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765135003: Primary essential cutis verticis gyrata (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3657135011 Primary essential cutis verticis gyrata (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3657136012 Primary essential cutis verticis gyrata en Synonym Active Case insensitive SNOMED CT core
3657137015 A rare progressive dermis disorder with characteristics of thickening of the scalp resulting in redundancy of skin which gives rise to folds and grooves that give the scalp a cerebriform appearance. Folds cannot be corrected by pressure or traction and typically are symmetric and extend anteroposteriorly from vertex to occiput and/or transversely in occipital region. Additional features may include mild subungual hyperkeratosis and distal onycholysis of the nail plates of the great toes. It is not associated with neurological and ophthalmological changes or with secondary causes. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary essential cutis verticis gyrata Associated morphology Degenerative abnormality true Inferred relationship Some 1
Primary essential cutis verticis gyrata Associated morphology Degeneration false Inferred relationship Some 1
Primary essential cutis verticis gyrata Is a Cutis verticis gyrata true Inferred relationship Some
Primary essential cutis verticis gyrata Finding site Skin structure of scalp true Inferred relationship Some 1

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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