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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

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 (core metadata concept) SNOMED CT core
2471769016 Alcaptonuric ochronosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477705016 Pigmentation due to alkaptonuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477706015 Ochronosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477707012 Alkaptonuric ochronosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477708019 Ochronosis due to homogentisate 1,2-dioxygenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477709010 Ochronosis due to alkaptonuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2465493015 Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2465493015 Ochronosis due to homogentisate 1,2-dioxygenase deficiency (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2471769016 Alcaptonuric ochronosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2471769016 Alcaptonuric ochronosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477705016 Pigmentation due to alkaptonuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2477705016 Pigmentation due to alkaptonuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477706015 Ochronosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2477706015 Ochronosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477707012 Alkaptonuric ochronosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2477707012 Alkaptonuric ochronosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477708019 Ochronosis due to homogentisate 1,2-dioxygenase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2477708019 Ochronosis due to homogentisate 1,2-dioxygenase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2477709010 Ochronosis due to alkaptonuria en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2477709010 Ochronosis due to alkaptonuria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
157541000077113 ochronose alcaptonurique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
157541000077113 ochronose alcaptonurique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

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

This concept is not in any reference sets

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