45812003: Familial methionine malabsorption (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Kidney finding\Kidney disease\...

\Specific renal tubule transport defect\Familial methionine malabsorption

\Metabolic renal disease\Familial methionine malabsorption

\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Kidney finding\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Kidney finding\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Urinary system finding\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Finding of abdominopelvic segment of trunk\Urogenital finding\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Familial methionine malabsorption

\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneum\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Specific renal tubule transport defect\Familial methionine malabsorption
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Metabolic renal disease\Familial methionine malabsorption
\Disease\Metabolic disease\Organic acid metabolism disorder\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of sulfur-bearing amino acid metabolism\Familial methionine malabsorption
\Disease\Metabolic disease\Metabolic renal disease\Familial methionine malabsorption

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

Descriptions:

Id Description Lang Type Status Case? Module

1230267016 Oasthouse disease en Synonym Active Case insensitive SNOMED CT core

76397018 Familial methionine malabsorption en Synonym Active Case insensitive SNOMED CT core

76398011 Oast-house urine disease en Synonym Active Case sensitive SNOMED CT core

76399015 Methionine malabsorption syndrome en Synonym Active Case insensitive SNOMED CT core

76400010 Smith-Strang disease en Synonym Active Case sensitive SNOMED CT core

76401014 Beery-baby syndrome en Synonym Active Case insensitive SNOMED CT core

76402019 Oast-house disease en Synonym Active Case sensitive SNOMED CT core

783093016 Familial methionine malabsorption (disorder) en Fully specified name Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial methionine malabsorption	Is a	Metabolic renal disease	true	Inferred relationship	Some
Familial methionine malabsorption	Is a	Specific renal tubule transport defect	true	Inferred relationship	Some
Familial methionine malabsorption	Is a	Hereditary disorder of the urinary system	false	Inferred relationship	Some
Familial methionine malabsorption	Is a	Disorder of sulfur-bearing amino acid metabolism	true	Inferred relationship	Some
Familial methionine malabsorption	Is a	Congenital anomaly of trunk	false	Inferred relationship	Some
Familial methionine malabsorption	Finding site	Kidney structure	true	Inferred relationship	Some	1
Familial methionine malabsorption	Occurrence	Congenital	false	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

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1230267016	Oasthouse disease	en	Synonym	Active	Case insensitive	SNOMED CT core
76397018	Familial methionine malabsorption	en	Synonym	Active	Case insensitive	SNOMED CT core
76398011	Oast-house urine disease	en	Synonym	Active	Case sensitive	SNOMED CT core
76399015	Methionine malabsorption syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
76400010	Smith-Strang disease	en	Synonym	Active	Case sensitive	SNOMED CT core
76401014	Beery-baby syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
76402019	Oast-house disease	en	Synonym	Active	Case sensitive	SNOMED CT core
783093016	Familial methionine malabsorption (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core