ODCs

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1 associated gene
4 signs/symptoms

COMMON GENES: 1
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 3

5 OMIM references -
5 associated genes
6 signs/symptoms

Hemoglobin C - beta-thalassemia

Hereditary persistence of fetal hemoglobin - beta-thalassemia


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

Citations in the biomedical literature:

Hemoglobin C - beta-thalassemia		Hereditary persistence of fetal hemoglobin - beta-thalassemia
	Synonym(s): - C- beta-thalassemia - HbC - beta-thalassemia		Synonym(s): - HPFH - beta-thalassemia

	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: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 5 OMIM references - No MeSH references


COMMON SIGNS	- Anaemia - Hemoglobinosis / hemoglobinopathy - Splenomegaly

Hemoglobin C - beta-thalassemia		Hereditary persistence of fetal hemoglobin - beta-thalassemia
	Very frequent - Microcytic anemia		Very frequent - Pallor Frequent - Anomalies of bones / skeletal anomalies - Hepatomegaly / liver enlargement (excluding storage disease)