syndromic disease familial osteodysplasia, Anderson type https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6876 https://github.com/monarch-initiative/mondo/issues/6877 https://rarediseases.info.nih.gov/diseases/4136/osteodysplasia-familial-anderson-type https://www.malacards.org/card/osteodysplasia_familial_anderson_type_2 MEDGEN:337990 OMIM:259250 osteodysplasia familial Anderson type osteodysplasia, familial, Anderson type UMLS:C1850186 Orphanet:2769 Familial osteodysplasia, Anderson type is a rare, genetic dysostosis disorder characterized by craniofacial bone abnormalities (i.e. midface hypoplasia, broad, flat nasal bridge, narrow, thin prognathic mandible with pointed chin, malocclusion, partial dental agenesis) associated with additional osseous anomalies, including scoliosis, calvarial thinning, pointed spinous processes, clinodactyly and abnormal phalanges. Elevated erythrocyte sedimentation rate, hyperuricemia and hypertension have also been reported. There have been no further descriptions in the literature since 1982. MONDO:0009801 GARD:0004136 icd11.foundation:107132680 MESH:C564923 skeletal dysplasia disorder of development or morphogenesis