ODCs

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

PROTEIN INTERACTIONS: 1

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

Familial hypocalciuric hypercalcemia type 2

Male infertility with normal virilization due to meiosis defect


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GNA11	(0.72)	CFTR

Citations in the biomedical literature:

Familial hypocalciuric hypercalcemia type 2		Male infertility with normal virilization due to meiosis defect
	Synonym(s): - FHH type 2		Synonym(s): - Azoospermia due to maturation arrest - Azoospermia due to meiosis defect - Male infertility with normal virilization due to maturation arrest

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C537146		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.