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403276003: Acquired hypomelanosis of uncertain etiology (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771202015 Acquired hypomelanosis of uncertain etiology (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773709015 Acquired hypomelanosis of uncertain aetiology en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774995019 Acquired hypomelanosis of uncertain etiology en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4554789015 Acquired idiopathic hypomelanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1771202015 Acquired hypomelanosis of uncertain etiology (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771202015 Acquired hypomelanosis of uncertain etiology (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773709015 Acquired hypomelanosis of uncertain aetiology en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1773709015 Acquired hypomelanosis of uncertain aetiology en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774995019 Acquired hypomelanosis of uncertain etiology en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1774995019 Acquired hypomelanosis of uncertain etiology en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4554789015 Acquired idiopathic hypomelanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5984591000241117 hypomélanose acquise d'origine incertaine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5984591000241117 hypomélanose acquise d'origine incertaine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


4 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acquired hypomelanosis of uncertain etiology (disorder) Is a Acquired hypomelanotic disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Acquired hypomelanosis of uncertain etiology (disorder) Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier (core metadata concept)
Acquired hypomelanosis of uncertain etiology (disorder) Associated morphology Structure showing abnormal deposition of pigment (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired hypomelanosis of uncertain etiology (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired hypomelanosis of uncertain etiology (disorder) Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired hypomelanosis of uncertain etiology (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired hypomelanosis of uncertain etiology (disorder) Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired hypomelanosis of uncertain etiology (disorder) Occurrence Period of life between birth and death true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired hypomelanosis of uncertain etiology (disorder) Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Symmetrical progressive leucopathy Is a True Acquired hypomelanosis of uncertain etiology (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic guttate hypomelanosis Is a True Acquired hypomelanosis of uncertain etiology (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Alezzandrini syndrome (disorder) Is a True Acquired hypomelanosis of uncertain etiology (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Poliosis in Vogt-Koyanagi-Harada syndrome (disorder) Is a True Acquired hypomelanosis of uncertain etiology (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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