disease has feature Chorioretinal lacunae syndromic disease Aicardi syndrome https://github.com/monarch-initiative/mondo/issues/3680 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6744 https://rarediseases.info.nih.gov/diseases/5764/aicardi-syndrome https://www.malacards.org/card/aicardi_syndrome UMLS:C0175713 DOID:8461 MEDGEN:61236 NANDO:1200562 agenesis of corpus callosum with chorioretinal abnormality Orphanet:50 AIC corpus callosum, agenesis of, with chorioretinal abnormality Aicardi’s syndrome icd11.foundation:2057245946 OMIM:304050 MESH:D058540 MONDO:0010568 corpus callosum agenesis of with chorioretinal abnormality NCIT:C35256 Aicardi syndrome, X-linked dominant MedDRA:10054935 Aicardi syndrome is a rare neurodevelopmental disorder defined by the triad of agenesis of the corpus callosum (total or partial), typical chorioretinal lacunae and infantile spasms that affect almost exclusively females. NORD:745 GARD:0005764 Aicardi syndrome SCTID:80651009 obsolete syndromic developmental defect of the eye X-linked syndromic intellectual disability disorder of development or morphogenesis neurodevelopmental disorder