has material basis in germline mutation in ANO5 gnathodiaphyseal dysplasia https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/gnathodiaphyseal_dysplasia MEDGEN:331575 Orphanet:53697 icd11.foundation:1984860886 Gnathodiaphyseal dysplasia (GDD) is a bone dysplasia characterized by bone fragility, frequent bone fractures at a young age, cemento-osseous lesions of the jaw bones, bowing of tubular bones (tibia and fibula) and diaphyseal sclerosis of long bones associated with generalized osteopenia. GD follows an autosomal dominant mode of transmission. gnathodiaphyseal dysplasia MESH:C536039 SCTID:715568002 GDD UMLS:C1833736 Levin syndrome 2 osteogenesis imperfecta Levin type GARD:0008698 OMIM:166260 MONDO:0008151 DOID:0111533 obsolete primary bone dysplasia with decreased bone density obsolete primary bone dysplasia with disorganized development of skeletal components osteogenesis imperfecta and a reduction of bone mineral density.