65389002: Adrenoleukodystrophy (disorder)

SNOMED CT Concept\Clinical finding\...

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

\Hypoadrenalism\Adrenal cortical hypofunction\Adrenoleukodystrophy

\Disorder of adrenal cortex\Adrenal cortical hypofunction\Adrenoleukodystrophy

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Hypoadrenalism\Adrenal cortical hypofunction\Adrenoleukodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal cortical hypofunction\Adrenoleukodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Disorder of adrenal gland\Hypoadrenalism\Adrenal cortical hypofunction\Adrenoleukodystrophy
\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 cortical hypofunction\Adrenoleukodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Hypoadrenalism\Adrenal cortical hypofunction\Adrenoleukodystrophy
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal cortical hypofunction\Adrenoleukodystrophy
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Hypoadrenalism\Adrenal cortical hypofunction\Adrenoleukodystrophy
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Disorder of adrenal gland\Disorder of adrenal cortex\Adrenal cortical hypofunction\Adrenoleukodystrophy

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

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

Descriptions:

Id Description Lang Type Status Case? Module

108634018 Adrenoleukodystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

108635017 Adrenomyeloneuropathy en Synonym Active Entire term case insensitive SNOMED CT core module

108637013 Bronze Schilder disease en Synonym Active Only initial character case insensitive SNOMED CT core module

108638015 Schilder-Addison complex en Synonym Active Entire term case sensitive SNOMED CT core module

108639011 Siemerling-Creutzfeldt disease en Synonym Active Entire term case sensitive SNOMED CT core module

804886014 Adrenoleukodystrophy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

1232670018 X-linked adrenoleucodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module

2154288010 Adrenoleucodystrophy en Synonym Active Entire term case insensitive SNOMED CT core module

2957107010 ALD - adrenoleukodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module

4637154010 X-linked adrenoleukodystrophy en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Neonatal adrenoleukodystrophy	Is a	True	Adrenoleukodystrophy	Inferred relationship	Existential restriction modifier
Acyl-coenzyme A oxidase deficiency	Is a	False	Adrenoleukodystrophy	Inferred relationship	Existential restriction modifier
Adolescent X-linked adrenoleukodystrophy	Is a	True	Adrenoleukodystrophy	Inferred relationship	Existential restriction modifier
Childhood cerebral X-linked adrenoleukodystrophy	Is a	True	Adrenoleukodystrophy	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

Back to Start

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