ODCs

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

COMMON GENES: 1

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

Familial hypocalciuric hypercalcemia type 1

Familial isolated hypoparathyroidism due to impaired PTH secretion

CASR	(UniProt - OMIM)		CASR	(UniProt - OMIM)
			PTH	(UniProt - OMIM)

Citations in the biomedical literature:

Familial hypocalciuric hypercalcemia type 1		Familial isolated hypoparathyroidism due to impaired PTH secretion
	Synonym(s): - FHH type 1		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	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: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C537145		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.