disease arises from structure disease arises from alteration in structure 10q24 (Human) split hand-foot malformation 3 https://github.com/monarch-initiative/mondo/issues/3492 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4948 https://rarediseases.info.nih.gov/diseases/3252/limb-deficiencies-distal-with-micrognathia https://www.malacards.org/card/split_hand_foot_malformation_3 NCIT:C75121 SCTID:722429003 Buttiens Fryns syndrome DOID:0090025 MESH:C565437 MEDGEN:325070 10q24 microduplication syndrome split hand-foot malformation type 3 Orphanet:1307 split-hand/foot malformation 3 The distal limb deficiencies-micrognathia syndrome is characterized by the combination of symmetric severe distal limb reduction deficiencies affecting all four limbs (oligodactyly), microretrognathia, and microstomia with or without cleft palate. UMLS:C1838652 chromosome 10q24 duplication syndrome limb deficiencies distal with micrognathia split-hand/foot malformation 3, gene duplication syndrome split-hand/foot malformation type 3 OMIM:246560 Buttiens-Fryns syndrome GARD:0003252 MONDO:0009525 SHFM3 split hand-foot malformation 3 multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome split hand-foot malformation partial duplication of the long arm of chromosome 10