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loading...| Preferred Name |
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| Synonyms |
SCS ACS3 Acrocephalosyndactyly type 3 |
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| Definitions |
Saethre-Chotzen syndrome (SCS) is an inherited craniosynostosis syndrome characterized by unilateral or bilateral coronal synostosis, facial asymmetry, ptosis, strabismus and small ears with prominent crus, among other less common manifestations. |
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| ID |
http://www.orpha.net/ORDO/Orphanet_794 |
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| Obsolete |
true |
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| database_cross_reference |
UMLS:C0175699 OMIM:101400 OMIM:180750 ICD10:Q87.0 |
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| definition |
Saethre-Chotzen syndrome (SCS) is an inherited craniosynostosis syndrome characterized by unilateral or bilateral coronal synostosis, facial asymmetry, ptosis, strabismus and small ears with prominent crus, among other less common manifestations. |
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| definition_citation |
orphanet |
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| deprecated |
true |
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| has_exact_synonym |
Acrocephalosyndactyly type 3 ACS3 SCS |
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| label |
obsolete_Saethre-Chotzen syndrome |
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| obsoleted_in_version |
3.41.0 |
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| reason_for_obsolescence |
Replaced with Mondo term. |
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| term replaced by | ||
| subClassOf |