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1156768008: Ovarioleukodystrophy (disorder)


Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4576146013 Ovarioleukodystrophy en Synonym Active Case insensitive SNOMED CT core
4576147016 Ovarioleukodystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4577015016 Ovarioleucodystrophy en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ovarioleucodystrophy Associated morphology Myelin sheath alteration true Inferred relationship Some 1
Ovarioleucodystrophy Is a Vanishing white matter disease true Inferred relationship Some
Ovarioleucodystrophy Interprets Hormone secretion true Inferred relationship Some 3
Ovarioleucodystrophy Has interpretation Decreased true Inferred relationship Some 3
Ovarioleucodystrophy Finding site Cerebral white matter structure true Inferred relationship Some 2
Ovarioleucodystrophy Finding site Ovarian endocrine structure true Inferred relationship Some 4
Ovarioleucodystrophy Is a Hereditary disorder of endocrine system true Inferred relationship Some
Ovarioleucodystrophy Is a Reproductive system hereditary disorder true Inferred relationship Some
Ovarioleucodystrophy Finding site Myelinated nerve fibre structure true Inferred relationship Some 1
Ovarioleucodystrophy Associated morphology Dystrophy true Inferred relationship Some 2
Ovarioleucodystrophy Is a Premature ovarian failure true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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