Polyostotic osteolytic dysplasia, hereditary expansile
human disease
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Polyostotic osteolytic dysplasia, hereditary expansile
Summary
Polyostotic osteolytic dysplasia, hereditary expansile is a developmental defect during embryogenesis[1].
Key Facts
- Polyostotic osteolytic dysplasia, hereditary expansile's instance of is recorded as developmental defect during embryogenesis[2].
- Polyostotic osteolytic dysplasia, hereditary expansile's instance of is recorded as rare disease[3].
- Polyostotic osteolytic dysplasia, hereditary expansile's instance of is recorded as class of disease[4].
- Polyostotic osteolytic dysplasia, hereditary expansile is a type of osteolysis[5].
- Polyostotic osteolytic dysplasia, hereditary expansile is a type of primary osteolysis[6].
- Polyostotic osteolytic dysplasia, hereditary expansile is a type of autosomal dominant disease[7].
- Polyostotic osteolytic dysplasia, hereditary expansile is a type of bone remodeling disease[8].
- Polyostotic osteolytic dysplasia, hereditary expansile's ICD-9-CM is recorded as 756.9[9].
- Polyostotic osteolytic dysplasia, hereditary expansile's genetic association is recorded as TNFRSF11A[10].
- Polyostotic osteolytic dysplasia, hereditary expansile's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85195[11].
- Polyostotic osteolytic dysplasia, hereditary expansile's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111542[12].
- Polyostotic osteolytic dysplasia, hereditary expansile's exact match is recorded as http://identifiers.org/doid/DOID:0111542[13].