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


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3009081015 Cutis gyrata syndrome of Beare and Stevenson en Synonym Active Only initial character case insensitive SNOMED CT core module
3009171017 Beare-Stevenson cutis gyrata syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3009385019 Cutis gyrata syndrome of Beare and Stevenson (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4029018019 Cutis gyrata, acanthosis nigricans, craniosynostosis syndrome 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
Cutis gyrata syndrome of Beare and Stevenson Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Is a Congenital anomaly of skin true Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Is a Craniosynostosis syndrome true Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Cutis gyrata syndrome of Beare and Stevenson Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Cutis gyrata syndrome of Beare and Stevenson Associated morphology Congenital premature fusion true Inferred relationship Existential restriction modifier 2
Cutis gyrata syndrome of Beare and Stevenson Finding site Joint structure of suture of skull true Inferred relationship Existential restriction modifier 2
Cutis gyrata syndrome of Beare and Stevenson Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Cutis gyrata syndrome of Beare and Stevenson Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Cutis gyrata syndrome of Beare and Stevenson Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Finding site Bone structure of cranium false Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Cutis gyrata syndrome of Beare and Stevenson Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Cutis gyrata syndrome of Beare and Stevenson Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Cutis gyrata syndrome of Beare and Stevenson Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Cutis gyrata syndrome of Beare and Stevenson Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Cutis gyrata syndrome of Beare and Stevenson Is a Inherited disorder of keratinization true Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Is a Acanthosis nigricans true Inferred relationship Existential restriction modifier
Cutis gyrata syndrome of Beare and Stevenson Has interpretation Abnormal true Inferred relationship Existential restriction modifier 3
Cutis gyrata syndrome of Beare and Stevenson Interprets Keratinization, function true Inferred relationship Existential restriction modifier 3
Cutis gyrata syndrome of Beare and Stevenson Is a Developmental hereditary disorder 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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