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238061001: Neonatal adrenoleukodystrophy (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3035476014 Neonatal adrenoleukodystrophy en Synonym Active Case insensitive SNOMED CT core
356843012 Neonatal adrenoleucodystrophy en Synonym Active Case insensitive SNOMED CT core
4637152014 Neonatal adrenoleukodystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal adrenoleucodystrophy Occurrence Neonatal false Inferred relationship Some
Neonatal adrenoleucodystrophy Is a Neonatal disorder false Inferred relationship Some
Neonatal adrenoleucodystrophy Occurrence Congenital false Inferred relationship Some
Neonatal adrenoleucodystrophy Finding site Entire endocrine gonad false Inferred relationship Some
Neonatal adrenoleucodystrophy Finding site Adrenal cortex structure false Inferred relationship Some
Neonatal adrenoleucodystrophy Is a General loss of peroxisomal function false Inferred relationship Some
Neonatal adrenoleucodystrophy Is a Adrenoleucodystrophy true Inferred relationship Some
Neonatal adrenoleucodystrophy Occurrence Congenital true Inferred relationship Some 1
Neonatal adrenoleucodystrophy Finding site Adrenal cortex structure true Inferred relationship Some 1
Neonatal adrenoleucodystrophy Is a Peroxisome biogenesis disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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