410042009: Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder)

Descriptions:

Id Description Lang Type Status Case? Module

2465493015 Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2471769016 Alcaptonuric ochronosis en Synonym Active Entire term case insensitive SNOMED CT core module

2477705016 Pigmentation due to alkaptonuria en Synonym Active Entire term case insensitive SNOMED CT core module

2477706015 Ochronosis en Synonym Active Entire term case insensitive SNOMED CT core module

2477707012 Alkaptonuric ochronosis en Synonym Active Entire term case insensitive SNOMED CT core module

2477708019 Ochronosis due to homogentisate 1,2-dioxygenase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

2477709010 Ochronosis due to alkaptonuria en Synonym Active Entire term case insensitive SNOMED CT core module

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Is a	Degenerative disorder	false	Inferred relationship	Existential restriction modifier
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Associated morphology	Structure showing abnormal deposition of pigment	true	Inferred relationship	Existential restriction modifier	1
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Due to	Homogentisate 1,2-dioxygenase deficiency	true	Inferred relationship	Existential restriction modifier	2
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Associated morphology	Degeneration	false	Inferred relationship	Existential restriction modifier
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Is a	Disorder of pigmentation	false	Inferred relationship	Existential restriction modifier
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Is a	Skin deposits	true	Inferred relationship	Existential restriction modifier
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Is a	Disorder of skin pigmentation	true	Inferred relationship	Existential restriction modifier
Ochronosis due to homogentisate 1,2-dioxygenase deficiency	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
2465493015	Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
2471769016	Alcaptonuric ochronosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2477705016	Pigmentation due to alkaptonuria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2477706015	Ochronosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2477707012	Alkaptonuric ochronosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2477708019	Ochronosis due to homogentisate 1,2-dioxygenase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
2477709010	Ochronosis due to alkaptonuria	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module