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41252002: Plexiform neurofibroma (morphologic abnormality)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
68811016 Plexiform neurofibroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
68812011 Plexiform neuroma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
778020017 Plexiform neurofibroma (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Plexiform neurofibroma Is a Neoplasm, benign false Inferred relationship Some
Plexiform neurofibroma Is a Nerve sheath tumor false Inferred relationship Some
Plexiform neurofibroma Is a Benign nerve sheath tumor - category false Inferred relationship Some
Plexiform neurofibroma Is a Benign neurofibroma true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Plexiform neurofibroma (disorder) Associated morphology True Plexiform neurofibroma Inferred relationship Some 1
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. Associated morphology True Plexiform neurofibroma Inferred relationship Some 1

This concept is not in any reference sets

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