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

PQBP1
(UniProt - OMIM)
 SFTPC
(UniProt - OMIM)

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


Citations in the biomedical literature:


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



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

Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare respiratory disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.