Amyloidosis, Finnish Type (AMYL5)

Amyloidosis, Finnish Type(来自ICD-11)

别称:

Finnish Type Amyloidosis

Meretoja Syndrome

Familial Amyloid Polyneuropathy Type Iv

Familial Amyloidosis, Finnish Type

Lattice Corneal Dystrophy Type Ii

Gelsolin Amyloidosis

Amyloid Cranial Neuropathy with Lattice Corneal Dystrophy

Amyloidosis Due to Mutant Gelsolin

Amyloidosis, Meretoja Type

Agel Amyloidosis

Amyloidosis V

Hereditary Amyloidosis, Finnish Type

Lattice Corneal Dystrophy, Gelsolin Type

Familial Amyloid Polyneuropathy, Type Iv

Type Iv Familial Amyloid Polyneuropathy

Familial Amyloid Polyneuropathy, Type V

Familial Amyloidosis Finnish Type

Lattice Corneal Dystrophy Type 2

Gelsolin-Related Amyloidosis

Meretoja Type Amyloidosis

Kymenlaakso Syndrome

Amyloidosis 5

Amyl5

Agel

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Amyloidosis, Finnish Type, also known as finnish type amyloidosis, is related to recurrent corneal erosion and hereditary amyloidosis, and has symptoms including corneal lattice dystrophy, bilateral facial paralysis and cutis laxa. An important gene associated with Amyloidosis, Finnish Type is GSN (Gelsolin), and among its related pathways/superpathways are Metabolism of proteins and RNA Polymerase I Promoter Opening. Affiliated tissues include skin and eye, and related phenotypes are dry skin and abnormality of the eye

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