Cytoscape Web
Click node...

Familial isolated congenital asplenia
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary persistence of fetal hemoglobin - sickle cell disease
4 associated genes
No signs/symptoms info
Familial isolated congenital asplenia
Hereditary persistence of fetal hemoglobin - sickle cell disease

NKX2-5
(UniProt - OMIM)
 HBB
(UniProt - OMIM)
RPSA
(UniProt - OMIM)
 HBG1
(UniProt - OMIM)
HBG2
(UniProt - OMIM)
KLF1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RPSA
(0.63)
HBG2


Citations in the biomedical literature:


Familial isolated congenital asplenia
NKX2-5 RPSA
Hereditary persistence of fetal hemoglobin - sickle cell disease
HBB HBG1 HBG2 KLF1



Familial isolated congenital asplenia
Hereditary persistence of fetal hemoglobin - sickle cell disease

Synonym(s):
(no synonyms)

Synonym(s):
- HPFH - sickle cell disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.