ODCs

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

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Pseudohypoparathyroidism type 1B

Monostotic fibrous dysplasia

GNAS	(UniProt - OMIM)		GNAS	(UniProt - OMIM)
STX16	(UniProt - OMIM)

Citations in the biomedical literature:

Pseudohypoparathyroidism type 1B		Monostotic fibrous dysplasia

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

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

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C548075		External references: No OMIM references 1 MeSH reference: D005358

No signs/symptoms info available.