ODCs

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5 OMIM references -
5 associated genes
6 signs/symptoms

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Hereditary persistence of fetal hemoglobin - beta-thalassemia

Sickle cell anemia


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

Citations in the biomedical literature:

Hereditary persistence of fetal hemoglobin - beta-thalassemia		Sickle cell anemia
	Synonym(s): - HPFH - beta-thalassemia		Synonym(s): - Sickle cell disease

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare bone disease - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare hematologic disease - Rare infertility - Rare renal 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: childhood Average age of death: no data available Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: adult Type of inheritance: autosomal recessive

	External references: 5 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D000755

Hereditary persistence of fetal hemoglobin - beta-thalassemia
	Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Pallor - Splenomegaly Frequent - Anomalies of bones / skeletal anomalies - Hepatomegaly / liver enlargement (excluding storage disease)
Sickle cell anemia
(no data available)