Cytoscape Web
Click node...

Mazabraud syndrome
1 associated gene
8 connected diseases
5 signs/symptoms
Disease Type of connection
McCune-Albright syndrome
Monostotic fibrous dysplasia
Polyostotic fibrous dysplasia
Progressive osseous heteroplasia
Pseudohypoparathyroidism type 1A
Pseudohypoparathyroidism type 1B
Pseudohypoparathyroidism type 1C
Pseudopseudohypoparathyroidism
Synonym(s):
- Myxoma with fibrous dysplasia
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
GNAS P63092139320
Very frequent
- Fibromatosis / bone fibroma
- Neoplasms / tumors

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