ZFIN Human Disease: multiple synostoses syndrome

OBO ID: DOID:0050794

Term Name:	multiple synostoses syndrome		Search Ontology:
Synonyms:
Definition:	A dysostosis that is characterized by characterized by multiple joint fusions, usually commencing in the hands, conductive deafness, and characteristic facial features, including a broad, tubular-shaped nose and a thin upper vermilion. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2706969/
References:	OMIM:PS186500 ORDO:3237
Ontology:	Human Disease ( DOID:0050794 )

Relationships

is a type of:	autosomal dominant disease dysostosis autosomal dominant disease dysostosis Show first 5 Terms
has subtype:	multiple synostoses syndrome 1 multiple synostoses syndrome 2 multiple synostoses syndrome 3 multiple synostoses syndrome 4 multiple synostoses syndrome 1 multiple synostoses syndrome 2 multiple synostoses syndrome 3 multiple synostoses syndrome 4 Show first 5 Terms

OTHER multiple synostoses syndrome PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None