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79644001: Pigment alteration (morphologic abnormality)

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

Descriptions:

Id Description Lang Type Status Case? Module
132132010 Pigment alteration en Synonym Active Entire term case insensitive SNOMED CT core module
820717016 Pigment alteration (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

39 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pigment alteration Is a Morphologically abnormal structure false Inferred relationship Existential restriction modifier
Pigment alteration Is a Lesion true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
McCune Albright syndrome Associated morphology False Pigment alteration Inferred relationship Existential restriction modifier 7
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome Associated morphology False Pigment alteration Inferred relationship Existential restriction modifier 3
Familial progressive hyperpigmentation and hypopigmentation of skin Associated morphology False Pigment alteration Inferred relationship Existential restriction modifier 2
Familial progressive hyperpigmentation and hypopigmentation of skin Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 2
McCune Albright syndrome Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 2
Flat birthmark Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 2
Raised birthmark Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Birthmark Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 3
Vascular birthmark Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmentation of skin caused by artificial ultraviolet light Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmented skin lesion of uncertain nature of head Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmented skin lesion of uncertain nature of trunk Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmented skin lesion of uncertain nature of upper limb Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmented skin lesion of uncertain nature of neck Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Conjunctival pigmentation Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Conjunctival pigmentation of right eye Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Conjunctival pigmentation of left eye Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Conjunctival pigmentation of bilateral eyes Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Conjunctival pigmentation of bilateral eyes Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 2
Café-au-lait spots and ring chromosome 11 Associated morphology False Pigment alteration Inferred relationship Existential restriction modifier 2
Gingival pigmentation Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmentary disturbance of oral mucosa Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Laser-induced dyspigmentation Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 6
Punctate acrokeratoderma freckle-like pigmentation Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 3
Disorder of pigmentation of skin following cosmetic surgery Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmented skin lesion of uncertain nature of lower extremity Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Pigmented lesion of skin of lower limb Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Terra firma-forme dermatosis Associated morphology True Pigment alteration Inferred relationship Existential restriction modifier 1
Congenital pigmentary skin anomaly NOS Associated morphology False Pigment alteration Inferred relationship Existential restriction modifier 2
Dyschromia NOS Associated morphology False Pigment alteration Inferred relationship Existential restriction modifier 1

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