disease has feature Narrow chest Severe short stature osteochondrodysplasia achondrogenesis https://rarediseases.info.nih.gov/diseases/2882/achondrogenesis https://www.malacards.org/card/achondrogenesis UMLS:C0001079 MedDRA:10066122 MEDGEN:84 GARD:0002882 OMIMPS:200600 NORD:710 icd11.foundation:103965243 MONDO:0019648 MESH:C579878 Achondrogenesis describes a rare group of lethal skeletal dysplasias characterized by an endochondral ossification deficiency that leads to dwarfism with extreme micromelia, a small thorax, a prominent abdomen, anasarca and polyhydramnios. There are three types of achondrogenesis that exist and that differ clinically, radiologically, histologically and genetically: achondrogensis type 1a, type 1b and type 2. Orphanet:932 SCTID:2391001 DOID:0080043 NCIT:C84527 ICD10CM:Q77.0 spondylodysplastic dysplasia