syndromic intellectual disability syndromic disease multiple congenital anomalies/dysmorphic syndrome-intellectual disability microcephaly-microcornea syndrome, Seemanova type https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/6744 https://github.com/monarch-initiative/mondo/issues/6745 https://rarediseases.info.nih.gov/diseases/3627/microcephaly-microcornea-syndrome-seemanova-type https://www.malacards.org/card/microcephaly_microcornea_syndrome_seemanova_type_2 Seemanova Lesny syndrome MEDGEN:419433 Seemanova-Lesny syndrome Microcephaly-microcornea syndrome, Seemanova type is characterized by microcephaly and brachycephaly, eye anomalies (microphthalmia, microcornea, congenital cataract), hypogenitalism, severe intellectual deficit, growth retardation and progressive spasticity. It has been described in two patients (a male and his sister's son). Both patients also presented with facial dysmorphism, including upslanting palpebral fissures, epicanthal folds, highly arched palate, microstomia, and retrognathia. This syndrome is transmitted as an X-linked trait. icd11.foundation:1197077842 MESH:C537539 SCTID:715464002 UMLS:C2931524 Orphanet:2528 GARD:0003627 microcephaly microcornea syndrome Seemanova type MONDO:0016760 X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation disorder of visual system