SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Hypoplasia of mandibular bone

Synonyms

Hypoplasia of mandibular bone (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/444897001

Active

1

altLabel

Hypoplasia of mandibular bone (disorder)

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

XUjqL

cui

C2919331

DEFINITION STATUS ID

900000000000073002

Effective time

20100731

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/55199003

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/91609006

notation

444897001

prefLabel

Hypoplasia of mandibular bone

Subset member

6011000124106~MAPRULE~IFA 32958008 | Congenital micrognathism (disorder) |

6011000124106~MAPTARGET~Q73.8

6011000124106~MAPADVICE~IF CEREBRO-COSTO-MANDIBULAR SYNDROME CHOOSE M26.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPRULE~TRUE

447562003~MAPADVICE~IF CONGENITAL HORIZONTAL MANDIBULAR HYPOPLASIA CHOOSE K07.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 722429003 | Distal limb deficiency with micrognathia syndrome (disorder) |

6011000124106~MAPTARGET~M26.09

447562003~MAPRULE~IFA 109722005 | Condylar hypoplasia with mandibular asymmetry (disorder) |

6011000124106~MAPPRIORITY~7

6011000124106~MAPPRIORITY~4

447562003~MAPTARGET~K10.8

447562003~MAPRULE~IFA 109684004 | Mandibular alveolar hypoplasia (disorder) |

447562003~MAPADVICE~IF CONGENITAL TRANSVERSE MANDIBULAR HYPOPLASIA CHOOSE K07.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

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

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPTARGET~M26.04

6011000124106~MAPTARGET~Q17.8

6011000124106~MAPPRIORITY~8

6011000124106~MAPADVICE~IF DISTAL LIMB DEFICIENCY WITH MICROGNATHIA SYNDROME CHOOSE M26.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF AGNATHIA, HOLOPROSENCEPHALY, SITUS INVERSUS SYNDROME CHOOSE Q89.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF AGENESIS OF CORPUS CALLOSUM, INTELLECTUAL DISABILITY, COLOBOMA, MICROGNATHIA SYNDROME CHOOSE Q04.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPGROUP~1

6011000124106~MAPTARGET~F79

6011000124106~MAPRULE~IFA 109524009 | Congenital vertical mandibular hypoplasia (disorder) |

6011000124106~MAPRULE~IFA 722282008 | Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome (disorder) |

6011000124106~MAPTARGET~Q13.0

6011000124106~MAPADVICE~ALWAYS M26.04

6011000124106~MAPRULE~IFA 51780007 | Cerebro-costo-mandibular syndrome (disorder) |

6011000124106~MAPADVICE~IF CEREBRO-COSTO-MANDIBULAR SYNDROME CHOOSE Q76.6 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

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

447562003~CORRELATIONID~447561005

447562003~MAPRULE~OTHERWISE TRUE

6011000124106~MAPTARGET~Q04.0

6011000124106~MAPADVICE~IF AGENESIS OF CORPUS CALLOSUM, INTELLECTUAL DISABILITY, COLOBOMA, MICROGNATHIA SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~K07.0

6011000124106~MAPCATEGORYID~447637006

900000000000497000~MAPTARGET~XUjqL

6011000124106~MAPTARGET~Q89.3

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF CONGENITAL HORIZONTAL MANDIBULAR HYPOPLASIA CHOOSE M26.04 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 722283003 | Agnathia, holoprosencephaly, situs inversus syndrome (disorder) |

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPRULE~IFA 109525005 | Congenital transverse mandibular hypoplasia (disorder) |

447562003~MAPTARGET~

6011000124106~MAPTARGET~H90.2

6011000124106~MAPRULE~IFA 109523003 | Congenital horizontal mandibular hypoplasia (disorder) |

6011000124106~MAPADVICE~IF CONGENITAL VERTICAL MANDIBULAR HYPOPLASIA CHOOSE M26.04 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

6011000124106~MAPTARGET~Q76.6

447562003~MAPADVICE~SOURCE SNOMED CONCEPT IS AMBIGUOUS

6011000124106~MAPTARGET~Q04.9

447562003~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~ALWAYS M26.04 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

6011000124106~MAPADVICE~IF CEREBRO-COSTO-MANDIBULAR SYNDROME CHOOSE Q04.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPGROUP~4

6011000124106~MAPADVICE~IF DISTAL LIMB DEFICIENCY WITH MICROGNATHIA SYNDROME CHOOSE Q73.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~9

6011000124106~MAPADVICE~IF AGNATHIA, HOLOPROSENCEPHALY, SITUS INVERSUS SYNDROME CHOOSE Q04.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPCATEGORYID~447639009

447562003~MAPADVICE~IF CONDYLAR HYPOPLASIA WITH MANDIBULAR ASYMMETRY CHOOSE K10.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q04.2

447562003~MAPPRIORITY~3

447562003~MAPRULE~IFA 109524009 | Congenital vertical mandibular hypoplasia (disorder) |

447562003~MAPRULE~IFA 109525005 | Congenital transverse mandibular hypoplasia (disorder) |

447562003~MAPCATEGORYID~447639009

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

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

6011000124106~CORRELATIONID~447561005

6011000124106~MAPADVICE~IF AGENESIS OF CORPUS CALLOSUM, INTELLECTUAL DISABILITY, COLOBOMA, MICROGNATHIA SYNDROME CHOOSE M26.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF AGENESIS OF CORPUS CALLOSUM, INTELLECTUAL DISABILITY, COLOBOMA, MICROGNATHIA SYNDROME CHOOSE Q13.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~ALWAYS K07.0

447562003~MAPCATEGORYID~447640006

447562003~MAPPRIORITY~2

447562003~MAPRULE~IFA 109523003 | Congenital horizontal mandibular hypoplasia (disorder) |

6011000124106~MAPRULE~TRUE

6011000124106~MAPGROUP~3

6011000124106~MAPPRIORITY~3

6011000124106~MAPPRIORITY~2

6011000124106~MAPADVICE~IF CONGENITAL MICROGNATHISM CHOOSE M26.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CONGENITAL TRANSVERSE MANDIBULAR HYPOPLASIA CHOOSE M26.04 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPADVICE~IF CONGENITAL VERTICAL MANDIBULAR HYPOPLASIA CHOOSE K07.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~4

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/235080003

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