hereditary disease splenogonadal fusion-limb defects-micrognathia syndrome https://github.com/monarch-initiative/mondo/issues/6877 https://www.malacards.org/card/splenogonadal_fusion_with_limb_defects_and_micrognathia Orphanet:2063 Splenogonadal fusion-limb defects-micrognatia syndrome is a rare dysostosis syndrome characterized by abnormal fusion of the spleen with the gonad (or more rarely with remnants of the mesonephros), limb abnormalities (consisting of amelia or severe reduction defects leading to upper and/or lower rudimentary limbs) and orofacial abnormalities such as cleft palate, bifid uvula, microglossia and mandibular hypoplasia. It could also be associated with other malformations such as cryptorchidism, anal stenosis/atresia, hypoplastic lungs and cardiac malformations. GARD:0004963 MONDO:0008460 UMLS:C1866745 splenogonadal fusion limb defects micrognatia SGFLD syndrome splenogonadal fusion limb defects syndrome OMIM:183300 MESH:C537318 SCTID:726724005 MEDGEN:401073 dysostosis congenital limb malformation