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721297008: Galloway Mowat syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Evaluation finding\Measurement finding\...

\Finding of substance level\Finding of urine substance level\Urine substance level above reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\Finding of substance level\Finding of urine substance level\Urine protein outside reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\Finding of substance level\Finding of protein level\Finding of albumin level\Albumin below reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\Finding of substance level\Finding of protein level\Urine protein outside reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome

\Measurement finding outside reference range\Measurement finding above reference range\Urine substance level above reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\Measurement finding outside reference range\Measurement finding below reference range\Albumin below reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\Measurement finding outside reference range\Urine protein outside reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome

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

\Hereditary nephropathy\Galloway Mowat syndrome

\Disorder of renal parenchyma\Glomerular disease\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome

\Central nervous system finding\Disorder of the central nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Galloway Mowat syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Galloway Mowat syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Galloway Mowat syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Galloway Mowat syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Galloway Mowat syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Galloway Mowat syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Galloway Mowat syndrome
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Galloway Mowat syndrome
\Disease\Disorder of body system\Disorder of nervous system\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Galloway Mowat syndrome
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Galloway Mowat syndrome
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Hereditary nephropathy\Galloway Mowat syndrome
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Disorder of kidney and/or ureter\Kidney disease\Disorder of renal parenchyma\Glomerular disease\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Galloway Mowat syndrome
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Hereditary nephropathy\Galloway Mowat syndrome
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Disorder of renal parenchyma\Glomerular disease\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\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\Hereditary nephropathy\Galloway Mowat syndrome
\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\Disorder of renal parenchyma\Glomerular disease\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Galloway Mowat syndrome
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of the genitourinary system\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Galloway Mowat syndrome
\Disease\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Galloway Mowat syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Galloway Mowat syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Galloway Mowat syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Galloway Mowat syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system\Disorder of neuronal migration and differentiation\Galloway Mowat syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3326229017 Galloway Mowat syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3326230010 Galloway Mowat syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

3326231014 Galloway syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

3326232019 Microcephaly, hiatus hernia, nephrotic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

3332175012 Nephrosis, neuronal dysmigration syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Galloway Mowat syndrome	Is a	Congenital nephrotic syndrome	false	Inferred relationship	Existential restriction modifier
Galloway Mowat syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Existential restriction modifier
Galloway Mowat syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Galloway Mowat syndrome	Is a	Steroid-resistant nephrotic syndrome	true	Inferred relationship	Existential restriction modifier
Galloway Mowat syndrome	Is a	Disorder of neuronal migration and differentiation	true	Inferred relationship	Existential restriction modifier
Galloway Mowat syndrome	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Galloway Mowat syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Galloway Mowat syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Galloway Mowat syndrome	Finding site	Structure of central nervous system	false	Inferred relationship	Existential restriction modifier	2
Galloway Mowat syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Galloway Mowat syndrome	Finding site	Glomerulus structure	false	Inferred relationship	Existential restriction modifier	3
Galloway Mowat syndrome	Finding site	Glomerulus structure	true	Inferred relationship	Existential restriction modifier	2
Galloway Mowat syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Galloway Mowat syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Galloway Mowat syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Galloway Mowat syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Galloway Mowat syndrome	Finding site	Structure of central nervous system	true	Inferred relationship	Existential restriction modifier	1
Galloway Mowat syndrome	Is a	Hereditary nephropathy	true	Inferred relationship	Existential restriction modifier
Galloway Mowat syndrome	Interprets	Albumin measurement	true	Inferred relationship	Existential restriction modifier	4
Galloway Mowat syndrome	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	4
Galloway Mowat syndrome	Interprets	Measurement of protein in urine	true	Inferred relationship	Existential restriction modifier	3
Galloway Mowat syndrome	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier	3
Galloway Mowat syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3326229017	Galloway Mowat syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3326230010	Galloway Mowat syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3326231014	Galloway syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3326232019	Microcephaly, hiatus hernia, nephrotic syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3332175012	Nephrosis, neuronal dysmigration syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module