has material basis in germline mutation in disease has feature TBXAS1 Increased bone mineral density ghosal hematodiaphyseal dysplasia https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/6877 https://rarediseases.info.nih.gov/diseases/10297/ghosal-hematodiaphyseal-dysplasia-syndrome https://www.malacards.org/card/ghosal_hematodiaphyseal_dysplasia GHDD Ghosal hematodiaphyseal dysplasia syndrome (GHDD) is a rare disorder characterized by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anemia. Ghosal hematodiaphyseal dysplasia syndrome Orphanet:1802 diaphyseal dysplasia-anemia syndrome Ghosal syndrome ICD9:756.59 GARD:0010297 MONDO:0009274 UMLS:C1856465 ghosal hematodiaphyseal dysplasia MESH:C565551 OMIM:231095 MEDGEN:344739 DOID:0112251 SCTID:389214003 skeletal dysplasia obsolete primary bone dysplasia with increased bone density