Immunoglobulin Light Chain Amyloidosis

Immunoglobulin Light Chain Amyloidosis(来自ICD-11)

别称:

Primary Amyloidosis

Al Amyloidosis

Primary Systemic Amyloidosis

Light-Chain Amyloidosis

Hereditary Amyloid Nephropathy Due to Lysozyme Variant

Familial Amyloid Nephropathy Due to Lysozyme Variant

Hereditary Renal Amyloidosis Due to Lysozyme Variant

Familial Renal Amyloidosis Due to Lysozyme Variant

Immunoglobulin Light-Chain Amyloidosis

Immunoglobulin Deposition Disease

Primary Systemic Al Amyloidosis

Amyloidosis Primary Systemic

Immunoglobulinic Amyloidosis

Light Chain Amyloidosis

Systemic Al Amyloidosis

Primary Al Amyloidosis

Systemic Al Amyloidsis

Lysozyme Amyloidosis

Amyloidosis Primary

Alys Amyloidosis

Amyloid Al

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Immunoglobulin Light Chain Amyloidosis, also known as primary amyloidosis, is related to primary cutaneous amyloidosis and myeloma, multiple. An important gene associated with Immunoglobulin Light Chain Amyloidosis is LYZ (Lysozyme), and among its related pathways/superpathways are Binding and Uptake of Ligands by Scavenger Receptors and Ca, cAMP and Lipid Signaling. The drugs Ichthammol and Daratumumab have been mentioned in the context of this disorder. Affiliated tissues include liver and spleen, and related phenotypes are fatigue and proteinuria

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