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Monostotic fibrous dysplasia

1 associated gene
No signs/symptoms info

COMMON GENES: 1

Progressive osseous heteroplasia

1 OMIM reference -
1 associated gene
14 signs/symptoms

Monostotic fibrous dysplasia

Progressive osseous heteroplasia

GNAS

(UniProt - OMIM)

GNAS

(UniProt - OMIM)


COMMON GENES	GNAS

Citations in the biomedical literature:

Monostotic fibrous dysplasia		Progressive osseous heteroplasia
	Synonym(s): (no synonyms)		Synonym(s): - Familial ectopic ossification

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -

	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

Progressive osseous heteroplasia
	Very frequent - Anomalies of bones / skeletal anomalies - Autosomal dominant inheritance - Bone pain - Bone tumefaction / swelling - Restricted joint mobility / joint stiffness / ankylosis - Subcutaneous nodules / lipomas / tumefaction / swelling Frequent - Muscle ossification Occasional - Capillary hemangioma / nevus / naevus flammeus / port-wine stain - Follicular / erythematous / edematous papules / milium - Macules - Osteoarthritis - Parathyroids anomalies - Sarcoma - Short hand / brachydactyly
Monostotic fibrous dysplasia
(no data available)