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722381004: Congenital cataract, nephropathy, encephalopathy syndrome (disorder)

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
3331765016 Congenital cataract, nephropathy, encephalopathy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3331766015 Congenital cataract, nephropathy, encephalopathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3331767012 Crome syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital cataract, nephropathy, encephalopathy syndrome Is a Congenital cataract true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Disorder of brain false Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Renal tubular disorder true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Short stature disorder true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Necrosis of cortex of kidney true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Hereditary nephropathy true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Associated morphology Necrosis false Inferred relationship Existential restriction modifier 3
Congenital cataract, nephropathy, encephalopathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Congenital cataract, nephropathy, encephalopathy syndrome Finding site Renal tubule structure false Inferred relationship Existential restriction modifier 3
Congenital cataract, nephropathy, encephalopathy syndrome Associated morphology Congenital cataract false Inferred relationship Existential restriction modifier 4
Congenital cataract, nephropathy, encephalopathy syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Congenital cataract, nephropathy, encephalopathy syndrome Finding site Structure of lens of eye false Inferred relationship Existential restriction modifier 4
Congenital cataract, nephropathy, encephalopathy syndrome Finding site Structure of lens of eye true Inferred relationship Existential restriction modifier 3
Congenital cataract, nephropathy, encephalopathy syndrome Is a Congenital anomaly of the kidney true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Congenital cataract, nephropathy, encephalopathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Congenital cataract, nephropathy, encephalopathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Congenital cataract, nephropathy, encephalopathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenital cataract, nephropathy, encephalopathy syndrome Finding site Renal tubule structure true Inferred relationship Existential restriction modifier 1
Congenital cataract, nephropathy, encephalopathy syndrome Associated morphology Necrosis true Inferred relationship Existential restriction modifier 1
Congenital cataract, nephropathy, encephalopathy syndrome Finding site Brain structure true Inferred relationship Existential restriction modifier 2
Congenital cataract, nephropathy, encephalopathy syndrome Associated morphology Cataract false Inferred relationship Existential restriction modifier 3
Congenital cataract, nephropathy, encephalopathy syndrome Associated morphology Abnormally opaque structure true Inferred relationship Existential restriction modifier 3
Congenital cataract, nephropathy, encephalopathy syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 4
Congenital cataract, nephropathy, encephalopathy syndrome Is a Traumatic or nontraumatic brain injury true Inferred relationship Existential restriction modifier
Congenital cataract, nephropathy, encephalopathy syndrome Is a Injury of lens true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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