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25792000: Kearns-Sayre syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
43223013 Kearns-Sayre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
756150016 Kearns-Sayre syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1224922018 Kearns-Sayre mitochondrial cytopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1224923011 Mitochondrial ocular myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1224924017 KSS - Kearns-Sayre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755650016 Oculocraniosomatic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
43223013 Kearns-Sayre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
756150016 Kearns-Sayre syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
756150016 Kearns-Sayre syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1224922018 Kearns-Sayre mitochondrial cytopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1224922018 Kearns-Sayre mitochondrial cytopathy en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1224923011 Mitochondrial ocular myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1224923011 Mitochondrial ocular myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1224924017 KSS - Kearns-Sayre syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1224924017 KSS - Kearns-Sayre syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3755650016 Oculocraniosomatic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3419131001000113 Kearns-Sayre-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
885691000172117 syndrome de Kearns-Sayre fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
885691000172117 syndrome de Kearns-Sayre fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3419131001000113 Kearns-Sayre-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained 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 (core metadata concept)
Kearns-Sayre syndrome Is a Disorder of pyruvate metabolism and mitochondrial respiratory chain (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Is a Congenital anomaly of skeletal muscle (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Is a Mitochondrial cytopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Is a Disease of eye false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Kearns-Sayre syndrome Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Is a Hereditary disorder of the visual system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Is a Degenerative disorder of musculoskeletal system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Is a Secondary pigmentary retinal degeneration false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Kearns-Sayre syndrome Associated morphology Pigmentary degeneration false Inferred relationship Existential restriction modifier (core metadata concept) 1
Kearns-Sayre syndrome Is a Disorder of eye proper (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Kearns-Sayre syndrome Finding site Eye structure false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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