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238061001: Neonatal adrenoleukodystrophy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356843012 Neonatal adrenoleucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035476014 Neonatal adrenoleukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4637152014 Neonatal adrenoleukodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
356843012 Neonatal adrenoleucodystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
356843012 Neonatal adrenoleucodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626892013 Neonatal adrenoleucodystrophy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
626892013 Neonatal adrenoleucodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3035476014 Neonatal adrenoleukodystrophy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3035476014 Neonatal adrenoleukodystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4637152014 Neonatal adrenoleukodystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3430711001000117 Adrenoleukodystrophie, neonatale Form de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
896151000172114 adrénoleucodystrophie néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
960521000172115 NALD - neonatal adrenoleukodystrophy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
896151000172114 adrénoleucodystrophie néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
960521000172115 NALD - neonatal adrenoleukodystrophy fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3430711001000117 Adrenoleukodystrophie, neonatale Form 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
Neonatal adrenoleucodystrophy Is a General loss of peroxisomal function (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Is a Adrenoleukodystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Finding site Adrenal cortex structure false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Occurrence Neonatal false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Is a Neonatal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal adrenoleucodystrophy Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal adrenoleucodystrophy Is a Peroxisome biogenesis disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal adrenoleucodystrophy Finding site Myelinated nerve fiber structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal adrenoleucodystrophy Associated morphology Myelin sheath alteration true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal adrenoleucodystrophy Finding site White matter structure of brain and spinal cord (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Neonatal adrenoleucodystrophy Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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