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Terminology chevron_right Concepts chevron_right 37200009

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Component

37200009

The component that hold information about this concept.

Fully Specified Name (FSN)

Disorder of tyrosine metabolism (disorder)

Shortest Term

Disorder of tyrosine metabolism

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Disorder of tyrosine metabolism (disorder)

SCTID: 37200009, Primitive, Active

37200009|Disorder of tyrosine metabolism (disorder)|

en Disorder of tyrosine metabolism
en Disorder of tyrosine metabolism (disorder)
en Disturbance of tyrosine metabolism

Expression

37200009 |Disorder of tyrosine metabolism (disorder)|
 <<< 237911005 |Disorder of amino acid and organic acid metabolism (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
486652014 - Disorder of tyrosine metabolism (en) View
486652014	en	Synonym (core metadata concept)	Disorder of tyrosine metabolism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2817041019 - Disorder of tyrosine metabolism (disorder) (en) View
2817041019	en	Fully specified name (core metadata concept)	Disorder of tyrosine metabolism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
62062013 - Disturbance of tyrosine metabolism (en) View
62062013	en	Synonym (core metadata concept)	Disturbance of tyrosine metabolism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
769039015 - Disturbance of tyrosine metabolism (disorder) (en) View
769039015	en	Fully specified name (core metadata concept)	Disturbance of tyrosine metabolism (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
62063015 - Disturbance of tyrosine metabolism, NOS (en) View
62063015	en	Synonym (core metadata concept)	Disturbance of tyrosine metabolism, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (208470024) - 37200009 -> 44779003 (116680003) View
116680003 \|Is a (attribute)\|	44779003 \|Disorder of amino acid metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (764853028) - 37200009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2691384024) - 37200009 -> 237911005 (116680003) View
116680003 \|Is a (attribute)\|	237911005 \|Disorder of amino acid and organic acid metabolism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (764852022) - 37200009 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
237911005 View
237911005	Disorder of amino acid and organic acid metabolism (disorder)	Disorder of amino acid and organic acid metabolism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
6483008 View
6483008	Tyrosinase-negative oculocutaneous albinism (disorder)	Tyrosinase-related oculocutaneous albinism	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
413356003 View
413356003	4-hydroxyphenylpyruvate dioxygenase deficiency (disorder)	4-hydroxyphenylpyruvate dioxygenase deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
37548006 View
37548006	Hypopigmentation-immunodeficiency disease (disorder)	Giscelli syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
56595005 View
56595005	Hypertyrosinemia (disorder)	Hypertyrosinemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
57414003 View
57414003	Tyrosinosis (disorder)	Tyrosinosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
74320008 View
74320008	Woolf's syndrome (disorder)	Woolf syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
123967008 View
123967008	Tyrosinuria (disorder)	Tyrosinuria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237921002 View
237921002	Disorder of catecholamine synthesis (disorder)	Disorder of catecholamine synthesis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
360378009 View
360378009	Homogentisate 1,2-dioxygenase deficiency (disorder)	Alkaptonuria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
360410009 View
360410009	Hepatic tyrosine aminotransferase deficiency (disorder)	Hepatic tyrosine aminotransferase deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (e9338f5f-ac5e-5317-aa83-55e3509d8007) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E70.2	TRUE	ALWAYS E70.2	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

Terminology chevron_right Concepts chevron_right 37200009

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