ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1

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

Monostotic fibrous dysplasia

Pseudohypoparathyroidism type 1A

GNAS

Citations in the biomedical literature:

Monostotic fibrous dysplasia		Pseudohypoparathyroidism type 1A
	Synonym(s): (no synonyms)		Synonym(s): - AHO - PHP Ia - Albright hereditary osteodystrophy - PHP Ia

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare eye disease - Rare genetic disease - Rare renal disease - Rare skin disease

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

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

	External references: No OMIM references 1 MeSH reference: D005358		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.