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722992006: Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3334102013 Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3334103015 Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Is a Congenital malformation of the meninges true Inferred relationship Existential restriction modifier
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Is a Communicating hydrocephalus true Inferred relationship Existential restriction modifier
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Is a Congenital absence false Inferred relationship Existential restriction modifier
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Associated morphology Dilatation true Inferred relationship Existential restriction modifier 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Finding site Structure of brain cerebrospinal fluid pathway true Inferred relationship Existential restriction modifier 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 3
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Finding site Structure of Pacchionian granulation false Inferred relationship Existential restriction modifier 3
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Finding site Structure of Pacchionian granulation true Inferred relationship Existential restriction modifier 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Associated morphology Agenesis true Inferred relationship Existential restriction modifier 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi Is a Congenital hydrocephalus 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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