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403818001: Plexiform neurofibroma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771744013 Plexiform neurofibroma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1782825018 Plexiform neurofibroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5264901000241116 neurofibrome plexiforme fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Plexiform neurofibroma (disorder) Is a Neurofibromatosis type 1 false Inferred relationship Some
Plexiform neurofibroma (disorder) Finding site Structure of nervous system (body structure) false Inferred relationship Some
Plexiform neurofibroma (disorder) Finding site Subcutaneous tissue structure false Inferred relationship Some 3
Plexiform neurofibroma (disorder) Associated morphology anomalie congénitale false Inferred relationship Some
Plexiform neurofibroma (disorder) Finding site Structure of skin region false Inferred relationship Some 1
Plexiform neurofibroma (disorder) Associated morphology Hamartoma false Inferred relationship Some
Plexiform neurofibroma (disorder) Associated morphology Pigment deposition false Inferred relationship Some 3
Plexiform neurofibroma (disorder) Associated morphology Plexiform neurofibroma true Inferred relationship Some 1
Plexiform neurofibroma (disorder) Finding site Skin structure false Inferred relationship Some 2
Plexiform neurofibroma (disorder) Finding site Skin structure false Inferred relationship Some 1
Plexiform neurofibroma (disorder) Associated morphology Neurofibroma, no International Classification of Diseases for Oncology subtype false Inferred relationship Some 3
Plexiform neurofibroma (disorder) Occurrence Congenital false Inferred relationship Some
Plexiform neurofibroma (disorder) Associated morphology Neurofibromatosis false Inferred relationship Some 2
Plexiform neurofibroma (disorder) Associated morphology Dysplasia false Inferred relationship Some 1
Plexiform neurofibroma (disorder) Finding site Skin structure false Inferred relationship Some 3
Plexiform neurofibroma (disorder) Is a Benign neoplasm of nerve sheath origin (disorder) false Inferred relationship Some
Plexiform neurofibroma (disorder) Is a Neurofibroma (disorder) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Painful orbital and systemic neurofibromas-marfanoid habitus syndrome is a rare, benign, peripheral nerve sheath tumor disorder characterized by multiple, painful, mucin-rich plexiform neurofibromas located in the orbits, cranium, large spinal nerves and mucosa, associated with a marfanoid habitus, enlarged corneal nerves, congenital neuronal migration anomalies and facial dysmorphism which includes ptosis, proptosis, prominent nose, full lips, gingival hyperplasia, and multiple subcutaneous and submucosal nodules in the lips and sublingual zone. Is a True Plexiform neurofibroma (disorder) Inferred relationship Some

This concept is not in any reference sets

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