ODCs

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

PROTEIN INTERACTIONS: 3

3 associated genes
No signs/symptoms info

Hemoglobinopathy Toms River

Autosomal dominant methemoglobinemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HBG2 HBG2 HBG2	(0.72) (0.72) (0.52)	HBA1 HBA2 HBB

Citations in the biomedical literature:

Hemoglobinopathy Toms River		Autosomal dominant methemoglobinemia
	Synonym(s): - Transient neonatal cyanosis and anemia due to Toms River Hemoglobin		Synonym(s): - Hemoglobin M disease - Hereditary methemoglobinemia due to hemoglobin mutation - M hemoglobinopathy

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.