ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1

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

Prenatal benign hypophosphatasia

Perinatal lethal hypophosphatasia

ALPL

Citations in the biomedical literature:

Prenatal benign hypophosphatasia		Perinatal lethal hypophosphatasia
	Synonym(s): - Prenatal benign Rathburn disease - Prenatal benign phosphoethanolaminuria		Synonym(s): - Perinatal lethal Rathburn disease - Perinatal lethal phosphoethanolaminuria

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

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

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

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

No signs/symptoms info available.