Disease #05920 (NEDMIAL (neurodevelopmental disorder with severe motor impairment and absent language (NEDMIAL)), OMIM:617804)

Official abbreviation NEDMIAL
Name neurodevelopmental disorder with severe motor impairment and absent language (NEDMIAL)
OMIM ID 617804
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene DHX30
Associated tissues -
Disease features -
Remarks -