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770655004: Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3701882017 Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701883010 Microcephalus, brain defect, spasticity, hypernatraemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701884016 Franek Bocker Kahlen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701885015 Microcephalus, brain defect, spasticity, hypernatremia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404858017 Microcephaly-brain defect-spasticity-hypernatremia syndrome is a rare congenital genetic syndrome with a central nervous system malformation as a major feature characterized by microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatremia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. There have been no further descriptions in the literature since 1986. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404859013 Microcephaly-brain defect-spasticity-hypernatraemia syndrome is a rare congenital genetic syndrome with a central nervous system malformation as a major feature characterised by microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatraemia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. There have been no further descriptions in the literature since 1986. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701882017 Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701883010 Microcephalus, brain defect, spasticity, hypernatraemia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701884016 Franek Bocker Kahlen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701885015 Microcephalus, brain defect, spasticity, hypernatremia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3701880013 A rare congenital genetic syndrome with a central nervous system malformation as a major feature. The disorder has characteristics of microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatremia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. Only one familial case with three affected siblings is reported and there have been no further descriptions in the literature since 1986. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3701881012 A rare congenital genetic syndrome with a central nervous system malformation as a major feature. The disorder has characteristics of microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatraemia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. Only one familial case with three affected siblings is reported and there have been no further descriptions in the literature since 1986. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404858017 Microcephaly-brain defect-spasticity-hypernatremia syndrome is a rare congenital genetic syndrome with a central nervous system malformation as a major feature characterized by microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatremia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. There have been no further descriptions in the literature since 1986. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404859013 Microcephaly-brain defect-spasticity-hypernatraemia syndrome is a rare congenital genetic syndrome with a central nervous system malformation as a major feature characterised by microcephaly, hypertonia, developmental delay and cognitive impairment, swallowing difficulty, hypernatraemia, and hypoplasia of the frontal parts and fusion of the lateral ventricles on brain MRI. There have been no further descriptions in the literature since 1986. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3392991001000114 Mikrozephalie-Hirndefekt-Spastik-Hypernatriämie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3392991001000114 Mikrozephalie-Hirndefekt-Spastik-Hypernatriämie-Syndrom 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
Microcephalus, brain defect, spasticity, hypernatremia syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a Disorder of skeletal muscle true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a Spasticity true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a microcéphalie false Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus, brain defect, spasticity, hypernatremia syndrome Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus, brain defect, spasticity, hypernatremia syndrome Interprets Muscle tone true Inferred relationship Existential restriction modifier (core metadata concept) 3
Microcephalus, brain defect, spasticity, hypernatremia syndrome Has interpretation Increased true Inferred relationship Existential restriction modifier (core metadata concept) 3
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a Hypernatraemia true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus, brain defect, spasticity, hypernatremia syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus, brain defect, spasticity, hypernatremia syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 4
Microcephalus, brain defect, spasticity, hypernatremia syndrome Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus, brain defect, spasticity, hypernatremia syndrome Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 5
Microcephalus, brain defect, spasticity, hypernatremia syndrome Interprets Birth head circumference true Inferred relationship Existential restriction modifier (core metadata concept) 4
Microcephalus, brain defect, spasticity, hypernatremia syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Microcephalus, brain defect, spasticity, hypernatremia syndrome Finding site Head structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a Congenital hypoplasia of brain true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Is a Congenital microcephaly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Microcephalus, brain defect, spasticity, hypernatremia syndrome Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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