C0002768 - A very rare, autosomal recessive inherited condition caused by mutations in the SCN9A gene. It is characterized by a lack of the ability to perceive physical pain.

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Lang Dictionary CODE			LUI	preferred no	SUI	preference Yes / No	Terms, descriptions
							CUI C0002768

Russian	Medical Subject Headings Russian	D000699	L3341479	preferred	S3868960	Y	БОЛЕВАЯ НЕЧУВСТВИТЕЛЬНОСТЬ ВРОЖДЕННАЯ
Russian	Medical Subject Headings Russian	D000699	L0891416	no	S1095233	Y	BOLEVAIA NECHUVSTVITEL'NOST' VROZHDENNAIA
Russian	Medical Subject Headings Russian	D000699	L1508467	no	S1804376	Y	ANALGEZIIA VROZHDENNAIA
Russian	Medical Subject Headings Russian	D000699	L1532534	no	S1828443	Y	NECHUVSTVITEL'NOST' K BOLI VROZHDENNAIA
Russian	Medical Subject Headings Russian	D000699	L3338259	no	S3865740	Y	АНАЛГЕЗИЯ ВРОЖДЕННАЯ
Russian	Medical Subject Headings Russian	D000699	L3360148	no	S3887635	Y	НЕЧУВСТВИТЕЛЬНОСТЬ К БОЛИ ВРОЖДЕННАЯ
	Medical Subject Headings				A0096866	AT187617899	A syndrome characterized by indifference to PAIN despite the ability to distinguish noxious from non-noxious stimuli. Absent corneal reflexes and INTELLECTUAL DISABILITY may be associated. Familial forms with autosomal recessive and autosomal dominant patterns of inheritance have been described. (Adams et al., Principles of Neurology, 6th ed, p1343)
	NCI Thesaurus				A26702025	AT213845397	A very rare, autosomal recessive inherited condition caused by mutations in the SCN9A gene. It is characterized by a lack of the ability to perceive physical pain.