has material basis in germline mutation in disease arises from structure disease arises from alteration in structure FRAXD Xq27.2 (Human) hereditary disease chromosomal disorder FRAXD syndrome https://github.com/monarch-initiative/mondo/issues/7700 https://rarediseases.info.nih.gov/diseases/2377/fraxd Reason of obsoletion: out of scope - MONDO:excludeHistoricalDisease. Term to consider: - MONDO:0023099 FRAXD 2024-09-01