Ghosal hematodiaphyseal dysplasia
Ghosal hematodiaphyseal dysplasia syndrome (GHDD) is a rare disorder characterized by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anemia
Press Enter · cited answer in seconds
0 sources
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's subclass of is recorded as primary bone dysplasia with increased bone density[5].
- Ghosal hematodiaphyseal dysplasia's MeSH descriptor ID is recorded as C565551[6].
- Ghosal hematodiaphyseal dysplasia's OMIM ID is recorded as 231095[7].
- Ghosal hematodiaphyseal dysplasia's DiseasesDB is recorded as 34928[8].
- Ghosal hematodiaphyseal dysplasia's KEGG ID is recorded as H00490[9].
- Ghosal hematodiaphyseal dysplasia's Orphanet ID is recorded as 1802[10].
- Ghosal hematodiaphyseal dysplasia's ICD-9-CM is recorded as 756.59[11].
- Ghosal hematodiaphyseal dysplasia's genetic association is recorded as TBXAS1[12].
- Ghosal hematodiaphyseal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1802[13].
- Ghosal hematodiaphyseal dysplasia's UMLS CUI is recorded as C1856465[14].
- Ghosal hematodiaphyseal dysplasia's GARD rare disease ID is recorded as 10297[15].
- Ghosal hematodiaphyseal dysplasia's Mondo ID is recorded as MONDO_0009274[16].
- Ghosal hematodiaphyseal dysplasia's Genetics Home Reference Conditions ID is recorded as ghosal-hematodiaphyseal-dysplasia[17].
- Ghosal hematodiaphyseal dysplasia's UniProt disease ID is recorded as DI-01657[18].