ODCs

Click node...

2 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

5 OMIM references -
3 associated genes
No signs/symptoms info

Familial isolated hyperparathyroidism

Periventricular nodular heterotopia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CDC73	(0.63)	ARFGEF2

Citations in the biomedical literature:

Familial isolated hyperparathyroidism		Periventricular nodular heterotopia
	Synonym(s): - FIHPT		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 5 OMIM references - 1 MeSH reference: D054091

No signs/symptoms info available.