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Delta-beta-thalassemia
1 OMIM reference -
3 associated genes
46 connected diseases
3 signs/symptoms
Disease Type of connection
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Hereditary persistence of fetal hemoglobin - sickle cell disease
Hemoglobin Lepore - beta-thalassemia
Autosomal dominant methemoglobinemia
Beta-thalassemia intermedia
Beta-thalassemia major
Dominant beta-thalassemia
Heinz body anemia
Hemoglobin C - beta-thalassemia
Hemoglobin C disease
Hemoglobin D disease
Hemoglobin E - beta-thalassemia
Hemoglobin E disease
Sickle cell - beta-thalassemia disease
Sickle cell - hemoglobin C disease
Sickle cell - hemoglobin D disease
Sickle cell - hemoglobin E disease
Sickle cell anemia
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16
Hb Bart's hydrops fetalis
Hemoglobin H disease
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Hemoglobinopathy Toms River
Autosomal agammaglobulinemia
Cowden syndrome
Familial isolated dilated cardiomyopathy
Huntington disease
Juvenile Huntington disease
Muscular dystrophy, Selcen type
Proteus syndrome
Richieri Costa-Pereira syndrome
Thrombocytopenia - absent radius
X-linked Emery-Dreifuss muscular dystrophy
Autosomal dominant Charcot-Marie-Tooth disease type 2K
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
Charcot-Marie-Tooth disease type 2H
Charcot-Marie-Tooth disease type 4A
X-linked intellectual deficit with marfanoid habitus
X-linked non-syndromic intellectual deficit
Synonym(s):
(no synonyms)

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 -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
HBB P68871141900
HBD P02042142000
HBG1 P69891142200
Very frequent
- Anaemia
- Hemoglobinosis / hemoglobinopathy
- Microcytic anemia