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Congenital pulmonary alveolar proteinosis
5 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
1 associated gene
4 signs/symptoms
Congenital pulmonary alveolar proteinosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

ABCA3
(UniProt - OMIM)
 KIT
(UniProt - OMIM)
CSF2RA
(UniProt - OMIM)
CSF2RB
(UniProt - OMIM)
SFTPB
(UniProt - OMIM)
SFTPC
(UniProt - OMIM)

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
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
KIT



Congenital pulmonary alveolar proteinosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

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:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
5 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease

Very frequent
- Acute leukemia
- Eosinophils anomalies / hypereosinophilia
- Mastocytosis
- Myeloproliferative syndrome / chronic leukemia



Congenital pulmonary alveolar proteinosis

(no data available)