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Pseudohypoparathyroidism type 1B
1 OMIM reference -
2 associated genes
9 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 1A
Pseudohypoparathyroidism type 1C
Pseudopseudohypoparathyroidism
Recurrent infections-myelofibrosis-nephromegaly syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C548075
Gene symbol UniProt reference OMIM reference
GNAS P63092139320
STX16 O14662603666
No signs/symptoms info available.