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Pseudohypoparathyroidism type 1A
1 OMIM reference -
1 associated gene
8 connected diseases
No signs/symptoms info
Disease Type of connection
Mazabraud syndrome
McCune-Albright syndrome
Monostotic fibrous dysplasia
Polyostotic fibrous dysplasia
Progressive osseous heteroplasia
Pseudohypoparathyroidism type 1B
Pseudohypoparathyroidism type 1C
Pseudopseudohypoparathyroidism
Synonym(s):
- AHO - PHP Ia
- Albright hereditary osteodystrophy - PHP Ia
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare eye disease
- Rare genetic disease
- Rare renal disease
- Rare skin disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
GNAS P63092139320
No signs/symptoms info available.