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763717004: Sporadic fetal brain disruption sequence (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3643466016 Sporadic foetal brain disruption sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643467013 Sporadic fetal brain disruption sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643469011 Sporadic fetal brain disruption sequence (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404157012 Sporadic fetal brain disruption sequence is a rare, non-syndromic, central nervous system malformation disorder characterized by severe microcephaly (average occipitofrontal circumference -5.8 SD), overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404158019 Sporadic fetal brain disruption sequence is a rare, non-syndromic, central nervous system malformation disorder characterised by severe microcephaly (average occipitofrontal circumference -5.8 SD), overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643466016 Sporadic foetal brain disruption sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643467013 Sporadic fetal brain disruption sequence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643469011 Sporadic fetal brain disruption sequence (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643468015 A rare non-syndromic central nervous system malformation disorder with characteristics of severe microcephaly, overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404157012 Sporadic fetal brain disruption sequence is a rare, non-syndromic, central nervous system malformation disorder characterized by severe microcephaly (average occipitofrontal circumference -5.8 SD), overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404158019 Sporadic fetal brain disruption sequence is a rare, non-syndromic, central nervous system malformation disorder characterised by severe microcephaly (average occipitofrontal circumference -5.8 SD), overlapping sutures, keel-like occipital bone prominence, scalp rugae with normal hair pattern and signs of neurological impairment. Brain imaging may show ventriculomegaly, cortical tissue deficit, and hydranencephaly. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3393131001000116 Sporadische Fetal-brain-disruption-Sequenz de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
938141000172114 syndrome de destruction du cerveau foetal sporadique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
938141000172114 syndrome de destruction du cerveau foetal sporadique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3393131001000116 Sporadische Fetal-brain-disruption-Sequenz de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Sporadic fetal brain disruption sequence Is a Fetal microcephaly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic fetal brain disruption sequence Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic fetal brain disruption sequence Occurrence Fetal period (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic fetal brain disruption sequence Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic fetal brain disruption sequence Is a Disorder of brain true Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic fetal brain disruption sequence Is a Malformation of central nervous system of fetus (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Sporadic fetal brain disruption sequence Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic fetal brain disruption sequence Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Sporadic fetal brain disruption sequence Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sporadic fetal brain disruption sequence Interprets Head circumference true Inferred relationship Existential restriction modifier (core metadata concept) 2
Sporadic fetal brain disruption sequence Associated morphology Growth alteration true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sporadic fetal brain disruption sequence Finding site Head structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sporadic fetal brain disruption sequence Occurrence Fetal period (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Sporadic fetal brain disruption sequence Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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