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Dominant beta-thalassemia

1 OMIM reference -
1 associated gene
6 signs/symptoms

PROTEIN INTERACTIONS: 1

Juvenile Huntington disease

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

Dominant beta-thalassemia

Juvenile Huntington disease

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HBB	(0.63)	HTT

Citations in the biomedical literature:

Dominant beta-thalassemia		Juvenile Huntington disease
	Synonym(s): - Inclusion body beta-thalassemia		Synonym(s): - JHD - Juvenile Huntington chorea

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adolescence / young 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

Dominant beta-thalassemia
	Very frequent - Anaemia - Hemoglobinosis / hemoglobinopathy - Hepatitis / icterus / cholestasis - Microcytic anemia - Pallor - Splenomegaly
Juvenile Huntington disease
(no data available)