has characteristic has characteristic schizencephaly familial schizencephaly https://github.com/monarch-initiative/mondo/issues/6740 https://github.com/monarch-initiative/mondo/issues/6882 Orphanet:481986 familial schizencephaly MEDGEN:419186 GARD:0017876 An instance of schizencephaly that is caused by an inherited modification of the individual's genome. UMLS:C2931870 This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'cardiovascular disorder' (MONDO:0004995) ontology branch (https://orcid.org/0000-0001-9310-0163, https://orcid.org/0000-0001-6718-3559) hereditary schizencephaly MESH:C538514 MONDO:0018829 inherited hereditary neurological disease COL4A1-related disorder