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Hereditary persistence of fetal hemoglobin - sickle cell disease
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary persistence of fetal hemoglobin - sickle cell disease
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A

HBB
(UniProt - OMIM)
 GDAP1
(UniProt - OMIM)
HBG1
(UniProt - OMIM)
HBG2
(UniProt - OMIM)
KLF1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HBB
(0.49)
GDAP1


Citations in the biomedical literature:


Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
GDAP1



Hereditary persistence of fetal hemoglobin - sickle cell disease
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A

Synonym(s):
- HPFH - sickle cell disease
Synonym(s):
- RI-CMT type A
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic 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: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.