Hunter-McAlpine craniosynostosis https://github.com/monarch-initiative/mondo/issues/6751 https://www.malacards.org/card/hunter_mcalpine_craniosynostosis_syndrome OMIM:601379 UMLS:C1832408 Orphanet:97340 MESH:C536072 Hunter-McAlpine syndrome Hunter-McAlpine craniosynostosis is characterized by craniosynostosis, intellectual deficit, short stature, facial dysmorphism (oval face with almond-shaped palpebral fissures, droopy eyelids and a small nose) and minor distal anomalies. It has been described in 10 patients. Transmission is autosomal dominant and the syndrome is associated with partial duplication of the long arm of chromosome 5 (5q35-5qter). icd11.foundation:1445975694 MEDGEN:321949 GARD:0002754 craniosynostosis, mental deficiency, almond-shaped palpebral fissures, downturned mouth, mild acral-skeletal anomalies, and short stature SCTID:721227001 MONDO:0011065 syndromic craniosynostosis