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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


10200 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital disease (disorder) Is a Disease false Inferred relationship Some
Congenital disease (disorder) Occurrence Congenital true Inferred relationship Some 1
Congenital disease (disorder) Is a Disorder of foetus and/or newborn true Inferred relationship Some

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

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