ODCs

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

PROTEIN INTERACTIONS: 1

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

Obesity due to pro-opiomelanocortin deficiency

Aplasia of lacrimal and salivary glands


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	POMC	(0.52)	FGF10

Citations in the biomedical literature:

Obesity due to pro-opiomelanocortin deficiency		Aplasia of lacrimal and salivary glands
	Synonym(s): - POMC deficiency		Synonym(s): - ALSG - Congenital absence of lacrimal puncta and salivary glands

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.