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Metadata
ID DOID:0080575
Name Larsen-like syndrome B3GAT3 type
Definition A syndrome that is characterized by 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 and has_material_basis_in homozygous mutation in the B3GAT3 gene on chromosome 11q12.
https://www.ncbi.nlm.nih.gov/articles/PMC4654953/, https://www.ncbi.nlm.nih.gov/pubmed/25893793
Xrefs

MIM:245600

ORDO:284139

Subsets

DO_rare_slim

Synonyms

Larsen-like syndrome, B3GAT3 type [EXACT]

multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome [EXACT]

Parent Relationships

is_a syndrome

is_a autosomal recessive disease

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