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66091009: Congenital disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
109766011 Congenital disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500309015 Congenital abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
500310013 Fetal developmental abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011638011 Foetal developmental abnormality en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3921000077116 maladie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
10211000188115 pathologie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3921000077116 maladie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
10211000188115 pathologie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

10200 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital disease Is a Disease false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital disease Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital disease Is a Disorder of foetus and/or newborn true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
X-linked corneal dermoid (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
X-linked neurodegenerative syndrome Bertini type (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Isolated generalized anhidrosis with normal sweat glands (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Non-syndromic mitochondrial sensorineural deafness (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Nemaline myopathy, early onset type Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital palsy of trochlear nerve (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital oculomotor nerve palsy (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital horizontal gaze palsy (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Isolated congenital horizontal gaze paresis Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital monocular elevator palsy (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital isolated adrenocorticotropic hormone deficiency (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pseudopapilledema (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital insensitivity to pain with severe intellectual disability (disorder) Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital axonal neuropathy with encephalopathy Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital Horner syndrome Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of lysosomal enzyme Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cutaneous mastocytosis Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Cutis tricolor Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Congenital benign giant pigmented nevus of skin Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)
Mongolian spot Is a True Congenital disease Inferred relationship Existential restriction modifier (core metadata concept)

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