236383002: Familial mesangial sclerosis (disorder)

\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis

\Urine finding\Finding of urine substance level\...

\Urine substance level above reference range (finding)\Proteinuria\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis

\Urine protein outside reference range (finding)\Proteinuria\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis

\Procedure related finding\Evaluation finding\Measurement finding\...

\Finding of substance level (finding)\Finding of urine substance level\Urine substance level above reference range (finding)\Proteinuria\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Finding of substance level (finding)\Finding of urine substance level\Urine protein outside reference range (finding)\Proteinuria\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Finding of substance level (finding)\Finding of protein level (finding)\Albumin level - finding\Albumin below reference range (finding)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Finding of substance level (finding)\Finding of protein level (finding)\Urine protein outside reference range (finding)\Proteinuria\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis

\Measurement finding outside reference range\Measurement finding above reference range (finding)\Urine substance level above reference range (finding)\Proteinuria\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Measurement finding outside reference range\Measurement finding below reference range (finding)\Albumin below reference range (finding)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Measurement finding outside reference range\Urine protein outside reference range (finding)\Proteinuria\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disorder of genitourinary system\Familial mesangial sclerosis
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Inflammatory disorder of genitourinary system\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of body system\Disease of the genitourinary system (disorder)\Disorder of urinary system\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disorder of genitourinary system\Familial mesangial sclerosis
\Disease\Inflammatory disorder (disorder)\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Congenital anomaly of lower trunk\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of retroperitoneal compartment (disorder)\Kidney disease\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of kidney and/or ureter\Kidney disease\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of kidney and/or ureter\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of kidney and/or ureter\Kidney disease\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Disorder of kidney and/or ureter\Kidney disease\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of abdomen\Congenital anomaly of abdomen\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Inflammatory disorder of genitourinary system\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Disorder of renal parenchyma (disorder)\Glomerular disease\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Protein-losing nephropathy (disorder)\Nephrotic syndrome\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of urinary system\Disorder of kidney and/or ureter\Kidney disease\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy (disorder)\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Disorder of abdominopelvic segment of trunk\Disease of the genitourinary system (disorder)\Disorder of urinary system\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Disorder of trunk (disorder)\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital abnormality of lower limb and pelvic girdle\Congenital anomaly of lower trunk\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Congenital anomaly of abdomen\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of trunk\Congenital anomaly of lower trunk\Genitourinary congenital anomalies\Congenital malformation of the urinary system\Congenital anomaly of the kidney\Congenital nephrotic syndrome\Familial mesangial sclerosis

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial mesangial sclerosis	Is a	Congenital anomaly of the urinary tract	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Is a	Hereditary nephritis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Is a	Congenital nephrotic syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Finding site	Kidney structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial mesangial sclerosis	Finding site	Glomerulus structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial mesangial sclerosis	Finding site	Urinary system structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial mesangial sclerosis	Associated morphology	inflammation chronique	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial mesangial sclerosis	Course	Multiple superficial injuries of lower leg	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Course	Chronic (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial mesangial sclerosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Associated morphology	Basement membrane alteration	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Has definitional manifestation	Blood in urine	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Finding site	Glomerulus structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial mesangial sclerosis	Is a	Inflammatory disorder of genitourinary system	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Is a	Inflammation of specific body organs	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Finding site	Kidney structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial mesangial sclerosis	Is a	Congenital nephritis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Is a	Chronic disease of genitourinary system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Is a	Chronic inflammatory disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Course	Chronic (qualifier value)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Finding site	Kidney structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial mesangial sclerosis	Associated morphology	inflammation chronique	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Familial mesangial sclerosis	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial mesangial sclerosis	Finding site	Glomerulus structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial mesangial sclerosis	Is a	Inflammation of specific body organs	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Is a	Inflammatory disorder of genitourinary system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial mesangial sclerosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial mesangial sclerosis	Finding site	Glomerulus structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial mesangial sclerosis	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial mesangial sclerosis	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial mesangial sclerosis	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Familial mesangial sclerosis	Interprets	Albumin measurement (procedure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial mesangial sclerosis	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial mesangial sclerosis	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Familial mesangial sclerosis	Interprets	Measurement of protein in urine (procedure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Familial mesangial sclerosis	Associated morphology	Chronic inflammatory morphology (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
354339017	Familial mesangial sclerosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
624968019	Familial mesangial sclerosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
354339017	Familial mesangial sclerosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
354339017	Familial mesangial sclerosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
624968019	Familial mesangial sclerosis (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
624968019	Familial mesangial sclerosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6220871000241116	sclérose mésangiale familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6220871000241116	sclérose mésangiale familiale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module