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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
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

RPS14
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RPS14
(0.56)
APP


Citations in the biomedical literature:


Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
RPS14
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- 5q- syndrome
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.