SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Oculomotor apraxia
Synonyms

Oculomotor apraxia (disorder)

Oculomotor dyspraxia

ID

http://purl.bioontology.org/ontology/SNOMEDCT/193662007

Active

1

altLabel

Oculomotor apraxia (disorder)

Oculomotor dyspraxia

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

F4835

cui

C3489733

DEFINITION STATUS ID

900000000000074008

Effective time

20040131

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/49549006

INACTIVATION INDICATOR

900000000000482003

900000000000495008

notation

193662007

prefLabel

Oculomotor apraxia

Subset member

447562003~MAPADVICE~ALWAYS H51.8 | MAPPED FOLLOWING WHO GUIDANCE

6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA WITH OCULOMOTOR APRAXIA TYPE 2 CHOOSE H51.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF PSYCHOMOTOR REGRESSION, OCULOMOTOR APRAXIA, MOVEMENT DISORDER, NEPHROPATHY SYNDROME CHOOSE N07.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~ALWAYS H51.8

6011000124106~MAPTARGET~N07.9

6011000124106~MAPTARGET~F78.A9

6011000124106~MAPPRIORITY~4

6011000124106~MAPTARGET~H51.8

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

6011000124106~MAPTARGET~R48.3

6011000124106~MAPADVICE~IF BALINT SYNDROME CHOOSE R48.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPTARGET~G25.9

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

900000000000527005~TARGETCOMPONENT~26018001

6011000124106~MAPADVICE~IF BALINT SYNDROME CHOOSE H51.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 20485009 | Cortical paralysis of fixation syndrome (disorder) |

6011000124106~MAPTARGET~G11.9

6011000124106~MAPRULE~IFA 20485009 | Cortical paralysis of fixation syndrome |

6011000124106~MAPADVICE~IF CEREBELLAR ATAXIA, INTELLECTUAL DISABILITY, OCULOMOTOR APRAXIA, CEREBELLAR CYSTS SYNDROME CHOOSE H51.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 725408001 | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 |

900000000000490003~VALUEID~900000000000495008

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPRULE~IFA 763344007 | Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome |

6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA WITH OCULOMOTOR APRAXIA TYPE 2 CHOOSE G11.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF PSYCHOMOTOR REGRESSION, OCULOMOTOR APRAXIA, MOVEMENT DISORDER, NEPHROPATHY SYNDROME CHOOSE R41.843 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPGROUP~1

6011000124106~MAPTARGET~F79

900000000000489007~VALUEID~900000000000482003

6011000124106~MAPTARGET~Q04.6

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPRULE~IFA 765212008 | Balint syndrome |

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPTARGET~G11.8

447562003~MAPTARGET~H51.8

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF CORTICAL PARALYSIS OF FIXATION SYNDROME CHOOSE H53.16 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 1187043002 | Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome |

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~IF PSYCHOMOTOR REGRESSION, OCULOMOTOR APRAXIA, MOVEMENT DISORDER, NEPHROPATHY SYNDROME CHOOSE H51.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CEREBELLAR ATAXIA, INTELLECTUAL DISABILITY, OCULOMOTOR APRAXIA, CEREBELLAR CYSTS SYNDROME CHOOSE F78.A9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPGROUP~4

6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA WITH OCULOMOTOR APRAXIA TYPE 1 CHOOSE G11.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~IF PSYCHOMOTOR REGRESSION, OCULOMOTOR APRAXIA, MOVEMENT DISORDER, NEPHROPATHY SYNDROME CHOOSE G25.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000497000~MAPTARGET~F4835

6011000124106~MAPADVICE~IF CEREBELLAR ATAXIA, INTELLECTUAL DISABILITY, OCULOMOTOR APRAXIA, CEREBELLAR CYSTS SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF BALINT SYNDROME CHOOSE G98.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE CEREBELLAR ATAXIA WITH OCULOMOTOR APRAXIA TYPE 1 CHOOSE H51.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF CEREBELLAR ATAXIA, INTELLECTUAL DISABILITY, OCULOMOTOR APRAXIA, CEREBELLAR CYSTS SYNDROME CHOOSE G11.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 715366004 | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder) |

6011000124106~MAPRULE~TRUE

6011000124106~MAPGROUP~3

6011000124106~MAPRULE~IFA 715366004 | Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 |

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPTARGET~H53.16

6011000124106~MAPPRIORITY~2

6011000124106~MAPADVICE~ALWAYS H51.8 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

6011000124106~MAPADVICE~IF CEREBELLAR ATAXIA, INTELLECTUAL DISABILITY, OCULOMOTOR APRAXIA, CEREBELLAR CYSTS SYNDROME CHOOSE Q04.6 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~G98.8

6011000124106~MAPTARGET~R41.843

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/22066006

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