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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
66111000077119 atrophie bulbaire héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
688261000077116 atrophie bulbaire héréditaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
741991012 Atrophia bulborum hereditaria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophia bulborum hereditaria est un(e) (attribut) X-linked recessive hereditary disease true Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) dégénérescence de la rétine false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) Multisystem disorder (disorder) false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) X-linked hereditary disease false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) Multisystem disorder M-N (navigational concept) false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) Congenital anomaly of eye false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) trouble rétinien (trouble) false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) Hereditary disorder of nervous system false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) Hereditary disorder of the visual system true Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) Retina atrophic false Inferred relationship Some
Atrophia bulborum hereditaria est un(e) (attribut) Atrophic retina (disorder) true Inferred relationship Some
Atrophia bulborum hereditaria morphologie associée (attribut) atrophie (anomalie morphologique) true Inferred relationship Some 1
Atrophia bulborum hereditaria localisation d'une constatation (attribut) structure de la rétine true Inferred relationship Some 1
Atrophia bulborum hereditaria localisation d'une constatation (attribut) système nerveux false Inferred relationship Some
Atrophia bulborum hereditaria morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Atrophia bulborum hereditaria morphologie associée (attribut) atrophie (anomalie morphologique) false Inferred relationship Some 1
Atrophia bulborum hereditaria localisation d'une constatation (attribut) structure de la rétine false Inferred relationship Some 1
Atrophia bulborum hereditaria survenue (attribut) congénital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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