Ghosal hematodiaphyseal dysplasia
Ghosal hematodiaphyseal dysplasia syndrome (GHDD) is a rare disorder characterized by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anemia
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Ghosal hematodiaphyseal dysplasia
Summary
Ghosal hematodiaphyseal dysplasia is a developmental defect during embryogenesis[1].
Key Facts
- Ghosal hematodiaphyseal dysplasia's instance of is recorded as developmental defect during embryogenesis[2].
- Ghosal hematodiaphyseal dysplasia's instance of is recorded as rare disease[3].
- Ghosal hematodiaphyseal dysplasia's instance of is recorded as class of disease[4].
- Ghosal hematodiaphyseal dysplasia is a type of primary bone dysplasia with increased bone density[5].
- Ghosal hematodiaphyseal dysplasia's ICD-9-CM is recorded as 756.59[6].
- Ghosal hematodiaphyseal dysplasia's genetic association is recorded as TBXAS1[7].
- Ghosal hematodiaphyseal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1802[8].