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Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial isolated congenital asplenia
1 OMIM reference -
2 associated genes
No signs/symptoms info
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Familial isolated congenital asplenia

RPS14
(UniProt - OMIM)
 NKX2-5
(UniProt - OMIM)
RPSA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RPS14
(0.49)
RPSA


Citations in the biomedical literature:


Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
RPS14
Familial isolated congenital asplenia
NKX2-5 RPSA



Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Familial isolated congenital asplenia

Synonym(s):
- 5q- syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.