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723449004: Pierson 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\Pierson syndrome
\Finding of substance level\Finding of urine substance level\Urine protein outside reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Pierson syndrome
\Finding of substance level\Finding of protein level\Finding of albumin level\Albumin below reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Pierson syndrome
\Finding of substance level\Finding of protein level\Urine protein outside reference range\Nephrotic syndrome\Steroid-resistant nephrotic syndrome\Pierson syndrome

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

\Hereditary nephropathy\Pierson syndrome

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

\Finding of head and neck region\Head finding\...

\Finding of head region\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Pierson syndrome
\Finding of head region\Globe finding\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Pierson syndrome

\Disorder of head\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Pierson syndrome
\Disorder of head\Congenital anomaly of head\Congenital anomaly of eye\Pierson syndrome

\Eye / vision finding\Globe finding\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Pierson syndrome
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Pierson syndrome
\Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system\Pierson syndrome
\Eye / vision finding\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Pierson syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Pierson syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Pierson syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Pierson syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Pierson syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Pierson syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the urinary system\Hereditary nephropathy\Pierson syndrome
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Pierson syndrome
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Pierson syndrome
\Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Pierson 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\Pierson 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\Pierson syndrome
\Disease\Disorder of body system\Disorder of the genitourinary system\Disorder of the urinary system\Hereditary disorder of the urinary system\Hereditary nephropathy\Pierson syndrome
\Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of retroperitoneal compartment\Kidney disease\Hereditary nephropathy\Pierson 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\Pierson 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\Pierson 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\Pierson 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\Pierson syndrome
\Disease\Disorder of head\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Pierson syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of eye\Pierson syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Pierson syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Pierson syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Pierson syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Pierson syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Pierson syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

3424664019 Pierson syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

3424665018 Pierson syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

3424666017 Microcoria and congenital nephrosis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pierson syndrome	Is a	Congenital anomaly of eye	true	Inferred relationship	Existential restriction modifier
Pierson syndrome	Is a	Congenital nephrotic syndrome	false	Inferred relationship	Existential restriction modifier
Pierson syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Pierson syndrome	Is a	Steroid-resistant nephrotic syndrome	true	Inferred relationship	Existential restriction modifier
Pierson syndrome	Is a	Hereditary disorder of the visual system	true	Inferred relationship	Existential restriction modifier
Pierson syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Pierson syndrome	Finding site	Glomerulus structure	true	Inferred relationship	Existential restriction modifier	2
Pierson syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Pierson syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Pierson syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	2
Pierson syndrome	Finding site	Glomerulus structure	false	Inferred relationship	Existential restriction modifier	3
Pierson syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Pierson syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Pierson syndrome	Finding site	Structure of eye proper	true	Inferred relationship	Existential restriction modifier	1
Pierson syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Pierson syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Pierson syndrome	Is a	Hereditary nephropathy	true	Inferred relationship	Existential restriction modifier
Pierson syndrome	Interprets	Albumin measurement	true	Inferred relationship	Existential restriction modifier	4
Pierson syndrome	Has interpretation	Below reference range	true	Inferred relationship	Existential restriction modifier	4
Pierson syndrome	Interprets	Measurement of protein in urine	true	Inferred relationship	Existential restriction modifier	3
Pierson syndrome	Has interpretation	Above reference range	true	Inferred relationship	Existential restriction modifier	3
Pierson 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
3424664019	Pierson syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3424665018	Pierson syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3424666017	Microcoria and congenital nephrosis syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module