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1187305006: Partially involuting congenital hemangioma (disorder)


Status: current, Primitive. Date: 31-Jan 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4673271010 Partially involuting congenital hemangioma (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4673272015 Partially involuting congenital haemangioma en Synonym Active Case insensitive SNOMED CT core
4673273013 Partially involuting congenital hemangioma en Synonym Active Case insensitive SNOMED CT core
4673274019 A rare congenital haemangioma characterised by a superficial, red to violaceous lesion with overlying telangiectasia and a surrounding pale halo, which initially behaves like a rapidly involuting congenital haemangioma, beginning to involute shortly after birth. Involution is then aborted, and a residual tumour virtually indistinguishable from non-involuting congenital haemangioma remains. This lesion grows proportionally with the child and does not regress. en Definition Active Case sensitive SNOMED CT core
4673275018 A rare congenital hemangioma characterized by a superficial, red to violaceous lesion with overlying telangiectasia and a surrounding pale halo, which initially behaves like a rapidly involuting congenital hemangioma, beginning to involute shortly after birth. Involution is then aborted, and a residual tumor virtually indistinguishable from non-involuting congenital hemangioma remains. This lesion grows proportionally with the child and does not regress. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Partially involuting congenital haemangioma Is a Congenital haemangioma true Inferred relationship Some
Partially involuting congenital haemangioma Occurrence Congenital true Inferred relationship Some 1
Partially involuting congenital haemangioma Finding site Blood vessel structure true Inferred relationship Some 1
Partially involuting congenital haemangioma Associated morphology Benign haemangioma true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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