ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Permanent neonatal diabetes mellitus

Familial retinoblastoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	INS	(0.65)	RB1

Citations in the biomedical literature:

Permanent neonatal diabetes mellitus		Familial retinoblastoma
	Synonym(s): - PNDM		Synonym(s): - Bilateral retinoblastoma - Hereditary retinoblastoma

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

	Classification (ICD10): - Certain conditions originating in the perinatal period -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant

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

No signs/symptoms info available.