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Mazabraud syndrome
1 associated gene
5 signs/symptoms
COMMON GENES: 1
Monostotic fibrous dysplasia
1 associated gene
No signs/symptoms info
Mazabraud syndrome
Monostotic fibrous dysplasia

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

COMMON
GENES 		GNAS


Citations in the biomedical literature:


Mazabraud syndrome
GNAS
Monostotic fibrous dysplasia



Mazabraud syndrome
Monostotic fibrous dysplasia

Synonym(s):
- Myxoma with fibrous dysplasia
Synonym(s):
(no synonyms)
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
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
1 MeSH reference: D005358
Mazabraud syndrome

Very frequent
- Fibromatosis / bone fibroma
- Neoplasms / tumors

Occasional
- Anomalies of bones / skeletal anomalies
- Bone / osseous neoplasm / tumor / carcinoma / cancer
- Mutiple fractures / bone fragility


Monostotic fibrous dysplasia

(no data available)