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57174000: Focal amyloid (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
95091013 Focal amyloid en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
95092018 Nodular amyloid en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
795767017 Focal amyloid (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3027401000005115 fokal amyloid da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Focal amyloid Is a Amyloid deposition true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Pulmonary amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloidosis of skin Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid of cornea (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid of vitreous Associated morphology False Focal amyloid Inferred relationship Some 1
Laryngeal amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloidosis of spleen Associated morphology False Focal amyloid Inferred relationship Some
Hereditary cerebrovascular amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
Localised hereditary amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Familial lichen amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Papuløs kutan amyloid Associated morphology False Focal amyloid Inferred relationship Some 1
Poikilodermal cutaneous amyloid Associated morphology False Focal amyloid Inferred relationship Some 1
Localised non-hereditary amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Macular cutaneous amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 2
Dominant primary localized cutaneous amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
lokaliseret amyloidaflejring Associated morphology False Focal amyloid Inferred relationship Some 1
Gingival amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloid of urinary bladder (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
AD-amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid of prostate Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid of testes Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid of ureter Associated morphology False Focal amyloid Inferred relationship Some 2
Kutan amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Familial amyloid nephropathy with urticaria AND deafness Associated morphology False Focal amyloid Inferred relationship Some
Bullous cutaneous amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
Isolated atrial amyloid Associated morphology False Focal amyloid Inferred relationship Some
Isolated corneal amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
Hereditary oculoleptomeningeal amyloid angiopathy Associated morphology False Focal amyloid Inferred relationship Some 2
Cerebrovaskulær amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology False Focal amyloid Inferred relationship Some 3
Senile brain amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 2
Amyloid nephropathy Associated morphology False Focal amyloid Inferred relationship Some
Hereditary cerebral amyloid angiopathy, Dutch type Associated morphology False Focal amyloid Inferred relationship Some 1
Localized amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Familial visceral amyloidosis, Ostertag type Associated morphology False Focal amyloid Inferred relationship Some
Ocular amyloid deposit Associated morphology False Focal amyloid Inferred relationship Some
Autonomic neuropathy due to amyloidosis Associated morphology False Focal amyloid Inferred relationship Some
Polyneuropathy due to amyloidosis (disorder) Associated morphology False Focal amyloid Inferred relationship Some
neuropati ved sekundær amyloidose Associated morphology False Focal amyloid Inferred relationship Some
Primær systemisk (AL fibril-type) amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid light chain amyloidosis due to multiple myeloma (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Primary systemic amyloidosis associated with occult plasma cell dyscrasia Associated morphology False Focal amyloid Inferred relationship Some 1
Macroglossia due to amyloidosis (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Pseudoscleroderma due to amyloid light-chain amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
Secondary systemic amyloidosis affecting skin (AA fibril type) (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Hemodialysis-associated secondary amyloidosis of skin (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Heredofamilial systemic amyloidosis affecting skin (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Makulopapuløs amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Nodulær amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Familial localized cutaneous amyloidosis (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Secondary localized cutaneous amyloidosis (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Systemic amyloidosis affecting skin (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloidosis limited to skin (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid corneal degeneration (disorder) Associated morphology False Focal amyloid Inferred relationship Some 2
Amyloid light-chain nephropathy (disorder) Associated morphology False Focal amyloid Inferred relationship Some
AA amyloid nephropathy Associated morphology False Focal amyloid Inferred relationship Some
Kutan amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Hereditary cerebrovascular amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Papuløs kutan amyloid Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloid of urinary bladder (disorder) Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloid of cornea (disorder) Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloidosis limited to skin (disorder) Associated morphology True Focal amyloid Inferred relationship Some 1
Dominant primary localized cutaneous amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloid of testes Associated morphology True Focal amyloid Inferred relationship Some 1
Laryngeal amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Familial localized cutaneous amyloidosis (disorder) Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloid of prostate Associated morphology True Focal amyloid Inferred relationship Some 1
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Makulopapuløs amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Secondary systemic amyloidosis affecting skin (AA fibril type) (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
AD-amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Amyloidosis of skin Associated morphology False Focal amyloid Inferred relationship Some 1
Hereditary cerebral amyloid angiopathy, Dutch type Associated morphology False Focal amyloid Inferred relationship Some 1
Primary systemic amyloidosis associated with occult plasma cell dyscrasia Associated morphology False Focal amyloid Inferred relationship Some 2
Hemodialysis-associated secondary amyloidosis of skin (disorder) Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloid light chain amyloidosis due to multiple myeloma (disorder) Associated morphology False Focal amyloid Inferred relationship Some 2
Pseudoscleroderma due to amyloid light-chain amyloidosis Associated morphology False Focal amyloid Inferred relationship Some 1
Poikilodermal cutaneous amyloid Associated morphology True Focal amyloid Inferred relationship Some 1
Pulmonary amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloid corneal degeneration (disorder) Associated morphology False Focal amyloid Inferred relationship Some 2
Heredofamilial systemic amyloidosis affecting skin (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Secondary localized cutaneous amyloidosis (disorder) Associated morphology True Focal amyloid Inferred relationship Some 1
Isolated corneal amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Bullous cutaneous amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1
Amyloid of vitreous Associated morphology True Focal amyloid Inferred relationship Some 1
Primær systemisk (AL fibril-type) amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Nodulær amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Systemic amyloidosis affecting skin (disorder) Associated morphology False Focal amyloid Inferred relationship Some 1
Cerebrovaskulær amyloidose Associated morphology False Focal amyloid Inferred relationship Some 1
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology True Focal amyloid Inferred relationship Some 1
Hereditary cerebral amyloid angiopathy, Dutch type Associated morphology True Focal amyloid Inferred relationship Some 2
Primary localized cutaneous nodular amyloidosis (PLCNA) is the most rare form of primary cutaneous amyloidosis, a skin disease characterized by the accumulation of amyloid deposits in the dermis, characterized clinically by yellowish waxy crusted nodules and papules on the face, lower extremities, trunk, scalp, and genitalia and histologically by the localized deposition of immunoglobulin-derived amyloid in the papillary dermis and subcutis. PLCNA can be associated with connective tissue disorders such as Sjögren's syndrome and CREST syndrome. Associated morphology True Focal amyloid Inferred relationship Some 1
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. Associated morphology True Focal amyloid Inferred relationship Some 2
A rare genetic cerebral small vessel disease characterized by amyloid deposition in the cerebral blood vessels leading to predominantly hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia. Associated morphology False Focal amyloid Inferred relationship Some 2
Primary localized cutaneous amyloidosis (disorder) Associated morphology True Focal amyloid Inferred relationship Some 1
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. Associated morphology True Focal amyloid Inferred relationship Some 1
A rare systemic amyloidosis with characteristics of a triad of ophthalmologic, neurologic and dermatologic findings due to the deposition of gelsolin amyloid fibrils in these tissues. Clinical manifestations include corneal lattice dystrophy, cranial neuropathy, especially affecting the facial nerve, bulbar signs, cutis laxa, increased skin fragility and less commonly peripheral neuropathy and renal failure. Caused by mutation in the gelsolin gene (GSN). Associated morphology True Focal amyloid Inferred relationship Some 2
Lattice corneal dystrophy Type I (disorder) Associated morphology True Focal amyloid Inferred relationship Some 2
Lattice corneal dystrophy (disorder) Associated morphology True Focal amyloid Inferred relationship Some 2
Amyloid of ureter Associated morphology True Focal amyloid Inferred relationship Some 1
Senile brain amyloidosis Associated morphology True Focal amyloid Inferred relationship Some 1

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