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 |
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Has finding site | ||
Has interpretation | ||
interprets | ||
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 |