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Juvenile myelomonocytic leukemia
1 OMIM reference -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Succinyl-CoA:3-ketoacid CoA transferase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Juvenile myelomonocytic leukemia
Succinyl-CoA:3-ketoacid CoA transferase deficiency

CBL
(UniProt - OMIM)
 OXCT1
(UniProt - OMIM)
KRAS
(UniProt - OMIM)
NF1
(UniProt - OMIM)
NRAS
(UniProt - OMIM)
PTPN11
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
PTPN11
(0.63)
OXCT1


Citations in the biomedical literature:


Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11
Succinyl-CoA:3-ketoacid CoA transferase deficiency
OXCT1



Juvenile myelomonocytic leukemia
Succinyl-CoA:3-ketoacid CoA transferase deficiency

Synonym(s):
- Juvenile chronic myelomonocytic leukemia
Synonym(s):
- OXCT1 deficiency
- SCOT deficiency
- Succinyl-CoA acetoacetate transferase deficiency
- Succinyl-CoA:3-oxoacid CoA transferase deficiency
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
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:
1 OMIM reference -
1 MeSH reference: D054429
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.