Larsen-like syndrome B3GAT3 type
human disease
Press Enter · cited answer in seconds
0 sources
Summary
Larsen-like syndrome B3GAT3 type is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- Larsen-like syndrome B3GAT3 type's instance of is recorded as developmental defect during embryogenesis[3].
- Larsen-like syndrome B3GAT3 type's instance of is recorded as rare disease[4].
- Larsen-like syndrome B3GAT3 type's instance of is recorded as class of disease[5].
- Larsen-like syndrome B3GAT3 type is a type of primary bone dysplasia with multiple joint dislocations[6].
- Larsen-like syndrome B3GAT3 type is a type of congenital disorder of glycosylation with cardiac malformation as a major feature[7].
- Larsen-like syndrome B3GAT3 type is a type of congenital disorder of glycosylation-related bone disorder[8].
- Larsen-like syndrome B3GAT3 type is a type of disorder of O-xylosylglycan synthesis[9].
- Larsen-like syndrome B3GAT3 type is a type of rare developmental defect with connective tissue involvement[10].
- Larsen-like syndrome B3GAT3 type is a type of autosomal recessive disease[11].
- Larsen-like syndrome B3GAT3 type is a type of syndrome[12].
- Larsen-like syndrome B3GAT3 type's genetic association is recorded as B3GAT3[13].
- Larsen-like syndrome B3GAT3 type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_284139[14].
- Larsen-like syndrome B3GAT3 type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080575[15].
- Larsen-like syndrome B3GAT3 type's exact match is recorded as http://identifiers.org/doid/DOID:0080575[16].
- Larsen-like syndrome B3GAT3 type's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Larsen-like syndrome B3GAT3 type is known by 7 alternative names across languages and contexts.[2]