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51083003: Structure showing abnormal deposition of pigment (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
85116019 Pigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85118018 Pigment deposition en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
788943015 Structure showing abnormal deposition of pigment (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2670935014 Structure showing abnormal deposition of pigment en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85116019 Pigmentation en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
85116019 Pigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
85118018 Pigment deposition en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
85118018 Pigment deposition en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
788943015 Structure showing abnormal deposition of pigment (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
788943015 Structure showing abnormal deposition of pigment (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2670935014 Structure showing abnormal deposition of pigment en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2670935014 Structure showing abnormal deposition of pigment en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


36 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Structure showing abnormal deposition of pigment (morphologic abnormality) Is a Deposition true Inferred relationship Existential restriction modifier (core metadata concept)
Structure showing abnormal deposition of pigment (morphologic abnormality) Is a Pigment alteration true Inferred relationship Existential restriction modifier (core metadata concept)
Structure showing abnormal deposition of pigment (morphologic abnormality) Is a Lesion of degenerative abnormality (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Xanthosis (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Fibrosiderotic nodule Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Heavy metal pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Ferrocalcinotic deposition Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Haematin pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Hematoidin pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Melanosis Is a False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Hyperpigmentation (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Melanin pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Lipochrome pigmentation (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Hemosiderin pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Hemofuscin pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Bile pigmentation (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Kernicterus (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Mineralized neurons (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Pseudomelanosis (morphologic abnormality) Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Lipogenic pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Ceroid pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Hemoglobin pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Porphyrin pigmentation Is a True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Hypopigmentation disorder Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Villonodular synovitis of multiple sites Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group B Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
pigmentation paludéenne Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Malarial pigment deposition (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) Associated morphology True Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Drug-induced pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Drug pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Schistosomal pigment deposition Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Occupational tattoo Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Collier's stripes Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Occupational vitiligo Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudoatrophoderma colli Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Drug-induced hypomelanosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical progressive leucopathy Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acantholytic dyskeratotic epidermal nevus Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Nevus striatus symmetricus of thumbs Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Epidermal nevus syndrome Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Miscellaneous disorders of skin pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Mucosal lentiginosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmentation of fingers (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
A rare type of keratinopathic ichthyosis characterised by the presence of severe hyperkeratotic lesions and palmoplantar keratoderma. The skin is usually normal at birth. The disease starts in early childhood with severe hyperkeratosis of yellow-brown or grey colour, and of spiky, cobblestone-like (hystrix) or verrucous appearance. Contrary to other keratinopathic ichthyoses, no skin fragility/blister formation or erythroderma is present. The disease results from heterozygous frameshift mutation in a section of the KRT1 gene encoding keratin 1 (K1). These mutations lead to an abnormal supramolecular organisation of keratin intermediate filaments and may be related to defects in cytoplasmic trafficking and integrity of cellular structures such as organelles and nucleus. Transmission is autosomal dominant but some sporadic cases have been reported. Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Ichthyosis hystrix Bäfverstedt type (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Ichthyosis hystrix gravior of Rheydt Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Hystrix ichthyosis with deafness Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Porcupine man Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
De Sanctis-Cacchione syndrome Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired disorder of skin colour Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Post-inflammatory hypopigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chemically-induced hypomelanosis (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Diffuse tenosynovial giant cell tumor of lower limb Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Café au lait spots Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmented xerodermoid Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic guttate hypomelanosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Anterior corneal pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Chlorpromazine pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Skin hypopigmented Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Achromia of skin Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
ictère périnatal causé par une hémolyse excessive Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Xeroderma pigmentosum, group C (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group G Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Progressive pigmentary dermatosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Leukoderma Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Xeroderma pigmentosum, group F Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Tattoo granuloma Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 5
Xeroderma pigmentosum, group A Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Dubin-Johnson syndrome Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Xeroderma pigmentosum (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Poikiloderma of Civatte Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Disorder of skin pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Linear sebaceous nevus sequence Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Conjunctival argyrosis Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Stromal corneal pigmentation Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Syphilitic leukoderma Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group E (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Vitiligo of pinta (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 3
Vitiligo Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
ictère périnatal dû à une anémie hémolytique héréditaire Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Hemolytic jaundice Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Progressive pigmentary dermatosis of Schamberg Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Conjunctival pigmentation (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Ichthyosis hystrix (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, group D Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal jaundice due to delayed conjugation from delayed development of conjugating system (finding) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Ephelides Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Nevus unius lateris Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 5
Disorder of central nervous system due to xeroderma pigmentosum (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal jaundice associated with preterm delivery (finding) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Perinataler Ikterus verursacht durch Gallenpfropf-Syndrom Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
Tattoo Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-neurologic xeroderma pigmentosum Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Erythromelanosis follicularis of face AND/OR neck (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Vitiligo of eyelid (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Xeroderma pigmentosum, variant form Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Argyria of skin Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Neurofibromatosis type 1 (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Postinflammatory skin pigmentation change Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Application site pigmentation changes Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept)
synovite villonodulaire pigmentée Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired anterior capsular pigmentation (disorder) Associated morphology False Structure showing abnormal deposition of pigment (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1

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