1162826002: Split spinal cord malformation type I (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Finding of back (finding)\Finding of spinal region\Disorder of spinal region (disorder)\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Finding of spinal region\Disorder of spinal region (disorder)\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Finding of spinal region\Disorder of spinal region (disorder)\Disorder of vertebral column (disorder)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Finding of spinal region\Disorder of spinal region (disorder)\Spinal cord disorder (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Finding of spinal region\Finding of spinal cord (finding)\Spinal cord disorder (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Finding of spinal region\Vertebral column finding (finding)\Disorder of vertebral column (disorder)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Finding of spinal region\Vertebral column finding (finding)\Finding of vertebra (finding)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Disorder of back\Disorder of spinal region (disorder)\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Disorder of back\Disorder of spinal region (disorder)\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Disorder of back\Disorder of spinal region (disorder)\Disorder of vertebral column (disorder)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Disorder of back\Disorder of spinal region (disorder)\Spinal cord disorder (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Disorder of back\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Finding of back (finding)\Disorder of back\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Central nervous system finding\Finding of spinal cord (finding)\Spinal cord disorder (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Spinal cord disorder (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Musculoskeletal finding (finding)\Vertebral column finding (finding)\Disorder of vertebral column (disorder)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Musculoskeletal finding (finding)\Vertebral column finding (finding)\Finding of vertebra (finding)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Musculoskeletal finding (finding)\Bone finding\Finding of vertebra (finding)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of vertebral column (disorder)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of embryonic structure (disorder)\Congenital ectodermal defect\Neural tube defect\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital malformation syndrome\Malformation sequence\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital ectodermal defect\Neural tube defect\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Neural tube defect\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Congenital anomaly of nervous system\Neural tube defect\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Congenital anomaly of nervous system\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of body system\Disease of nervous system (disorder)\Disorder of the central nervous system (disorder)\Spinal cord disorder (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of vertebral column (disorder)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of back\Disorder of spinal region (disorder)\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of back\Disorder of spinal region (disorder)\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of back\Disorder of spinal region (disorder)\Disorder of vertebral column (disorder)\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of back\Disorder of spinal region (disorder)\Spinal cord disorder (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of back\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Disorder of back\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Disorder of bone development\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital malformation syndrome\Malformation sequence\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of back\Congenital anomaly of vertebral region of back (disorder)\Congenital anomaly of spine\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital ectodermal defect\Neural tube defect\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of nervous system\Neural tube defect\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of nervous system\Congenital anomaly of central nervous system (disorder)\Congenital anomaly of spinal cord\Abnormality of canalization and retrogressive differentiation (disorder)\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of musculoskeletal system\Congenital anomaly of skeletal bone\Spina bifida\A neural tube defect with characteristics of improper closure of the spinal column during embryonal development. In the case of spina bifida occulta the site of the lesion is not exposed, there is a midline defect of the vertebral bodies without protrusion of the spinal cord or meninges.\Occult spinal dysraphism sequence\Split spinal cord malformation (disorder)\Split spinal cord malformation type I

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
5399274018	A rare subtype of split cord malformation characterized by each hemicord contained in its own dural sac, typically with an intervening bony septum.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399275017	A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
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
5399274018	A rare subtype of split cord malformation characterized by each hemicord contained in its own dural sac, typically with an intervening bony septum.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5399275017	A rare subtype of split cord malformation characterised by each hemicord contained in its own dural sac, typically with an intervening bony septum.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3443061001000114	Split-Cord-Malformation Typ I	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3443061001000114	Split-Cord-Malformation Typ I	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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