relationship Some
    Portosystemischer Shunt, kongenitaler Is a Congenital anomaly of cardiovascular structure of trunk false Inferred relationship Some
    Portosystemischer Shunt, kongenitaler Occurrence Congenital false Inferred relationship Some 1
    Portosystemischer Shunt, kongenitaler Finding site Structure of great vein (body structure) false Inferred relationship Some 1
    Portosystemischer Shunt, kongenitaler Associated morphology Abnormal communication false Inferred relationship Some 1
    Portosystemischer Shunt, kongenitaler Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
    Portosystemischer Shunt, kongenitaler Occurrence Congenital false Inferred relationship Some 2
    Portosystemischer Shunt, kongenitaler Finding site Portal venous system structure false Inferred relationship Some 2
    Portosystemischer Shunt, kongenitaler Associated morphology Abnormal communication false Inferred relationship Some 2
    Portosystemischer Shunt, kongenitaler Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    GB English

    US English

    SAME AS association reference set (foundation metadata concept)

    Back to Start