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733729003: Primary localized cutaneous amyloidosis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3473432011 Primary localized cutaneous amyloidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3473433018 Primary localized cutaneous amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3473434012 Primary localised cutaneous amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3473432011 Primary localized cutaneous amyloidosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3473433018 Primary localized cutaneous amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3473434012 Primary localised cutaneous amyloidosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3435481001000110 Primäre kutane Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6445991000241118 amyloïdose cutanée primitive localisée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6446001000241119 amylose cutanée primitive localisée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6446011000241117 ACPL - amylose cutanée primitive localisée fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6445991000241118 amyloïdose cutanée primitive localisée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6446001000241119 amylose cutanée primitive localisée fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6446011000241117 ACPL - amylose cutanée primitive localisée fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3435481001000110 Primäre kutane Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary localized cutaneous amyloidosis (disorder) Is a Amyloidosis of skin true Inferred relationship Existential restriction modifier (core metadata concept)
Primary localized cutaneous amyloidosis (disorder) Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary localized cutaneous amyloidosis (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Maculopapular amyloidosis Is a False Primary localized cutaneous amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Familial localized cutaneous amyloidosis (disorder) Is a True Primary localized cutaneous amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Primary localized cutaneous nodular amyloidosis Is a True Primary localized cutaneous amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Lichen amyloidosis is a rare chronic form of cutaneous amyloidosis, a skin disease characterized by the accumulation of amyloid deposits in the dermis, clinically characterized by the development of pruritic, often pigmented, hyperkeratotic papules on trunk and extremities, especially on the shins, and histologically by the deposition of amyloid or amyloid-like proteins in the papillary dermis. Is a True Primary localized cutaneous amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare primary cutaneous amyloidosis characterized by macular or reticulate hyperpigmentation with symmetrically distributed guttate hypo- and hyperpigmented lesions which progress gradually over the years to involve almost the entire body (with relative sparing of the face, hands, feet and neck). Patients are usually asymptomatic, however mild pruritus may be associated. Amyloid deposition in the papillary dermis is observed on skin biopsy. Systemic amyloidosis is not present and association with generalized morphea, atypical Parkinsonism, spasticity, motor weakness or colon carcinoma is rare. Is a True Primary localized cutaneous amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Macular cutaneous amyloidosis Is a True Primary localized cutaneous amyloidosis (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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