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

Polyostotic fibrous dysplasia

Pseudopseudohypoparathyroidism

GNAS

Citations in the biomedical literature:

Polyostotic fibrous dysplasia		Pseudopseudohypoparathyroidism
	Synonym(s): - Jaffe-Lichtenstein disease		Synonym(s): - AHO - PPHP - Albright hereditary osteodystrophy - PPHP

	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: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: unknown		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: D005359		External references: 1 OMIM reference - 1 MeSH reference: D011556

No signs/symptoms info available.