SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Spastic tetraplegia

Synonyms

Spastic tetraplegia (disorder)

Spastic quadriplegia

ID

http://purl.bioontology.org/ontology/SNOMEDCT/192965001

Active

1

altLabel

Spastic tetraplegia (disorder)

Spastic quadriplegia

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

F2401

cui

C0426970

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/21483005

http://purl.bioontology.org/ontology/SNOMEDCT/66019005

Has interpretation

http://purl.bioontology.org/ontology/SNOMEDCT/2667000

interprets

http://purl.bioontology.org/ontology/SNOMEDCT/363847004

http://purl.bioontology.org/ontology/SNOMEDCT/255324009

notation

192965001

prefLabel

Spastic tetraplegia

Subset member

6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS, INTELLECTUAL DISABILITY, SPASTIC QUADRIPLEGIA SYNDROME CHOOSE F78.A9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS, MICROCEPHALUS, TETRAPLEGIA SYNDROME CHOOSE Q80.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF NKX6-2-RELATED AUTOSOMAL RECESSIVE HYPOMYELINATING LEUKODYSTROPHY CHOOSE E75.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~ALWAYS G80.0

6011000124106~MAPTARGET~F78.A9

6011000124106~MAPPRIORITY~4

6011000124106~MAPRULE~IFA 1217379007 | NKX6-2-related autosomal recessive hypomyelinating leukodystrophy |

6011000124106~MAPRULE~IFA 1197059004 | Congenital ichthyosis, microcephalus, tetraplegia syndrome |

6011000124106~MAPADVICE~IF SPASTIC TETRAPLEGIA, RETINITIS PIGMENTOSA, INTELLECTUAL DISABILITY SYNDROME CHOOSE H35.52 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 782887003 | Inherited congenital spastic tetraplegia |

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS, MICROCEPHALUS, TETRAPLEGIA SYNDROME CHOOSE Q02 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPTARGET~G82.50

447562003~MAPGROUP~1

6011000124106~MAPTARGET~F79

447562003~MAPADVICE~ALWAYS G82.4

6011000124106~MAPADVICE~ALWAYS G82.50

447562003~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS, INTELLECTUAL DISABILITY, SPASTIC QUADRIPLEGIA SYNDROME CHOOSE Q80.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q80.9

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPTARGET~G80.0

900000000000509007~ACCEPTABILITYID~900000000000548007

900000000000497000~MAPTARGET~F2401

6011000124106~MAPTARGET~H35.52

6011000124106~MAPADVICE~IF SPASTIC TETRAPLEGIA, RETINITIS PIGMENTOSA, INTELLECTUAL DISABILITY SYNDROME CHOOSE F78.A9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS, MICROCEPHALUS, TETRAPLEGIA SYNDROME CHOOSE G80.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF INHERITED CONGENITAL SPASTIC TETRAPLEGIA CHOOSE G80.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~IF CONGENITAL ICHTHYOSIS, INTELLECTUAL DISABILITY, SPASTIC QUADRIPLEGIA SYNDROME CHOOSE G80.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF SPASTIC TETRAPLEGIA, RETINITIS PIGMENTOSA, INTELLECTUAL DISABILITY SYNDROME CHOOSE G80.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF SPASTIC TETRAPLEGIA, RETINITIS PIGMENTOSA, INTELLECTUAL DISABILITY SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

447562003~MAPTARGET~G82.4

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 723621000 | Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome |

6011000124106~MAPTARGET~Q02

6011000124106~MAPRULE~TRUE

6011000124106~MAPRULE~IFA 1208936008 | Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome |

6011000124106~MAPGROUP~3

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

6011000124106~MAPTARGET~E75.29

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/128605003

http://purl.bioontology.org/ontology/SNOMEDCT/386781001

http://purl.bioontology.org/ontology/SNOMEDCT/11538006

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