autosomal dominant intellectual developmental disorder 39

Summary
Synonym
  • MRD39
  • autosomal dominant mental retardation 39
  • autosomal dominant non-syndromic intellectual disability 39
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3.
Super Class
autosomal dominant intellectual developmental disorder
Disease Ontology
DOID:0070069
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
17933 Myt1l myelin transcription factor 1-like

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024