ZFIN Human Disease: Larsen syndrome

OBO ID: DOID:14764

OBO ID: DOID:14764

Term Name:	Larsen syndrome	Search Ontology:
Synonyms:	dominant larsen syndrome
Definition:	A syndrome that is characterized by autosomal dominant inheritance of large-joint dislocations and characteristic craniofacial abnormalities. (2)
References:	GARD:6860 MESH:C580241 OMIM:150250
Ontology:	Human Disease ( DOID:14764 )

Relationships

is a type of:	autosomal dominant disease syndrome autosomal dominant disease syndrome Show first 5 Terms

OTHER Larsen syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FLNB	flnb	Larsen syndrome	150250

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None