SNOMED CT

Last uploaded: January 31, 2024
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Preferred Name

Congenital oculocutaneous hypopigmentation
Synonyms

Congenital oculocutaneous hypopigmentation (disorder)
ID

http://purl.bioontology.org/ontology/SNOMEDCT/61649007
Active

1
altLabel

Congenital oculocutaneous hypopigmentation (disorder)
CASE SIGNIFICANCE ID

900000000000448009
CTV3ID

XUHcJ
cui

C0265983
DEFINITION STATUS ID

900000000000073002
Effective time

20170131
Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/89031001
Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/39937001

http://purl.bioontology.org/ontology/SNOMEDCT/81745001
Has pathological process

http://purl.bioontology.org/ontology/SNOMEDCT/308490002
notation

61649007
Occurs in

http://purl.bioontology.org/ontology/SNOMEDCT/255399007
prefLabel

Congenital oculocutaneous hypopigmentation
Subset member

447562003~MAPRULE~TRUE

900000000000497000~MAPTARGET~XUHcJ

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

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPRULE~IFA 719824001 | Vici syndrome |

447562003~MAPGROUP~1

6011000124106~MAPTARGET~Q82.8

6011000124106~MAPTARGET~Q87.89

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPRULE~IFA 719824001 | Vici syndrome (disorder) |

6011000124106~MAPRULE~IFA 722113001 | Osteoporosis and oculocutaneous hypopigmentation syndrome |

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~Q82.8

6011000124106~MAPADVICE~IF OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME CHOOSE M81.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPRULE~OTHERWISE TRUE

447562003~MAPADVICE~ALWAYS Q82.8

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPRULE~IFA 722113001 | Osteoporosis and oculocutaneous hypopigmentation syndrome (disorder) |

6011000124106~MAPADVICE~IF OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME CHOOSE Q82.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~ALWAYS Q82.8 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

6011000124106~MAPPRIORITY~1

6011000124106~MAPADVICE~ALWAYS Q82.8

6011000124106~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF VICI SYNDROME CHOOSE Q87.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~TRUE

6011000124106~MAPTARGET~M81.8

6011000124106~MAPPRIORITY~3

6011000124106~MAPPRIORITY~2
tui

T019
Type ID

900000000000003001

900000000000013009
subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/19416009

http://purl.bioontology.org/ontology/SNOMEDCT/1953005

http://purl.bioontology.org/ontology/SNOMEDCT/301905003
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