FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server  |   User: [n/a]

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 Reference Sets
25843016 Atrophia bulborum hereditaria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
25844010 Norrie's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
25845011 Oligophrenia microphthalmus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
741991012 Atrophia bulborum hereditaria (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
259081000052117 atrophia bulborum hereditaria sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophia bulborum hereditaria Is a X-linked hereditary disease true Inferred relationship Some
Atrophia bulborum hereditaria Is a Multisystem disorder M-N false Inferred relationship Some
Atrophia bulborum hereditaria Is a Congenital anomaly of eye false Inferred relationship Some
Atrophia bulborum hereditaria Is a Retinal disorder false Inferred relationship Some
Atrophia bulborum hereditaria Is a Hereditary disorder of nervous system false Inferred relationship Some
Atrophia bulborum hereditaria Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Atrophia bulborum hereditaria Finding site Structure of nervous system (body structure) false Inferred relationship Some
Atrophia bulborum hereditaria Associated morphology kongenital anomali false Inferred relationship Some 1
Atrophia bulborum hereditaria Associated morphology Atrophy false Inferred relationship Some 1
Atrophia bulborum hereditaria Finding site Retinal structure false Inferred relationship Some 1
Atrophia bulborum hereditaria Occurrence Congenital false Inferred relationship Some
Atrophia bulborum hereditaria Is a Degeneration of retina false Inferred relationship Some
Atrophia bulborum hereditaria Is a multisystemsjukdom false Inferred relationship Some
Atrophia bulborum hereditaria Is a Retina atrophic false Inferred relationship Some
Atrophia bulborum hereditaria Is a Atrophic retina (disorder) true Inferred relationship Some
Atrophia bulborum hereditaria Associated morphology Atrophy true Inferred relationship Some 1
Atrophia bulborum hereditaria Finding site Retinal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start