Cytoscape Web
Click node...


2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
12 signs/symptoms
Acute myeloblastic leukemia without maturation
Pierson syndrome

FLT3 LAMB2
NPM1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NPM1
(0.63)
LAMB2



Citations in the biomedical literature:


Acute myeloblastic leukemia without maturation
FLT3 NPM1
Pierson syndrome
LAMB2



Acute myeloblastic leukemia without maturation
Pierson syndrome

Synonym(s):
- Acute myeloblastic leukemia type 1

Synonym(s):
- Microcoria - congenital nephrosis

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the genitourinary system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537185

Pierson syndrome

Very frequent
- Autosomal recessive inheritance
- Cataract / lens opacification
- Chronic arterial hypertension
- EEG anomalies
- Hematuria / microhematuria
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Hypotonia
- Movement disorder
- Nephrotic syndrome
- Nystagmus
- Proteinuria

Frequent
- Micropenis / small penis / agenesis



Acute myeloblastic leukemia without maturation

(no data available)