ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal recessive axonal neuropathy with neuromyotonia

Papillary renal cell carcinoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HINT1	(0.72)	MITF

Citations in the biomedical literature:

Autosomal recessive axonal neuropathy with neuromyotonia		Papillary renal cell carcinoma
	Synonym(s): - ARAN-NM - ARCMT2-NM - Autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia		Synonym(s): - Papillary renal cell adenocarcinoma

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare oncologic disease - Rare renal disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.