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1 OMIM reference -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pseudohypoparathyroidism type 1B
Pseudopseudohypoparathyroidism

GNAS GNAS
STX16


COMMON
GENES
GNAS



Citations in the biomedical literature:


Pseudohypoparathyroidism type 1B
GNAS STX16
Pseudopseudohypoparathyroidism



Pseudohypoparathyroidism type 1B
Pseudopseudohypoparathyroidism

Synonym(s):
(no synonyms)

Synonym(s):
- AHO - PPHP
- Albright hereditary osteodystrophy - PPHP

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare renal disease
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 -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C548075
External references:
1 OMIM reference -
1 MeSH reference: D011556

No signs/symptoms info available.