Cytoscape Web
Click node...

Congenital mesoblastic nephroma
2 associated genes
42 connected diseases
No signs/symptoms info
Disease Type of connection
Chronic myelomonocytic leukemia
Precursor B-cell acute lymphoblastic leukemia
Distal 22q11.2 microdeletion syndrome
Amyotrophic lateral sclerosis
Ewing sarcoma
Extraskeletal Ewing sarcoma
Isolated delta-storage pool disease
Paris-Trousseau thrombocytopenia
Peripheral primitive neuroectodermal tumor
Peters anomaly
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Anophthalmia / microphthalmia - esophageal atresia
Bilateral striopallidodentate calcinosis
Burkitt lymphoma
Colobomatous microphthalmia
Distal myopathy with posterior leg and anterior hand involvement
Herpetic encephalitis
Idiopathic hypereosinophilic syndrome
Infantile myofibromatosis
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Isolated anophthalmia - microphthalmia
Muscle filaminopathy
Myeloid neoplasm associated with PDGFRB rearrangement
Precursor T-cell acute lymphoblastic leukemia
Septo-optic dysplasia
Unclassified chronic myeloproliferative disease
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Pediatric systemic lupus erythematosus
(no synonyms)

Classification (Orphanet):
(no data available)
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D018201

Gene symbol UniProt reference OMIM reference
ETV6 P41212600618
NTRK3 Q16288191316
No signs/symptoms info available.