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5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
5 associated genes
No signs/symptoms info
Congenital pulmonary alveolar proteinosis
Juvenile myelomonocytic leukemia

ABCA3 CBL
CSF2RA KRAS
CSF2RB NF1
SFTPB NRAS
SFTPC PTPN11


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CSF2RB
(0.89)
PTPN11



Citations in the biomedical literature:


Congenital pulmonary alveolar proteinosis
ABCA3 CSF2RA CSF2RB SFTPB SFTPC
Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11



Congenital pulmonary alveolar proteinosis
Juvenile myelomonocytic leukemia

Synonym(s):
- Congenital PAP

Synonym(s):
- Juvenile chronic myelomonocytic leukemia

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

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

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
5 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D054429

No signs/symptoms info available.