has material basis in germline mutation in FGFR3 Muenke syndrome https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/9798 https://rarediseases.info.nih.gov/diseases/2479/glass-chapman-hockley-syndrome https://rarediseases.info.nih.gov/diseases/7097/muenke-syndrome https://www.malacards.org/card/muenke_syndrome NCIT:C84904 Orphanet:53271 craniosynostosis with facial dysmorphism and brachydactyly syndrome Muenke syndrome syndrome of coronal craniosynostosis FGFR3-related craniosynostosis Orphanet:1535 GARD:0007097 craniosynostosis-dysmorphism-brachydactyly syndrome OMIM:602849 MONDO:0011274 MNKES Muenke syndrome is a syndromic craniosynostosis with significant phenotypic variability, usually characterized by coronal synostosis, midfacial retrusion, strabismus, hearing loss and developmental delay. MEDGEN:355217 craniosynostosis brachydactyly craniosynostosis - dysmorphism - brachydactyly MESH:C537369 icd11.foundation:1860572017 glass-chapman-hockley syndrome SCTID:440350001 SCTID:720814001 UMLS:C1864436 DOID:0060703 syndromic craniosynostosis