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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Chronic respiratory distress with surfactant metabolism deficiency
X-linked intellectual deficit, Porteous type

SFTPC PQBP1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SFTPC
(0.56)
PQBP1



Citations in the biomedical literature:


Chronic respiratory distress with surfactant metabolism deficiency
SFTPC
X-linked intellectual deficit, Porteous type
PQBP1



Chronic respiratory distress with surfactant metabolism deficiency
X-linked intellectual deficit, Porteous type

Classification (Orphanet):
- Rare genetic disease
- Rare respiratory disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.