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10866001: congenitale pancreasenterokinasedeficiëntie (aandoening)


    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
    18870014 Congenital pancreatic enterokinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
    603257011 Congenital pancreatic enterokinase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
    5924601000146119 congenitale pancreasenterokinasedeficiëntie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    5924611000146117 congenitale pancreasenterokinasedeficiëntie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
    6103161000146115 congenitale deficiëntie van pancreasenterokinase nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


    0 descendants.

    Expanded Value Set


    Outbound Relationships Type Target Active Characteristic Refinability Group Values
    congenitale pancreasenterokinasedeficiëntie Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Malabsorption syndrome false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Congenital malformation of pancreas false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Enzymopathy false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Autosomal recessive hereditary disorder false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Associated morphology Congenital deficiency false Inferred relationship Some 1
    congenitale pancreasenterokinasedeficiëntie Finding site Structure of small intestine (body structure) false Inferred relationship Some 2
    congenitale pancreasenterokinasedeficiëntie Occurrence Congenital false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Finding site Pancreatic structure false Inferred relationship Some 1
    congenitale pancreasenterokinasedeficiëntie Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 2
    congenitale pancreasenterokinasedeficiëntie Finding site Digestive organ structure false Inferred relationship Some 2
    congenitale pancreasenterokinasedeficiëntie Is a Disorder of small intestine false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a enterokinasedeficiëntie false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Congenital anomaly of trunk false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Occurrence Congenital false Inferred relationship Some 1
    congenitale pancreasenterokinasedeficiëntie Is a Congenital anomaly of pancreas false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Congenital anomaly of body cavity false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Congenital anomaly of abdomen false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Abdominal organ finding false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Associated morphology Congenital deficiency false Inferred relationship Some 1
    congenitale pancreasenterokinasedeficiëntie Finding site Pancreatic structure false Inferred relationship Some 2
    congenitale pancreasenterokinasedeficiëntie Is a Disorder of pancreas false Inferred relationship Some
    congenitale pancreasenterokinasedeficiëntie Is a Hereditary disorder of endocrine system (disorder) false Inferred relationship Some

    Inbound Relationships Type Active Source Characteristic Refinability Group

    Reference Sets

    Concept inactivation indicator reference set

    REPLACED BY association reference set (foundation metadata concept)

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