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


Status: current, Primitive. 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 Case insensitive SNOMED CT core
2471769016 Alcaptonuric ochronosis en Synonym Active Case insensitive SNOMED CT core
2477705016 Pigmentation due to alkaptonuria en Synonym Active Case insensitive SNOMED CT core
2477706015 Ochronosis en Synonym Active Case insensitive SNOMED CT core
2477707012 Alkaptonuric ochronosis en Synonym Active Case insensitive SNOMED CT core
2477708019 Ochronosis due to homogentisate 1,2-dioxygenase deficiency en Synonym Active Case insensitive SNOMED CT core
2477709010 Ochronosis due to alkaptonuria en Synonym Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Alcaptonuric ochronosis Is a Skin deposits true Inferred relationship Some
Alcaptonuric ochronosis Is a Disorder of skin pigmentation true Inferred relationship Some
Alcaptonuric ochronosis Finding site Skin structure true Inferred relationship Some 1
Alcaptonuric ochronosis Is a Degenerative disorder false Inferred relationship Some
Alcaptonuric ochronosis Associated morphology Pigment deposition true Inferred relationship Some 1
Alcaptonuric ochronosis Due to Homogentisate 1,2-dioxygenase deficiency true Inferred relationship Some 2
Alcaptonuric ochronosis Associated morphology Degeneration false Inferred relationship Some
Alcaptonuric ochronosis Is a Disorder of pigmentation false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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