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253232000: Aniridia type 2 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
377135012 AN2 en Synonym Active Case sensitive SNOMED CT core
377136013 Aniridia type 2 en Synonym Active Case insensitive SNOMED CT core
643966017 Aniridia type 2 (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
Aniridia type 2 Pathological process Pathological developmental process true Inferred relationship Some 1
Aniridia type 2 Occurrence Congenital true Inferred relationship Some 1
Aniridia type 2 Associated morphology Absence true Inferred relationship Some 1
Aniridia type 2 Finding site Iridial and/or ciliary structure false Inferred relationship Some 1
Aniridia type 2 Associated morphology Congenital absence false Inferred relationship Some 1
Aniridia type 2 Finding site Iris structure false Inferred relationship Some 1
Aniridia type 2 Associated morphology Congenital absence false Inferred relationship Some 1
Aniridia type 2 Finding site Iris structure true Inferred relationship Some 1
Aniridia type 2 Occurrence Congenital false Inferred relationship Some 2
Aniridia type 2 Finding site Iris structure false Inferred relationship Some 2
Aniridia type 2 Associated morphology Congenital absence false Inferred relationship Some 2
Aniridia type 2 Associated morphology Developmental abnormality false Inferred relationship Some 1
Aniridia type 2 Finding site Structure of nervous system false Inferred relationship Some
Aniridia type 2 Occurrence Congenital false Inferred relationship Some
Aniridia type 2 Finding site Iridial and/or ciliary structure false Inferred relationship Some 3
Aniridia type 2 Is a Congenital aniridia true 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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