has material basis in germline mutation in disease has feature KIF11 autosomal dominant disease microcephaly syndromic disease microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability https://github.com/monarch-initiative/mondo/issues/6878 https://github.com/monarch-initiative/mondo/issues/9498 https://www.malacards.org/card/microcephaly_with_or_without_chorioretinopathy_lymphedema_or_impaired_intellectual_development MLCRD syndrome MONDO:0007918 GARD:0003622 microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability A microcephaly caused by a mutation in KIF11 gene and follows autosomal dominant inheritance. It is characterized by variable expression of microcephaly, ocular disorders including chorioretinopathy, congenital lymphedema of the lower limbs, and mild to moderate intellectual disability. UMLS:C1835265 KIF11-associated disorder MLCRD microcephaly, lymphedema, chorioretinal dysplasia syndrome MCLMR KIF11 disease MESH:C537711 OMIM:152950 microcephaly with or without chorioretinopathy, lymphedema, or mental retardation microcephaly and chorioretinopathy with or without mental retardation, autosomal dominant lymphedema, microcephaly and chorioretinopathy syndrome MEDGEN:320559 Orphanet:2526 DOID:0060349 inherited retinal dystrophy lymphatic malformation neurovascular disorder Mendelian neurodevelopmental disorder