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703528008: Cutis gyrata syndrome of Beare and Stevenson (disorder)


Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3009081015 Cutis gyrata syndrome of Beare and Stevenson en Synonym Active Initial character case insensitive SNOMED CT core
3009171017 Beare-Stevenson cutis gyrata syndrome en Synonym Active Case sensitive SNOMED CT core
3009385019 Cutis gyrata syndrome of Beare and Stevenson (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
4029018019 Cutis gyrata, acanthosis nigricans, craniosynostosis syndrome en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cutis gyrata syndrome of Beare and Stevenson Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Cutis gyrata syndrome of Beare and Stevenson Finding site Skin structure true Inferred relationship Some 1
Cutis gyrata syndrome of Beare and Stevenson Pathological process Pathological developmental process true Inferred relationship Some 2
Cutis gyrata syndrome of Beare and Stevenson Occurrence Congenital true Inferred relationship Some 1
Cutis gyrata syndrome of Beare and Stevenson Pathological process Pathological developmental process true Inferred relationship Some 1
Cutis gyrata syndrome of Beare and Stevenson Is a Inherited disorder of keratinisation true Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Is a Acanthosis nigricans true Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Has interpretation Abnormal true Inferred relationship Some 3
Cutis gyrata syndrome of Beare and Stevenson Interprets Keratinisation true Inferred relationship Some 3
Cutis gyrata syndrome of Beare and Stevenson Is a Developmental hereditary disorder true Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Is a Congenital anomaly of skin true Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Is a Hereditary disorder of the integument false Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Is a Craniosynostosis syndrome true Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Occurrence Congenital true Inferred relationship Some 2
Cutis gyrata syndrome of Beare and Stevenson Occurrence Congenital false Inferred relationship Some 3
Cutis gyrata syndrome of Beare and Stevenson Associated morphology Congenital premature fusion true Inferred relationship Some 2
Cutis gyrata syndrome of Beare and Stevenson Finding site Joint structure of suture of skull true Inferred relationship Some 2
Cutis gyrata syndrome of Beare and Stevenson Associated morphology Developmental abnormality false Inferred relationship Some 3
Cutis gyrata syndrome of Beare and Stevenson Finding site Skin structure false Inferred relationship Some 3
Cutis gyrata syndrome of Beare and Stevenson Is a Inherited disorder of connective tissue false Inferred relationship Some
Cutis gyrata syndrome of Beare and Stevenson Finding site Bone structure of cranium false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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