SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Microtia

Synonyms

Congenital small ears

Microtia (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/35045004

Active

1

altLabel

Congenital small ears

Microtia (disorder)

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

P422.

cui

C0152423

DEFINITION STATUS ID

900000000000073002

Effective time

20170131

Focus of

http://purl.bioontology.org/ontology/SNOMEDCT/736012000

http://purl.bioontology.org/ontology/SNOMEDCT/736430001

http://purl.bioontology.org/ontology/SNOMEDCT/736846000

http://purl.bioontology.org/ontology/SNOMEDCT/736100002

http://purl.bioontology.org/ontology/SNOMEDCT/762058009

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/41086002

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/28347008

Has pathological process

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

INACTIVATION INDICATOR

900000000000494007

notation

35045004

Occurs in

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

prefLabel

Microtia

Subset member

6011000124106~MAPADVICE~IF MICROTIA, EYE COLOBOMA, IMPERFORATION OF NASOLACRIMAL DUCT SYNDROME CHOOSE Q17.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~Q17.2

6011000124106~MAPRULE~IFA 721836009 | Hypertelorism with microtia and facial clefting syndrome |

6011000124106~MAPRULE~IFA 732248005 | Coxoauricular syndrome |

900000000000497000~MAPTARGET~P422.

6011000124106~MAPADVICE~IF MICROPHTHALMIA, MICROTIA, FETAL AKINESIA SYNDROME CHOOSE Q17.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF BILATERAL MICROTIA WITH DEAFNESS AND CLEFT PALATE SYNDROME CHOOSE H91.90 | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~ALWAYS Q17.2

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF CONGENITAL DEAFNESS WITH LABYRINTHINE APLASIA, MICROTIA AND MICRODONTIA CHOOSE Q16.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~7

6011000124106~MAPPRIORITY~4

6011000124106~MAPTARGET~Q35.9

6011000124106~MAPADVICE~IF THICKENED EARLOBE WITH CONDUCTIVE DEAFNESS SYNDROME CHOOSE H90.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

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

900000000000490003~VALUEID~900000000000494007

6011000124106~MAPTARGET~Q87.0

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPADVICE~IF MICROPHTHALMIA, MICROTIA, FETAL AKINESIA SYNDROME CHOOSE Q11.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPTARGET~Q87.1

6011000124106~MAPTARGET~Q17.8

6011000124106~MAPADVICE~IF MICROTIA, EYE COLOBOMA, IMPERFORATION OF NASOLACRIMAL DUCT SYNDROME CHOOSE Q13.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~8

6011000124106~MAPADVICE~IF MICROTIA, EYE COLOBOMA, IMPERFORATION OF NASOLACRIMAL DUCT SYNDROME CHOOSE Q10.6 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPTARGET~Q87.19

447562003~MAPGROUP~1

6011000124106~MAPTARGET~Q13.0

6011000124106~MAPTARGET~K00.2

6011000124106~MAPADVICE~IF THICKENED EARLOBE WITH CONDUCTIVE DEAFNESS SYNDROME CHOOSE Q17.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF BILATERAL MICROTIA WITH DEAFNESS AND CLEFT PALATE SYNDROME CHOOSE Q17.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CONGENITAL DEAFNESS WITH LABYRINTHINE APLASIA, MICROTIA AND MICRODONTIA CHOOSE Q17.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 717909004 | Bilateral microtia with deafness and cleft palate syndrome (disorder) |

6011000124106~MAPADVICE~IF HYPERTELORISM WITH MICROTIA AND FACIAL CLEFTING SYNDROME CHOOSE Q18.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 1230344000 | Microphthalmia, microtia, fetal akinesia syndrome |

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~IF COXOAURICULAR SYNDROME CHOOSE Q87.19 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF HYPERTELORISM WITH MICROTIA AND FACIAL CLEFTING SYNDROME CHOOSE Q17.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF ISOTRETINOIN-LIKE SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 717909004 | Bilateral microtia with deafness and cleft palate syndrome |

6011000124106~MAPRULE~IFA 722006004 | Isotretinoin-like syndrome |

6011000124106~MAPRULE~IFA 721836009 | Hypertelorism with microtia and facial clefting syndrome (disorder) |

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF MICROPHTHALMIA, MICROTIA, FETAL AKINESIA SYNDROME CHOOSE R29.898 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q75.2

6011000124106~MAPTARGET~H90.2

6011000124106~MAPTARGET~H91.90

6011000124106~MAPRULE~IFA 722006004 | Isotretinoin embryopathy-like syndrome (disorder) |

6011000124106~MAPTARGET~R29.898

447562003~MAPPRIORITY~1

6011000124106~MAPADVICE~IF CONGENITAL DEAFNESS WITH LABYRINTHINE APLASIA, MICROTIA AND MICRODONTIA CHOOSE K00.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPCATEGORYID~447637006

6011000124106~MAPTARGET~Q17.2

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPTARGET~Q16.5

6011000124106~MAPPRIORITY~5

6011000124106~MAPTARGET~Q10.6

6011000124106~MAPPRIORITY~9

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~IF COXOAURICULAR SYNDROME CHOOSE Q87.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF BILATERAL MICROTIA WITH DEAFNESS AND CLEFT PALATE SYNDROME CHOOSE Q35.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~ALWAYS Q17.2

6011000124106~MAPADVICE~IF ISOTRETINOIN EMBRYOPATHY-LIKE SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~MAPRULE~IFA 722476007 | Thickened earlobe with conductive deafness syndrome (disorder) |

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 702360007 | Congenital deafness with labyrinthine aplasia, microtia and microdontia |

6011000124106~MAPTARGET~Q11.2

6011000124106~MAPGROUP~3

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPRULE~IFA 724139004 | Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome |

6011000124106~MAPPRIORITY~2

6011000124106~MAPRULE~IFA 722476007 | Thickened earlobe with conductive deafness syndrome |

6011000124106~MAPADVICE~IF BILATERAL MICROTIA WITH DEAFNESS AND CLEFT PALATE SYNDROME CHOOSE H91.90 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | CONSIDER LATERALITY SPECIFICATION | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q18.8

6011000124106~MAPADVICE~IF HYPERTELORISM WITH MICROTIA AND FACIAL CLEFTING SYNDROME CHOOSE Q75.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

tui

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/282038006

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MSHFRE/D065817 MSHFRE CUI
http://purl.bioontology.org/ontology/OMIM/MTHU022468 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU000506 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU012400 OMIM CUI
http://purl.bioontology.org/ontology/MDRFRE/10027555 MDRFRE CUI
http://purl.bioontology.org/ontology/OMIM/MTHU013262 OMIM CUI
http://purl.bioontology.org/ontology/SCTSPA/35045004 SCTSPA CUI
http://purl.bioontology.org/ontology/WHOFRE/0683 WHOFRE CUI
http://purl.bioontology.org/ontology/ICD9CM/744.23 ICD9CM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU004157 OMIM CUI
http://purl.bioontology.org/ontology/MDRGER/10027555 MDRGER CUI
http://purl.bioontology.org/ontology/WHO/0683 WHO-ART CUI
http://purl.bioontology.org/ontology/LNC/LA9231-7 LOINC CUI
http://purl.bioontology.org/ontology/ICD10CM/Q17.2 ICD10CM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU030422 OMIM CUI
http://purl.bioontology.org/ontology/MEDDRA/10027555 MEDDRA CUI
http://purl.bioontology.org/ontology/SNMI/D4-B0063 SNMI CUI
http://purl.bioontology.org/ontology/ICD10/Q17.2 ICD10 CUI
http://purl.bioontology.org/ontology/OMIM/MTHU052281 OMIM CUI
http://purl.bioontology.org/ontology/RCD/P422. RCD CUI
http://purl.bioontology.org/ontology/MESH/D065817 MESH CUI
http://purl.obolibrary.org/obo/HP_0008551 HP LOOM
http://purl.obolibrary.org/obo/HP_0008551 HP LOOM
http://purl.obolibrary.org/obo/MONDO_0010920 EFO LOOM
http://purl.obolibrary.org/obo/HP_0008551 OBA LOOM
http://purl.obolibrary.org/obo/MONDO_0010920 MONDO LOOM
http://purl.bioontology.org/ontology/NCBITAXON/311122 NCBITAXON LOOM
http://purl.jp/bio/4/id/200906087805895327 IOBC LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU012400 OMIM LOOM
http://purl.obolibrary.org/obo/HP_0008551 UPHENO LOOM
http://purl.obolibrary.org/obo/HP_0008551 MAXO LOOM
http://purl.bioontology.org/ontology/ICD9CM/744.23 ICD9CM LOOM
http://www.phoc.org.cn/pmo/class/PMO_00006044 PMAPP-PMO LOOM
http://purl.obolibrary.org/obo/MONDO_0010920 DOVES LOOM
http://id.nlm.nih.gov/mesh/D065817 MDM LOOM
http://www.orpha.net/ORDO/Orphanet_83463 ORDO LOOM
http://purl.bioontology.org/ontology/LNC/LA9231-7 LOINC LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q17.2 ICD10CM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0152423 OCHV LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:0420 IFAR LOOM
http://www.gamuts.net/entity#microtia GAMUTS LOOM
http://www.limics.org/hrdo/rdfns#pat_id_11575 HRDO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10027555 MEDDRA LOOM
http://purl.bioontology.org/ontology/SNMI/D4-B0063 SNMI LOOM
http://purl.bioontology.org/ontology/ICD10/Q17.2 ICD10 LOOM
http://purl.bioontology.org/ontology/RCD/P422. RCD LOOM