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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 (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

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 (core metadata concept) SNOMED CT core
3334103015 Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi en Synonym (core metadata concept) 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
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Is a Congenital malformation of the meninges true Inferred relationship Some
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Is a Communicating hydrocephalus true Inferred relationship Some
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Is a Congenital absence false Inferred relationship Some
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Associated morphology Dilatation true Inferred relationship Some 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Occurrence Congenital true Inferred relationship Some 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Finding site Brain cerebrospinal fluid pathway true Inferred relationship Some 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 3
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Occurrence Congenital false Inferred relationship Some 3
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Finding site Pacchionian granulation false Inferred relationship Some 3
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Occurrence Congenital true Inferred relationship Some 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Is a Congenital anomaly of brain false Inferred relationship Some
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Finding site Pacchionian granulation true Inferred relationship Some 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Associated morphology Agenesis (morphologic abnormality) true Inferred relationship Some 1
Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder) Is a Congenital hydrocephalus true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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