Hereditary Transthyretin Amyloidosis

Alias:

Hereditary Attr Amyloidosis

Familial Amyloid Polyneuropathy

Hereditary Amyloid Polyneuropathy Portuguese Type

Familial Amyloid Polyneuropathy, 30 Met-for-Val

Familial Amyloid Neuropathy, Portuguese Type

Portuguese Type Familial Amyloid Neuropathy

Familial Transthyretin-Related Amyloidosis

Familial Amyloid Neuropathy, Andrade Type

Hereditary Neuropathic Amyloidosis Type 1

Type Ii Familial Amyloid Polyneuropathy

Fap - [familial Amyloid Polyneuropathy]

Type I Familial Amyloid Polyneuropathy

Neuropathic Heredofamilial Amyloidosis

Portuguese Type Amyloid Polyneuropathy

Familial Polyneuropathic Amyloidosis

Japanese Type Amyloid Polyneuropathy

Portuguese Polyneuritic Amyloidosis

Andrade Type Amyloid Polyneuropathy

Swedish Type Amyloid Polyneuropathy

Familial Transthyretin Amyloidosis

Swiss Type Amyloid Polyneuropathy

Transthyretin-Related Amyloidosis

Portuguese Amyloid Polyneuropathy

Familial Ttr-Related Amyloidosis

Familial Neuropathic Amyloidosis

Corino De Andrade Paramyloidosis

Wohlwill-Corino Andrade Syndrome

Amyloid Polyneuropathy Type 1

Polyneuropathy in Amyloidosis

Amyloid Polyneuropathy

Portuguese Amyloidosis

Af Type Amyloidosis

Amyloidosis Type 1

Andrade Syndrome

Paramyloidosis

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Hereditary Transthyretin Amyloidosis, also known as hereditary attr amyloidosis, is related to amyloidosis, finnish type and lattice corneal dystrophy. The drugs Immunoglobulins and Immunoglobulins, Intravenous have been mentioned in the context of this disorder. Affiliated tissues include heart and bone.

Related ID：

MALACARDS：HRD207

ICD11：807065795