Cytoscape Web
Click node...

Hemoglobin H disease
1 OMIM reference -
2 associated genes
63 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant methemoglobinemia
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16
Hb Bart's hydrops fetalis
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Hereditary persistence of fetal hemoglobin - sickle cell disease
Hemoglobin Lepore - beta-thalassemia
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
Apolipoprotein A-I deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant
Hemoglobinopathy Toms River
Leber congenital amaurosis
Primary systemic amyloidosis
Senior-Loken syndrome
CLN10 disease
Angelman syndrome
Autoimmune lymphoproliferative syndrome
Autosomal dominant distal renal tubular acidosis
Autosomal recessive systemic lupus erythematosus
Bannayan-Riley-Ruvalcaba syndrome
Common variable immunodeficiency
Congenital analbuminemia
Cowden syndrome
Distal renal tubular acidosis with anemia
Familial partial lipodystrophy due to AKT2 mutations
Fibronectin glomerulopathy
Giant cell glioblastoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Hereditary breast and ovarian cancer syndrome
Hereditary spherocytosis
Hypoinsulinemic hypoglycemia and body hemihypertrophy
Isolated focal cortical dysplasia type IIb
Juvenile polyposis of infancy
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Pediatric systemic lupus erythematosus
Pontocerebellar hypoplasia type 1
Proteus syndrome
Proteus-like syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Southeast Asian ovalocytosis
Squamous cell carcinoma of head and neck
Tuberous sclerosis
Familial isolated dilated cardiomyopathy
Fatal infantile hypertonic myofibrillar myopathy
Posterior polar cataract
Zonular cataract
- Alpha-thalassemia intermedia
- HbH disease

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

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

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
HBA1 P69905141800
HBA2 P69905141850
No signs/symptoms info available.