holoprosencephaly-craniosynostosis syndrome https://github.com/monarch-initiative/mondo/issues/6751 https://www.malacards.org/card/holoprosencephaly_semilobar_with_craniosynostosis SCTID:715434005 Semilobar holoprosencephaly and primary craniosynostosis Holoprosencephaly-craniosynostosis syndrome is a rare developmental defect during embryogenesis syndrome characterized by the association of primary craniosynostosis (usually involving the coronal and metopic sutures) with holoprosencephaly (ranging from alobar to, most commonly, semilobar) and various skeletal anomalies (typically, hand and feet anomalies including fifth digit clinodactyly, hypoplastic phalanges and cone-shaped epiphyses, small vertebral bodies, scoliosis, coxa valga and/or flexion deformities of hips). Craniofacial asymmetry, microcephaly, brachy/plagiocephaly, short stature and psychomotor delay are additional common features. Orphanet:2163 holoprosencephaly craniosynostosis UMLS:C1832424 camera Lituania Cohen syndrome MESH:C537684 MEDGEN:330464 Camero-Lituania-Cohen syndrome Genoa syndrome GARD:0002454 MONDO:0011059 OMIM:601370 syndromic craniosynostosis