ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Charcot-Marie-Tooth disease type 4D

Familial gastric cancer

NDRG1	(UniProt - OMIM)		CDH1	(UniProt - OMIM)
			MUTYH	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	NDRG1	(0.74)	CDH1

Citations in the biomedical literature:

Charcot-Marie-Tooth disease type 4D		Familial gastric cancer
	Synonym(s): - CMT4D - HMSN, Lom type - Hereditary motor and sensory neuropathy, Lom type		Synonym(s): - Familial stomach cancer

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial

	External references: 1 OMIM reference - 1 MeSH reference: C535716		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.