has material basis in germline mutation in SCYL2 arthrogryposis multiplex congenita arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum https://www.malacards.org/card/arthrogryposis_multiplex_congenita_4 https://www.malacards.org/card/arthrogryposis_multiplex_congenita_4_neurogenic_with_agenesis_of_the_corpus_callosum OMIM:618766 MONDO:0032903 Zain Syndrome DOID:0080980 AMCNACC GARD:0025768 UMLS:C5231494 arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum MEDGEN:1684706