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1 OMIM reference -
3 associated genes
3 signs/symptoms
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Delta-beta-thalassemia
X-linked Emery-Dreifuss muscular dystrophy

HBB EMD
HBD FHL1
HBG1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HBD
(0.63)
EMD



Citations in the biomedical literature:


Delta-beta-thalassemia
HBB HBD HBG1
X-linked Emery-Dreifuss muscular dystrophy
EMD FHL1



Delta-beta-thalassemia
X-linked Emery-Dreifuss muscular dystrophy

Synonym(s):
(no synonyms)

Synonym(s):
- EDMD1

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare cardiac disease
- 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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: x-linked recessive

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

Delta-beta-thalassemia

Very frequent
- Anaemia
- Hemoglobinosis / hemoglobinopathy
- Microcytic anemia



X-linked Emery-Dreifuss muscular dystrophy

(no data available)