SNOMED CT

Last uploaded: January 31, 2024
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Preferred Name

Bilateral optic atrophy of eyes
Synonyms

Optic atrophy of both eyes

Optic atrophy of bilateral eyes (disorder)
ID

http://purl.bioontology.org/ontology/SNOMEDCT/15632891000119109
Active

1
altLabel

Optic atrophy of both eyes

Optic atrophy of bilateral eyes

Optic atrophy of bilateral eyes (disorder)
CASE SIGNIFICANCE ID

900000000000448009
CTV3ID

XV73n
cui

C2013200
DEFINITION STATUS ID

900000000000073002
Effective time

20190131
Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/13331008
Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/724379002

http://purl.bioontology.org/ontology/SNOMEDCT/724380004
notation

15632891000119109
prefLabel

Bilateral optic atrophy of eyes
Subset member

6011000124106~MAPADVICE~IF DIABETES MELLITUS AND INSIPIDUS WITH OPTIC ATROPHY AND DEAFNESS CHOOSE E11.39 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE ISOLATED OPTIC ATROPHY CHOOSE H47.22 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF DIABETES MELLITUS AND INSIPIDUS WITH OPTIC ATROPHY AND DEAFNESS CHOOSE E23.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~7

6011000124106~MAPADVICE~ALWAYS H47.20

6011000124106~MAPPRIORITY~4

447562003~MAPTARGET~H47.2

6011000124106~MAPADVICE~IF WOLFRAM SYNDROME CHOOSE E11.69 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

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

6011000124106~MAPTARGET~H47.20

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPRULE~IFA 349161000119106 | Bilateral partial optic atrophy |

6011000124106~MAPRULE~IFA 1156823006 | Autosomal recessive bilateral optic atrophy |

6011000124106~MAPPRIORITY~8

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

6011000124106~MAPTARGET~E11.39

6011000124106~MAPADVICE~IF HEREDITARY BILATERAL OPTIC ATROPHY CHOOSE H47.22 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF WOLFRAM SYNDROME CHOOSE H91.90 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 15699081000119101 | Hereditary bilateral optic atrophy |

6011000124106~MAPRULE~IFA 70694009 | Diabetes mellitus AND insipidus with optic atrophy AND deafness |

6011000124106~MAPTARGET~H47.213

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF BILATERAL PRIMARY OPTIC ATROPHY CHOOSE H47.213 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~H91.90

6011000124106~MAPADVICE~IF DIABETES MELLITUS AND INSIPIDUS WITH OPTIC ATROPHY AND DEAFNESS CHOOSE H91.90 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE BILATERAL OPTIC ATROPHY CHOOSE H47.22 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPTARGET~E23.2

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPGROUP~4

447562003~MAPADVICE~ALWAYS H47.2

6011000124106~MAPADVICE~IF DIABETES MELLITUS AND INSIPIDUS WITH OPTIC ATROPHY AND DEAFNESS CHOOSE E11.69 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 70694009 | Wolfram syndrome |

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPRULE~IFA 344271000119107 | Bilateral primary optic atrophy |

6011000124106~MAPADVICE~IF WOLFRAM SYNDROME CHOOSE E23.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF BILATERAL PARTIAL OPTIC ATROPHY CHOOSE H47.293 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 1197151003 | Autosomal recessive isolated optic atrophy |

6011000124106~MAPTARGET~E11.69

900000000000497000~MAPTARGET~XV73n

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~CORRELATIONID~447561005

6011000124106~MAPTARGET~H47.22

6011000124106~MAPGROUP~3

6011000124106~MAPTARGET~H47.293

6011000124106~MAPPRIORITY~3

6011000124106~MAPADVICE~IF BILATERAL ATROPHY OF OPTIC NERVES FOLLOWING INFLAMMATION CHOOSE H47.293 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPADVICE~IF WOLFRAM SYNDROME CHOOSE E11.39 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~2

6011000124106~MAPRULE~IFA 680991000119108 | Bilateral atrophy of optic nerves following inflammation |
tui

T033
Type ID

900000000000003001

900000000000013009
subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/15632811000119100

http://purl.bioontology.org/ontology/SNOMEDCT/15731881000119107

http://purl.bioontology.org/ontology/SNOMEDCT/15632851000119104
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