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Hereditary persistence of fetal hemoglobin - sickle cell disease
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
2 associated genes
No signs/symptoms info
Hereditary persistence of fetal hemoglobin - sickle cell disease
Acute myeloid leukemia with t(8;16)(p11;p13) translocation

HBB
(UniProt - OMIM)
 CREBBP
(UniProt - OMIM)
HBG1
(UniProt - OMIM)
 KAT6A
(UniProt - OMIM)
HBG2
(UniProt - OMIM)
KLF1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KLF1
(0.8)
CREBBP


Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
CREBBP KAT6A



Hereditary persistence of fetal hemoglobin - sickle cell disease
Acute myeloid leukemia with t(8;16)(p11;p13) translocation

Synonym(s):
- HPFH - sickle cell disease
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.