ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Infant acute respiratory distress syndrome

X-linked intellectual deficit, Porteous type

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


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

Citations in the biomedical literature:

Infant acute respiratory distress syndrome		X-linked intellectual deficit, Porteous type
	Synonym(s): - Hyaline membrane disease - Infant ARDS - Infant respiratory distress syndrome - Neonatal respiratory distress syndrome		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Certain conditions originating in the perinatal period -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: sporadic		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.