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

Hypermethioninemia due to glycine N-methyltransferase deficiency

Familial isolated congenital asplenia

GNMT	(UniProt - OMIM)		NKX2-5	(UniProt - OMIM)
			RPSA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GNMT	(0.63)	RPSA

Citations in the biomedical literature:

Hypermethioninemia due to glycine N-methyltransferase deficiency		Familial isolated congenital asplenia
	Synonym(s): - Glycine N-methyltransferase deficiency - Hypermethioninemia due to GNMT deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease		Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.