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15228007: Atrophia bulborum hereditaria (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
25843016 Atrophia bulborum hereditaria en Synonym Active Entire term case insensitive SNOMED CT core module
25844010 Norrie's disease en Synonym Active Entire term case sensitive SNOMED CT core module
25845011 Oligophrenia microphthalmus en Synonym Active Entire term case insensitive SNOMED CT core module
741991012 Atrophia bulborum hereditaria (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Atrophia bulborum hereditaria Is a Multisystem disorder M-N false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Retinal disorder false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Finding site Structure of nervous system false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Atrophia bulborum hereditaria Associated morphology Atrophy false Inferred relationship Existential restriction modifier 1
Atrophia bulborum hereditaria Finding site Retinal structure false Inferred relationship Existential restriction modifier 1
Atrophia bulborum hereditaria Occurrence Congenital false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Degeneration of retina false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Multisystem disorder false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Retina atrophic false Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Is a Atrophic retina true Inferred relationship Existential restriction modifier
Atrophia bulborum hereditaria Associated morphology Atrophy true Inferred relationship Existential restriction modifier 1
Atrophia bulborum hereditaria Finding site Retinal structure true Inferred relationship Existential restriction modifier 1
Atrophia bulborum hereditaria Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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