65389002: Adrenoleukodystrophy (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Disorder of adrenal gland\...

\Hypoadrenalism\Adrenal insufficiency\Adrenoleucodystrophy

\Disorder of adrenal cortex\Adrenal insufficiency\Adrenoleucodystrophy

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Hypoadrenalism\Adrenal insufficiency\Adrenoleucodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal insufficiency\Adrenoleucodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Disorder of adrenal gland\Hypoadrenalism\Adrenal insufficiency\Adrenoleucodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal insufficiency\Adrenoleucodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Hypoadrenalism\Adrenal insufficiency\Adrenoleucodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal insufficiency\Adrenoleucodystrophy
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Hypoadrenalism\Adrenal insufficiency\Adrenoleucodystrophy
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal insufficiency\Adrenoleucodystrophy

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Adrenoleucodystrophy
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Adrenoleucodystrophy
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked dominant hereditary disease\Adrenoleucodystrophy
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Adrenoleucodystrophy
\Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Adrenoleucodystrophy
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of adrenal gland\Hypoadrenalism\Adrenal insufficiency\Adrenoleucodystrophy
\Disease\Disorder of body system\Disorder of endocrine system\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal insufficiency\Adrenoleucodystrophy
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Hypoadrenalism\Adrenal insufficiency\Adrenoleucodystrophy
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal insufficiency\Adrenoleucodystrophy
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Adrenoleucodystrophy
\Disease\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\Loss of single peroxisomal function\Adrenoleucodystrophy

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

Descriptions:

Id Description Lang Type Status Case? Module

108634018 Adrenoleukodystrophy en Synonym Active Case insensitive SNOMED CT core

108635017 Adrenomyeloneuropathy en Synonym Active Case insensitive SNOMED CT core

108637013 Bronze Schilder disease en Synonym Active Initial character case insensitive SNOMED CT core

108638015 Schilder-Addison complex en Synonym Active Case sensitive SNOMED CT core

108639011 Siemerling-Creutzfeldt disease en Synonym Active Case sensitive SNOMED CT core

1232670018 X-linked adrenoleucodystrophy en Synonym Active Case sensitive SNOMED CT core

2154288010 Adrenoleucodystrophy en Synonym Active Case insensitive SNOMED CT core

2957107010 ALD - adrenoleukodystrophy en Synonym Active Case sensitive SNOMED CT core

4637154010 X-linked adrenoleukodystrophy en Synonym Active Case sensitive SNOMED CT core

804886014 Adrenoleukodystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Adrenoleucodystrophy	Is a	X-linked dominant hereditary disease	true	Inferred relationship	Some
Adrenoleucodystrophy	Is a	Adrenal insufficiency	true	Inferred relationship	Some
Adrenoleucodystrophy	Is a	Loss of single peroxisomal function	true	Inferred relationship	Some
Adrenoleucodystrophy	Is a	Adrenal cortical hypofunction	false	Inferred relationship	Some
Adrenoleucodystrophy	Is a	Congenital anomaly of adrenal gland	false	Inferred relationship	Some
Adrenoleucodystrophy	Is a	Hereditary disorder of endocrine system	true	Inferred relationship	Some
Adrenoleucodystrophy	Is a	Reproductive system hereditary disorder	false	Inferred relationship	Some
Adrenoleucodystrophy	Occurrence	Congenital	true	Inferred relationship	Some	1
Adrenoleucodystrophy	Finding site	Adrenal cortex structure	true	Inferred relationship	Some	1
Adrenoleucodystrophy	Finding site	Entire endocrine gonad	false	Inferred relationship	Some
Adrenoleucodystrophy	Finding site	Adrenal cortex structure	false	Inferred relationship	Some
Adrenoleucodystrophy	Occurrence	Congenital	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Neonatal adrenoleucodystrophy	Is a	True	Adrenoleucodystrophy	Inferred relationship	Some
Acyl-CoA oxidase deficiency	Is a	False	Adrenoleucodystrophy	Inferred relationship	Some
Adolescent X-linked adrenoleukodystrophy	Is a	True	Adrenoleucodystrophy	Inferred relationship	Some
Childhood cerebral X-linked adrenoleukodystrophy	Is a	True	Adrenoleucodystrophy	Inferred relationship	Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
108634018	Adrenoleukodystrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
108635017	Adrenomyeloneuropathy	en	Synonym	Active	Case insensitive	SNOMED CT core
108637013	Bronze Schilder disease	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
108638015	Schilder-Addison complex	en	Synonym	Active	Case sensitive	SNOMED CT core
108639011	Siemerling-Creutzfeldt disease	en	Synonym	Active	Case sensitive	SNOMED CT core
1232670018	X-linked adrenoleucodystrophy	en	Synonym	Active	Case sensitive	SNOMED CT core
2154288010	Adrenoleucodystrophy	en	Synonym	Active	Case insensitive	SNOMED CT core
2957107010	ALD - adrenoleukodystrophy	en	Synonym	Active	Case sensitive	SNOMED CT core
4637154010	X-linked adrenoleukodystrophy	en	Synonym	Active	Case sensitive	SNOMED CT core
804886014	Adrenoleukodystrophy (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core