has material basis in germline mutation in COG1 syndromic disease congenital disorder of glycosylation type II COG1-congenital disorder of glycosylation https://github.com/monarch-initiative/mondo/issues/6751 https://www.malacards.org/card/congenital_disorder_of_glycosylation_type_iig Cdgii/Cog1 Cerebrocostomandibular-like syndrome COG1-CDG MEDGEN:443957 congenital disorder of glycosylation type IIg CDG IIg CDG syndrome type IIg MONDO:0012637 UMLS:C2931011 MESH:C535756 GARD:0010226 Orphanet:263508 OMIM:611209 congenital disorder of glycosylation type 2g CDG-IIg SCTID:718750004 COG1-CDG is an extremely rare form of CDG syndrome characterized clinically in the few cases reported to date by variable signs including microcephaly, growth retardation, psychomotor retardation and facial dysmorphism. congenital disorder of glycosylation, type IIg COG1-congenital disorder of glycosylation COG1-CDG (CDG-IIg) DOID:0070259 CDG2G CDG 2G carbohydrate deficient glycoprotein syndrome type IIg developmental anomaly of metabolic origin defect in conserved oligomeric Golgi complex cardiogenetic disease