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15228007: Atrophia bulborum hereditaria (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
25843016 Atrophia bulborum hereditaria en Synonym Active Case insensitive SNOMED CT core
25844010 Norrie's disease en Synonym Active Case sensitive SNOMED CT core
25845011 Oligophrenia microphthalmus en Synonym Active Case insensitive SNOMED CT core
741991012 Atrophia bulborum hereditaria (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophia bulborum hereditaria Is a X-linked recessive hereditary disease true Inferred relationship Some
Atrophia bulborum hereditaria Is a Degeneration of retina false Inferred relationship Some
Atrophia bulborum hereditaria Is a Multisystem disorder false Inferred relationship Some
Atrophia bulborum hereditaria Is a X-linked hereditary disease false 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 true Inferred relationship Some
Atrophia bulborum hereditaria Is a Retina atrophic false Inferred relationship Some
Atrophia bulborum hereditaria Is a Atrophic retina 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
Atrophia bulborum hereditaria Finding site Structure of nervous system false Inferred relationship Some
Atrophia bulborum hereditaria Associated morphology Congenital anomaly 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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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