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25792000: Kearns-Sayre syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
43223013 Kearns-Sayre syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
756150016 Kearns-Sayre syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1224922018 Kearns-Sayre mitochondrial cytopathy en Synonym Active Entire term case sensitive SNOMED CT core module
1224923011 Mitochondrial ocular myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
1224924017 KSS - Kearns-Sayre syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3755650016 Oculocraniosomatic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Kearns-Sayre syndrome Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Disorder of pyruvate metabolism and mitochondrial respiratory chain true Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Congenital anomaly of skeletal muscle false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Mitochondrial cytopathy true Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Disease of eye false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Finding site Structure of eye proper false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Kearns-Sayre syndrome Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Degenerative disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Is a Secondary pigmentary retinal degeneration false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier 1
Kearns-Sayre syndrome Associated morphology Pigmentary degeneration false Inferred relationship Existential restriction modifier 1
Kearns-Sayre syndrome Is a Disorder of eye proper false Inferred relationship Existential restriction modifier
Kearns-Sayre syndrome Finding site Structure of eye proper false 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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