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778044004: Primary non-essential cutis verticis gyrata (disorder)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3737487011 Primary non-essential cutis verticis gyrata (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3737488018 Primary non-essential cutis verticis gyrata en Synonym Active Case insensitive SNOMED CT core
3737489014 A rare genetic dermis disorder with characteristics of slowly progressive thickening of the scalp, which becomes raised and forms ridges and furrows with symmetrical distribution resembling the cerebral gyri and cannot be flattened by traction or pressure, associated with ophthalmologic (for example congenital cataract) and/or neurological abnormalities (for example intellectual disability, epilepsy, microcephaly, encephalopathy). en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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