Neuropathy, ataxia, and retinitis pigmentosa

Description

Neuropathy, Ataxia, and Retinitis Pigmentosa (NARP) syndrome is a clinically heterogeneous oxidative phosphorylation disorder often characterised by a combination of sensory-motor neuropathy, cerebellar ataxia, and night blindness.

Index terms

Neuropathy, ataxia, and retinitis pigmentosa
NARP - [Neuropathy, ataxia and retinitis pigmentosa] syndrome
Neurogenic muscle weakness, ataxia, and retinitis pigmentosa

Exclusions from above levels

http://id.who.int/icd/entity/155258022 – Metabolic disorders
LD26.41 – Arthrogryposis multiplex congenita
05 – Endocrine, nutritional or metabolic diseases

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18 – Complications of pregnancy, childbirth and the puerperium
19 – Certain conditions originating in the perinatal period
22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

8C73.0 – Autosomal recessive cardiomyopathy or ophthalmoplegia
8C73.Y – Other specified mitochondrial myopathies
8C73.Z – Mitochondrial myopathies, unspecified

Foundation entity

Neuropathy, ataxia, and retinitis pigmentosa – http://id.who.int/icd/entity/2089784682

Part of: 8C73: Mitochondrial myopathies › 08: Diseases of the nervous system