ODCs

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

PROTEIN INTERACTIONS: 1

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

Methylcobalamin deficiency type cblG

Melanoma and neural system tumor syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MTR	(0.68)	CDKN2A

Citations in the biomedical literature:

Methylcobalamin deficiency type cblG		Melanoma and neural system tumor syndrome
	Synonym(s): - Functional methionine synthase deficiency type cblG		Synonym(s): - Melanoma-astrocytoma syndrome

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease - Rare neurologic disease - Rare renal disease		Classification (Orphanet): - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): (no data available)

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

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

No signs/symptoms info available.