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Familial isolated hyperparathyroidism

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

PROTEIN INTERACTIONS: 1

Frasier syndrome

1 OMIM reference -
1 associated gene
7 signs/symptoms

Familial isolated hyperparathyroidism

Frasier syndrome

CDC73	(UniProt - OMIM)		WT1	(UniProt - OMIM)
MEN1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MEN1	(0.63)	WT1

Citations in the biomedical literature:

Familial isolated hyperparathyroidism		Frasier syndrome
	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 endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare oncologic disease - Rare renal disease - Rare urogenital disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the genitourinary system -

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

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D052159

Frasier syndrome
	Very frequent - Late puberty / hypogonadism / hypogenitalism - Male pseudohermaphrodism / lack of virilisation - Primary amenorrhea Frequent - Nephrotic syndrome - Proteinuria - Renal failure - Renal glomerular defect / glomerulopathy
Familial isolated hyperparathyroidism
(no data available)