C0016037 - An autosomal recessive disorder of connective tissue caused by mutation(s) in the ACVR1 gene, encoding activin receptor type-1. This condition is characterized by congenital malformations of the great toes and progressive ossification of skeletal muscle, fascia, tendons, and ligaments.

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Lang Dictionary CODE			LUI	preferred no	SUI	preference Yes / No	Terms, descriptions
							CUI C0016037

Russian	MDRRUS	10068715	L15783994	preferred	S19071659	N	Прогрессирующая оссифицирующая фибродисплазия
Russian	MDRRUS	10068715	L15783994	preferred	S19071659	Y	Прогрессирующая оссифицирующая фибродисплазия
Russian	MDRRUS	10036809	L15728778	no	S19071670	Y	Прогрессирующий оссифицирующий миозит
	(CPTSP) CRISP Thesaurus				A1308201	AT51221804	disease characterized by bony deposits or the ossification of muscle tissue.
	NCI Thesaurus				A7570565	AT220002683	A condition in which there is progressive heterotopic bone formation of the tendons and muscles.
	NCI National Institute of Child Health and Human Development				A7570565	AT224187052	An autosomal recessive disorder of connective tissue caused by mutation(s) in the ACVR1 gene, encoding activin receptor type-1. This condition is characterized by congenital malformations of the great toes and progressive ossification of skeletal muscle, fascia, tendons, and ligaments.