loading...| Preferred Name |
Congenital micrognathism |
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| Synonyms |
Congenital hypoplasia of mandible Mandibular micrognathism |
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| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/32958008 |
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| Active |
1 |
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| altLabel |
Congenital hypoplasia of mandible Congenital mandibular hypoplasia Congenital small mandible Micrognathism Small jaw Micrognathia Congenital micrognathism (disorder) Congenital micrognathia Micromandible Mandibular micrognathia Mandibular micrognathism |
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| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 |
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| CTV3ID |
X20Rq |
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| cui |
C0025990 |
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| DEFINITION STATUS ID |
900000000000073002 |
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| Effective time |
20140731 |
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| Has associated morphology | ||
| Has finding site | ||
| Has pathological process | ||
| notation |
32958008 |
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| Occurs in | ||
| prefLabel |
Congenital micrognathism |
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| Subset member |
6011000124106~MAPTARGET~Q55.8 6011000124106~MAPTARGET~Q73.8 6011000124106~MAPADVICE~IF CEREBRO-COSTO-MANDIBULAR SYNDROME CHOOSE M26.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 722429003 | Distal limb deficiency with micrognathia syndrome (disorder) | 6011000124106~MAPTARGET~M26.09 6011000124106~MAPADVICE~ALWAYS M26.09 6011000124106~MAPRULE~IFA 109524009 | Congenital vertical mandibular hypoplasia | 6011000124106~MAPADVICE~IF SPLENOGONADAL FUSION, LIMB DEFECT, MICROGNATHIA SYNDROME CHOOSE Q74.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~7 6011000124106~MAPPRIORITY~4 6011000124106~MAPTARGET~Q89.09 6011000124106~MAPRULE~IFA 726724005 | Splenogonadal fusion, limb defect, micrognathia syndrome | AND IFA 248152002 | Female (finding) | 6011000124106~MAPADVICE~ALWAYS M26.09 | DESCENDANTS NOT EXHAUSTIVELY MAPPED 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~MAPRULE~IFA 726724005 | Splenogonadal fusion, limb defect, micrognathia syndrome | AND IFA 248153007 | Male (finding) | 6011000124106~MAPRULE~IFA 722283003 | Agnathia, holoprosencephaly, situs inversus syndrome | 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPADVICE~IF SPLENOGONADAL FUSION, LIMB DEFECT, MICROGNATHIA SYNDROME AND IF MALE CHOOSE Q55.8 | MAP IS CONTEXT DEPENDENT FOR GENDER 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPTARGET~M26.04 6011000124106~MAPTARGET~Q52.8 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 900000000000508004~ACCEPTABILITYID~900000000000549004 6011000124106~MAPADVICE~IF AGENESIS OF CORPUS CALLOSUM, INTELLECTUAL DISABILITY, COLOBOMA, MICROGNATHIA SYNDROME CHOOSE Q04.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF SPLENOGONADAL FUSION, LIMB DEFECT, MICROGNATHIA SYNDROME AND IF FEMALE CHOOSE Q52.8 | MAP IS CONTEXT DEPENDENT FOR GENDER 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~MAPRULE~IFA 51780007 | Cerebro-costo-mandibular syndrome (disorder) | 6011000124106~MAPRULE~IFA 109523003 | Congenital horizontal mandibular hypoplasia | 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 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 6011000124106~MAPADVICE~IF SPLENOGONADAL FUSION, LIMB DEFECT, MICROGNATHIA SYNDROME CHOOSE M26.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPTARGET~K07.0 6011000124106~MAPCATEGORYID~447637006 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) | 6011000124106~MAPRULE~IFA 726724005 | Splenogonadal fusion, limb defect, micrognathia syndrome | 900000000000497000~MAPTARGET~X20Rq 6011000124106~MAPTARGET~Q74.9 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 109525005 | Congenital transverse mandibular hypoplasia (disorder) | 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 6011000124106~MAPTARGET~Q04.9 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~IFA 51780007 | Cerebro-costo-mandibular syndrome | 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~MAPRULE~IFA 109525005 | Congenital transverse mandibular hypoplasia | 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 6011000124106~MAPTARGET~Q04.2 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 6011000124106~MAPRULE~IFA 722429003 | Distal limb deficiency with micrognathia syndrome | 6011000124106~MAPRULE~TRUE 6011000124106~MAPGROUP~3 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPPRIORITY~2 6011000124106~MAPRULE~IFA 722476007 | Thickened earlobe with conductive deafness syndrome | 6011000124106~MAPADVICE~IF SPLENOGONADAL FUSION, LIMB DEFECT, MICROGNATHIA SYNDROME CHOOSE Q89.09 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF CONGENITAL TRANSVERSE MANDIBULAR HYPOPLASIA CHOOSE M26.04 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 722282008 | Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome | |
|
| tui |
T019 |
|
| Type ID |
900000000000003001 900000000000013009 |
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| subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/444897001 |