ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Pseudohypoparathyroidism type 1A

Pseudohypoparathyroidism type 1B

GNAS	(UniProt - OMIM)		GNAS	(UniProt - OMIM)
			STX16	(UniProt - OMIM)

Citations in the biomedical literature:

Pseudohypoparathyroidism type 1A		Pseudohypoparathyroidism type 1B
	Synonym(s): - AHO - PHP Ia - Albright hereditary osteodystrophy - PHP Ia		Synonym(s): (no synonyms)

	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 (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare renal disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C548075

No signs/symptoms info available.