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SNOMED CT, US Edition
| Id | http://purl.bioontology.org/ontology/SNOMEDCT/720408003
http://purl.bioontology.org/ontology/SNOMEDCT/720408003
|
|---|---|
| Preferred Name | Acrofrontofacionasal dysostosis |
| Definitions |
A very rare congenital malformation syndrome with the association of facial and skeletal anomalies, severe intellectual deficit and occasional genitourinary anomalies. The cranio-facial malformations are numerous and variable and include brachycephaly or microbrachycephaly. Other skeletal malformations are also present, with syndactyly of fingers, hypoplastic toes, anomalies of feet structure and fibular hypoplasia. Short stature may be observed. Eye anomalies include bilateral ptosis, cataract and congenital glaucoma. In some male patients, hypospadias and bifid scrotum are reported. Patients suffer from potentially severe intellectual deficit and present with anomalies of the cortical gyration.
A rare congenital malformation syndrome characterized by the association of facial and skeletal anomalies with severe intellectual deficit and occasional genitourinary anomalies.
A rare congenital malformation syndrome characterised by the association of facial and skeletal anomalies with severe intellectual deficit and occasional genitourinary anomalies.
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| Synonyms |
Richieri Costa Colletto syndrome
Acrofrontofacionasal dysostosis (disorder)
Acro-fronto-facio-nasal dysostosis
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A very rare congenital malformation syndrome with the association of facial and skeletal anomalies, severe intellectual deficit and occasional genitourinary anomalies. The cranio-facial malformations are numerous and variable and include brachycephaly or microbrachycephaly. Other skeletal malformations are also present, with syndactyly of fingers, hypoplastic toes, anomalies of feet structure and fibular hypoplasia. Short stature may be observed. Eye anomalies include bilateral ptosis, cataract and congenital glaucoma. In some male patients, hypospadias and bifid scrotum are reported. Patients suffer from potentially severe intellectual deficit and present with anomalies of the cortical gyration. A rare congenital malformation syndrome characterized by the association of facial and skeletal anomalies with severe intellectual deficit and occasional genitourinary anomalies. A rare congenital malformation syndrome characterised by the association of facial and skeletal anomalies with severe intellectual deficit and occasional genitourinary anomalies. |
|---|---|
| prefLabel | Acrofrontofacionasal dysostosis
|
| altLabel |
Richieri Costa Colletto syndrome
Acrofrontofacionasal dysostosis (disorder)
Acro-fronto-facio-nasal dysostosis
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| Type ID |
900000000000003001
900000000000013009
|
| Semantic type UMLS property | |
| Has finding site | |
| Effective time | 20170131
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| cui | C1860118
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| Has pathological process | |
| CTV3ID | XUuAX
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| DEFINITION STATUS ID | 900000000000074008
|
| CASE SIGNIFICANCE ID |
900000000000448009
900000000000017005
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| Occurs in | |
| tui | T047
|
| Active | 1
|
| Has associated morphology | |
| notation | 720408003
|
| type | |
| subClassOf |
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| Subset member | 6011000124106~MAPRULE~IFA 721835008 | Acrofrontofacionasal dysostosis type 2 |
6011000124106~MAPADVICE~IF ACROFRONTOFACIONASAL DYSOSTOSIS TYPE 2 CHOOSE Q87.2 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~ALWAYS Q75.1
447562003~MAPRULE~TRUE
447562003~MAPADVICE~ALWAYS Q75.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
447562003~MAPTARGET~Q75.1
6011000124106~MAPTARGET~Q75.1
6011000124106~MAPRULE~IFA 721835008 | Acrofrontofacionasal dysostosis type 2 (disorder) |
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
900000000000508004~ACCEPTABILITYID~900000000000549004
900000000000497000~MAPTARGET~XUuAX
6011000124106~MAPTARGET~Q87.2
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF ACROFRONTOFACIONASAL DYSOSTOSIS TYPE 2 CHOOSE Q75.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~ALWAYS Q74.8
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPTARGET~Q74.8
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
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