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5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
5 associated genes
No signs/symptoms info
Congenital pulmonary alveolar proteinosis
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

ABCA3 CEBPA
CSF2RA FLT3
CSF2RB KIT
SFTPB RUNX1
SFTPC RUNX1T1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CSF2RA
CSF2RB
(0.52)
(0.52)
KIT
KIT



Citations in the biomedical literature:


Congenital pulmonary alveolar proteinosis
ABCA3 CSF2RA CSF2RB SFTPB SFTPC
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
CEBPA FLT3 KIT RUNX1 RUNX1T1



Congenital pulmonary alveolar proteinosis
Acute myeloid leukemia with t(8;21)(q22;q22) translocation

Synonym(s):
- Congenital PAP

Synonym(s):
(no synonyms)

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:
No OMIM references
No MeSH references

No signs/symptoms info available.