Cytoscape Web
Click node...

Atypical hemolytic uremic syndrome with H factor anomaly
2 OMIM references -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute promyelocytic leukemia
1 OMIM reference -
7 associated genes
No signs/symptoms info
Atypical hemolytic uremic syndrome with H factor anomaly
Acute promyelocytic leukemia

CFH
(UniProt - OMIM)
 NABP1
(UniProt - OMIM)
NPM1
(UniProt - OMIM)
NUMA1
(UniProt - OMIM)
PML
(UniProt - OMIM)
RARA
(UniProt - OMIM)
STAT5B
(UniProt - OMIM)
ZBTB16
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CFH
(0.63)
ZBTB16


Citations in the biomedical literature:


Atypical hemolytic uremic syndrome with H factor anomaly
CFH
Acute promyelocytic leukemia
NABP1 NPM1 NUMA1 PML RARA STAT5B
ZBTB16



Atypical hemolytic uremic syndrome with H factor anomaly
Acute promyelocytic leukemia

Synonym(s):
- Atypical HUS with H factor anomaly
- D-HUS with H factor anomaly
- Hemolytic-uremic syndrome without diarrhea with H factor anomaly
- aHUS with H factor anomaly
Synonym(s):
- Acute myeloblastic leukemia type 3
- Acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare renal 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:
(no data available)
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D015473
No signs/symptoms info available.