ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Aplasia of lacrimal and salivary glands

FGFR2-related bent bone dysplasia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FGF10	(0.9)	FGFR2

Citations in the biomedical literature:

Aplasia of lacrimal and salivary glands		FGFR2-related bent bone dysplasia
	Synonym(s): - ALSG - Congenital absence of lacrimal puncta and salivary glands		Synonym(s): - Perinatal lethal bent bone dysplasia

	Classification (Orphanet): - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.