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Monostotic fibrous dysplasia
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Mazabraud syndrome
McCune-Albright syndrome
Polyostotic fibrous dysplasia
Progressive osseous heteroplasia
Pseudohypoparathyroidism type 1A
Pseudohypoparathyroidism type 1B
Pseudohypoparathyroidism type 1C
Pseudopseudohypoparathyroidism
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D005358
Gene symbol UniProt reference OMIM reference
GNAS P63092139320
No signs/symptoms info available.