SNOMED CT

Last uploaded: January 31, 2024
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Preferred Name

Café au lait spots
Synonyms

Café au lait spot (disorder)

Cafe-au-lait spots
ID

http://purl.bioontology.org/ontology/SNOMEDCT/201281002
Active

1
altLabel

Café au lait spot (disorder)

Cafe au lait spots

Café au lait spot

Cafe-au-lait spots
CASE SIGNIFICANCE ID

900000000000020002

900000000000448009
CTV3ID

M291.
cui

C0221263
DEFINITION STATUS ID

900000000000074008
Effective time

20020131
Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/79644001
Has finding site

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

201281002
prefLabel

Café au lait spots
Subset member

6011000124106~MAPTARGET~Q93.2

6011000124106~MAPTARGET~Q82.9

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE R64 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 403758009 | Café-au-lait spots and ring chromosome 11 |

6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE R63.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 1177178005 | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome |

6011000124106~MAPPRIORITY~4

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

6011000124106~MAPADVICE~IF CAFÉ-AU-LAIT SPOTS AND RING CHROMOSOME 11 CHOOSE Q93.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q87.0

6011000124106~MAPTARGET~

6011000124106~MAPTARGET~P05.9

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPADVICE~IF MCCUNE ALBRIGHT SYNDROME CHOOSE Q78.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE Q82.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF LEGIUS SYNDROME CHOOSE Q85.01 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPTARGET~Q85.01

6011000124106~MAPTARGET~R63.0

447562003~MAPTARGET~L81.3

447562003~MAPGROUP~1

447562003~MAPRULE~IFA 703541007 | Neurofibromatosis type 1-like syndrome (disorder) |

447562003~CORRELATIONID~447561005

447562003~MAPRULE~OTHERWISE TRUE

6011000124106~MAPRULE~IFA 726029005 | McCune Albright syndrome |

900000000000497000~MAPTARGET~M291.

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF FACIAL DYSMORPHISM, ANOREXIA, CACHEXIA, EYE AND SKIN ANOMALIES SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

447562003~MAPADVICE~IF NEUROFIBROMATOSIS TYPE 1-LIKE SYNDROME CHOOSE Q85.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPCATEGORYID~447637006

6011000124106~MAPTARGET~R64

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPGROUP~4

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~ALWAYS L81.3

6011000124106~MAPTARGET~Q78.1

6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, CONGENITAL MULTIPLE CAFÉ AU LAIT MACULES, INCREASED SISTER CHROMATID EXCHANGE SYNDROME CHOOSE P05.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPCATEGORYID~447639009

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, CONGENITAL MULTIPLE CAFÉ AU LAIT MACULES, INCREASED SISTER CHROMATID EXCHANGE SYNDROME CHOOSE L81.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 782949007 | Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome |

6011000124106~MAPTARGET~L81.3

447562003~MAPPRIORITY~2

6011000124106~MAPADVICE~IF INTRAUTERINE GROWTH RESTRICTION, CONGENITAL MULTIPLE CAFÉ AU LAIT MACULES, INCREASED SISTER CHROMATID EXCHANGE SYNDROME CHOOSE Q99.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 703541007 | Legius syndrome |

6011000124106~MAPGROUP~3

447562003~MAPADVICE~ALWAYS L81.3

6011000124106~MAPADVICE~IF NEUROFIBROMATOSIS TYPE 1-LIKE SYNDROME CHOOSE Q85.01 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

447562003~MAPTARGET~Q85.8

6011000124106~MAPRULE~IFA 703541007 | Neurofibromatosis type 1-like syndrome (disorder) |

6011000124106~MAPTARGET~Q99.8
tui

T033
Type ID

900000000000003001

900000000000013009
subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/46690002
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