Id |
Description |
Lang |
Type |
Status |
Case? |
Module |
Reference Sets |
3643814016 |
Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
GB English: Acceptable (foundation metadata concept) |
3643815015 |
Multiple joint dislocations, short stature, craniofacial dysmorphism, congenital heart defects syndrome |
en |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
SNOMED CT core |
GB English: Acceptable (foundation metadata concept) |
3643816019 |
Larsen-like syndrome B3GAT3 type |
en |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
GB English: Preferred (foundation metadata concept) |
3643817011 |
Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type (disorder) |
en |
Fully specified name |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
GB English: Preferred (foundation metadata concept) |
3643818018 |
A rare genetic primary bone dysplasia with characteristics of laxity, dislocations and contractures of the joints, short stature, foot deformities (e.g. clubfeet), broad tips of fingers and toes, short neck, dysmorphic facial features (hypertelorism, downslanting palpebral fissures, upturned nose with anteverted nares, high arched palate) and various cardiac malformations. Severe disease is associated with multiple fractures, osteopenia, arachnodactyly and blue sclerae. A broad spectrum of additional features, including scoliosis, radio-ulnar synostosis, mild developmental delay and various eye disorders (glaucoma, amblyopia, hyperopia, astigmatism, ptosis), are also reported. |
en |
Definition |
Active |
Entire term case sensitive (core metadata concept) |
SNOMED CT core |
GB English: Preferred (foundation metadata concept) |
2103311000172112 |
"syndrome de Larsen : type bêta-1,3 glucuronyltransférase 3" |
fr |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
Belgian module (core metadata concept) |
Belgian French language reference set (foundation metadata concept): Acceptable (foundation metadata concept) |
2103321000172119 |
"syndrome de dislocations articulaires multiples, petite taille - dysmorphie craniofaciale, anomalies cardiaques congénitales" |
fr |
Synonym (core metadata concept) |
Active |
Entire term case insensitive (core metadata concept) |
Belgian module (core metadata concept) |
Belgian French language reference set (foundation metadata concept): Preferred (foundation metadata concept) |
2103331000172116 |
"syndrome de Larsen-like : type B3GAT3 (beta-1,3 glucuronyltransferase 3)" |
fr |
Synonym (core metadata concept) |
Active |
Only initial character case insensitive (core metadata concept) |
Belgian module (core metadata concept) |
Belgian French language reference set (foundation metadata concept): Acceptable (foundation metadata concept) |
2103291000172113 |
Larsen-achtig syndroom B3GAT3-type |
nl |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
Belgian module (core metadata concept) |
Belgian Dutch language reference set (foundation metadata concept): Acceptable (foundation metadata concept) |
2103301000172114 |
"Larsen-achtig syndroom bèta-1,3-glucuronyltransferase 3-type" |
nl |
Synonym (core metadata concept) |
Active |
Entire term case sensitive (core metadata concept) |
Belgian module (core metadata concept) |
Belgian Dutch language reference set (foundation metadata concept): Preferred (foundation metadata concept) |