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11 Jul 2019	Intellectual disability v2.951	NEXMIF	Rebecca Foulger Publications for gene: NEXMIF were set to
11 Jul 2019	Intellectual disability v2.950	NEXMIF	Rebecca Foulger Added comment: Comment on mode of inheritance: Changed MOI from XLR to XLD to match the XLD recorded for 'Mental retardation, X-linked 98' in OMIM (MIM:300912) and Gene2Phenotype, which records X-linked dominant inheritance for 'Intellectual disability and epilepsy' in addition to hemizgyous inheritance for 'KIAA2022'. An XLD inheritance is supported by PMID:27358180 which reports 14 female patients who carry a heterozygous de novo NEXMIF (KIAA2022) variant and share a phenotype characterised by intellectual disability and epilepsy.
11 Jul 2019	Intellectual disability v2.950	NEXMIF	Rebecca Foulger Mode of inheritance for gene: NEXMIF was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
29 Sep 2018	Intellectual disability v2.468	NEXMIF	Louise Daugherty Source Victorian Clinical Genetics Services was added to NEXMIF.