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SNOMED CT, US Edition
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/SNOMEDCT/89444000
http://purl.bioontology.org/ontology/SNOMEDCT/89444000
|
|---|---|
| Preferred Name | Oromandibular-limb hypogenesis spectrum |
| Definitions |
A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies).
|
| Synonyms |
Facial-limb disruptive spectrum
Hypoglossia-hypodactyly syndrome
Oromandibular-limb hypogenesis spectrum (disorder)
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). |
|---|---|
| altLabel |
Facial-limb disruptive spectrum
Hypoglossia-hypodactyly syndrome
Oromandibular-limb hypogenesis spectrum (disorder)
|
| prefLabel | Oromandibular-limb hypogenesis spectrum
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID |
900000000000020002
900000000000448009
900000000000017005
|
| notation | 89444000
|
| Effective time | 20020131
|
| Active | 1
|
| Has finding site | |
| INACTIVATION INDICATOR | 900000000000494007
|
| Has pathological process | |
| subClassOf | |
| Semantic type UMLS property | |
| type | |
| Subset member | 6011000124106~MAPADVICE~ALWAYS M26.89
447562003~MAPRULE~TRUE
6011000124106~MAPADVICE~ALWAYS Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE
6011000124106~MAPRULE~IFA 717814004 | Glossopalatine ankylosis (disorder) |
6011000124106~MAPRULE~IFA 733034007 | Charlie M syndrome |
6011000124106~MAPTARGET~Q38.8
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
900000000000490003~VALUEID~900000000000494007
6011000124106~MAPTARGET~Q87.0
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
447562003~MAPADVICE~ALWAYS Q87.0
6011000124106~MAPADVICE~IF CHARLIE M SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000497000~MAPTARGET~F3262
900000000000508004~ACCEPTABILITYID~900000000000549004
6011000124106~MAPTARGET~M26.89
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF CHARLIE M SYNDROME CHOOSE Q74.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 717814004 | Glossopalatine ankylosis |
6011000124106~MAPTARGET~Q74.9
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~Q75.2
6011000124106~MAPADVICE~IF CHARLIE M SYNDROME CHOOSE Q75.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~ALWAYS Q74.9
6011000124106~MAPRULE~TRUE
6011000124106~MAPGROUP~3
6011000124106~MAPPRIORITY~3
447562003~MAPTARGET~Q87.0
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
6011000124106~MAPADVICE~IF GLOSSOPALATINE ANKYLOSIS CHOOSE Q38.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
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| DEFINITION STATUS ID | 900000000000074008
|
| tui |
T047
T019
|
| CTV3ID | F3262
|
| Occurs in | |
| cui | C0221060
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| Has associated morphology |
| Delete | Subject | Author | Type | Created |
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| No notes to display |