ODCs

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

COMMON GENES: 1

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

Osteopetrosis - hypogammaglobulinemia

Familial expansile osteolysis

Citations in the biomedical literature:

Osteopetrosis - hypogammaglobulinemia		Familial expansile osteolysis
	Synonym(s): - Autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia - Autosomal recessive osteopetrosis type 7		Synonym(s): - Hereditary expansile polyostotic osteolytic dysplasia - McCabe's disease

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare immune disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		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		External references: 1 OMIM reference - 1 MeSH reference: C536335

No signs/symptoms info available.