Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3327896015 | Lowry MacLean syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3327897012 | Lowry MacLean syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402750016 | Lowry-MacLean syndrome is a very rare syndrome characterized by microcephaly, craniosynostosis, glaucoma, growth failure and visceral malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402751017 | Lowry-MacLean syndrome is a very rare syndrome characterised by microcephaly, craniosynostosis, glaucoma, growth failure and visceral malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3327896015 | Lowry MacLean syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3327897012 | Lowry MacLean syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3327898019 | A very rare syndrome with characteristics of microcephaly, craniosynostosis, glaucoma, growth failure and visceral malformations. Only three cases have been reported in the literature in three unrelated families. Dysmorphic features include trigonocephaly, exotropia, cleft palate, beaked nose and low-set ears. All the affected patients have associated congenital visceral malformations including congenital heart defects, diaphragmatic hernia, genital or cerebral abnormalities. The demonstration of congenital glaucoma, hallmark of the syndrome, in the father of an affected patient, supports autosomal dominant inheritance. Prognosis is poor. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402750016 | Lowry-MacLean syndrome is a very rare syndrome characterized by microcephaly, craniosynostosis, glaucoma, growth failure and visceral malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5402751017 | Lowry-MacLean syndrome is a very rare syndrome characterised by microcephaly, craniosynostosis, glaucoma, growth failure and visceral malformations. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3440931001000114 | Lowry-Maclean-Syndrom | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6366911000241119 | syndrome de Lowry-MacLean | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
6366911000241119 | syndrome de Lowry-MacLean | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3440931001000114 | Lowry-Maclean-Syndrom | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)