MCID: SVR052
MIFTS: 7

Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

Categories: Neuronal diseases, Rare diseases

Aliases & Classifications for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

MalaCards integrated aliases for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency:

Name: Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency 59
Autosomal Recessive Charcot-Marie-Tooth Disease, Ouvrier Type 59
Seoan Due to Mfn2 Deficiency 59
Ar-Cmt2, Ouvrier Type 59

Classifications:

Orphanet: 59  
Rare neurological diseases


External Ids:

Orphanet 59 ORPHA90118
ICD10 via Orphanet 34 G60.0

Summaries for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

MalaCards based summary : Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency, is also known as autosomal recessive charcot-marie-tooth disease, ouvrier type. An important gene associated with Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency is MFN2 (Mitofusin 2).

Related Diseases for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

Symptoms & Phenotypes for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

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Variations for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

Expression for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

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GO Terms for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

Sources for Severe Early-Onset Axonal Neuropathy Due to Mfn2 Deficiency

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