ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

2 OMIM references -
2 associated genes
No signs/symptoms info

Autosomal recessive hypophosphatemic rickets

Generalized arterial calcification of infancy

DMP1	(UniProt - OMIM)		ABCC6	(UniProt - OMIM)
ENPP1	(UniProt - OMIM)		ENPP1	(UniProt - OMIM)

Citations in the biomedical literature:

Autosomal recessive hypophosphatemic rickets		Generalized arterial calcification of infancy
	Synonym(s): - ARHR		Synonym(s): - Idiopathic infantile arterial calcification - Idiopathic obliterative arteriopathy - Infantile arteriosclerosis - Occlusive infantile arteriopathy

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C537440

No signs/symptoms info available.