60392001: Angiofibroma, no International Classification of Diseases for Oncology subtype (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

100337019 Angiofibroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

100339016 Juvenile angiofibroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

100340019 Nasopharyngeal angiofibroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

198954016 Involuting nevus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

198955015 Giant cell angiofibroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

198957011 Cellular angiofibroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

498724016 Involuting naevus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

2765123014 Angiofibroma, no ICD-O subtype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2973156011 Angiofibroma, no International Classification of Diseases for Oncology subtype (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

2973267015 Angiofibroma, no International Classification of Diseases for Oncology subtype en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Angiofibroma, no International Classification of Diseases for Oncology subtype	Is a	Neoplasm, benign	false	Inferred relationship	Some
Angiofibroma, no International Classification of Diseases for Oncology subtype	Is a	Blood vessel tumor	false	Inferred relationship	Some
Angiofibroma, no International Classification of Diseases for Oncology subtype	Is a	Benign blood vessel neoplasm (morphologic abnormality)	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Pearly penile papules	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	1
Fibrous skin tumor of tuberous sclerosis	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	1
Angiofibroma	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	1
Fibrous papule of face	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	1
Fibrous papule of nose	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	1
Angiofibroma	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	1
Angiofibroma of nasopharynx	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	1
Juvenile nasopharyngeal angiofibroma (JNA) is a rare and benign but locally aggressive fibrovascular tumor arising from the posterolateral wall of the nasopharynx, which affects mainly young and adolescent males (onset usually occurring between 7-19 years of age) and that presents as a mass in the nasopharynx and nasal cavity, leading to manifestations such as nasal obstruction, epistaxis, profound facial swelling, proptosis or diplopia. Although slowly progressive, it has a high rate of recurrence and sometimes invades adjacent structures.	Associated morphology	False	Angiofibroma, no International Classification of Diseases for Oncology subtype	Inferred relationship	Some	2

Reference Sets

Concept inactivation indicator reference set

REPLACED BY association reference set (foundation metadata concept)