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1162826002: Split spinal cord malformation type I (disorder)


Status: current, 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
4591647011 Split spinal cord malformation type 1 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4591648018 Split spinal cord malformation type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591649014 Split spinal cord malformation type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
4591650014 A rare, neural tube defect characterized by localized longitudinal division of the spinal cord with an interposed osseous, cartilaginous or fibrous septum and double dural sac, typically occurring at the thoracic or lumbar level. Local vertebral segmental defects, syringomyelia, meningocele and intraspinal tumors may be associated. Variable clinical presentation includes pain, scoliosis, asymmetry and weakness of the lower limbs, neurological deficits, sphincter dysfunction, and various cutaneous abnormalities overlying the spine, such as hypertrichosis, dimple, hemangioma, subcutaneous mass or pigmented nevus. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4591652018 A rare, neural tube defect characterised by localised longitudinal division of the spinal cord with an interposed osseous, cartilaginous or fibrous septum and double dural sac, typically occurring at the thoracic or lumbar level. Local vertebral segmental defects, syringomyelia, meningocele and intraspinal tumours may be associated. Variable clinical presentation includes pain, scoliosis, asymmetry and weakness of the lower limbs, neurological deficits, sphincter dysfunction, and various cutaneous abnormalities overlying the spine, such as hypertrichosis, dimple, haemangioma, subcutaneous mass or pigmented naevus. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Split spinal cord malformation type I (disorder) est un(e) (attribut) Split spinal cord malformation (disorder) true Inferred relationship Some
Split spinal cord malformation type I (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Split spinal cord malformation type I (disorder) localisation d'une constatation (attribut) Structure of arch of vertebra true Inferred relationship Some 1
Split spinal cord malformation type I (disorder) morphologie associée (attribut) Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 1
Split spinal cord malformation type I (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Split spinal cord malformation type I (disorder) survenue (attribut) congénital true Inferred relationship Some 2
Split spinal cord malformation type I (disorder) localisation d'une constatation (attribut) Neural tube structure true Inferred relationship Some 2
Split spinal cord malformation type I (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 2
Split spinal cord malformation type I (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Split spinal cord malformation type I (disorder) survenue (attribut) congénital true Inferred relationship Some 3
Split spinal cord malformation type I (disorder) localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 3
Split spinal cord malformation type I (disorder) morphologie associée (attribut) Congenital septation true Inferred relationship Some 3
Split spinal cord malformation type I (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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