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79644001: Pigment alteration (morphologic abnormality)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
132132010 Pigment alteration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
820717016 Pigment alteration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
45861000052110 pigmentförändring sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


39 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pigment alteration Is a Morphologically abnormal structure (morphologic abnormality) false Inferred relationship Some
Pigment alteration Is a Lesion (morphologic abnormality) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
McCune Albright syndrome (disorder) Associated morphology False Pigment alteration Inferred relationship Some 7
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome Associated morphology False Pigment alteration Inferred relationship Some 3
Familial progressive hyper and hypopigmentation Associated morphology False Pigment alteration Inferred relationship Some 2
Familial progressive hyper and hypopigmentation Associated morphology True Pigment alteration Inferred relationship Some 1
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome Associated morphology True Pigment alteration Inferred relationship Some 2
McCune Albright syndrome (disorder) Associated morphology True Pigment alteration Inferred relationship Some 2
Flat birthmark Associated morphology True Pigment alteration Inferred relationship Some 2
Raised birthmark Associated morphology True Pigment alteration Inferred relationship Some 1
Birthmark Associated morphology True Pigment alteration Inferred relationship Some 1
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) Associated morphology True Pigment alteration Inferred relationship Some 3
Vascular birthmark Associated morphology True Pigment alteration Inferred relationship Some 1
Pigmentation of skin caused by artificial ultraviolet light (finding) Associated morphology True Pigment alteration Inferred relationship Some 1
Pigmented skin lesion of uncertain nature of head Associated morphology True Pigment alteration Inferred relationship Some 1
Pigmented skin lesion of uncertain nature of trunk Associated morphology True Pigment alteration Inferred relationship Some 1
Pigmented skin lesion of uncertain nature of upper limb Associated morphology True Pigment alteration Inferred relationship Some 1
Pigmented skin lesion of uncertain nature of neck (disorder) Associated morphology True Pigment alteration Inferred relationship Some 1
Conjunctival pigmentation Associated morphology True Pigment alteration Inferred relationship Some 1
Conjunctival pigmentation of right eye Associated morphology True Pigment alteration Inferred relationship Some 1
Conjunctival pigmentation of left eye (disorder) Associated morphology True Pigment alteration Inferred relationship Some 1
Bilateral conjunctival pigmentation of eyes Associated morphology True Pigment alteration Inferred relationship Some 1
Bilateral conjunctival pigmentation of eyes Associated morphology True Pigment alteration Inferred relationship Some 2
café-au-lait-fläckar och ringkromosom 11 Associated morphology False Pigment alteration Inferred relationship Some 2
Gingival pigmentation (disorder) Associated morphology True Pigment alteration Inferred relationship Some 1

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