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15228007: Atrophia bulborum hereditaria (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
25843016 Atrophia bulborum hereditaria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
25844010 Norrie's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
25845011 Oligophrenia microphthalmus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
741991012 Atrophia bulborum hereditaria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
25843016 Atrophia bulborum hereditaria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
25843016 Atrophia bulborum hereditaria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
25844010 Norrie's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
25845011 Oligophrenia microphthalmus en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
25845011 Oligophrenia microphthalmus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
741991012 Atrophia bulborum hereditaria (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
741991012 Atrophia bulborum hereditaria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3421611001000115 Norrie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
66111000077119 atrophie bulbaire héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
66111000077119 atrophie bulbaire héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3421611001000115 Norrie-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
Atrophia bulborum hereditaria Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Multisystem disorder M-N false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Retinal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Finding site Nervous system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophia bulborum hereditaria Associated morphology Atrophy false Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophia bulborum hereditaria Finding site Retinal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophia bulborum hereditaria Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Degeneration of retina (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a trouble multisytémique false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Retina atrophic false Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Is a Atrophic retina (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Atrophia bulborum hereditaria Associated morphology Atrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophia bulborum hereditaria Finding site Retinal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Atrophia bulborum hereditaria Is a X-linked recessive hereditary disease true 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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