ZFIN Human Disease: neurodevelopmental disorder with involuntary movements

OBO ID: DOID:0112276

Term Name:	neurodevelopmental disorder with involuntary movements		Search Ontology:
Synonyms:	NEDIM
Definition:	A movement disease characterized by delayed psychomotor development and infantile or childhood onset of hyperkinetic involuntary movements, including chorea and athetosis that has_material_basis_in heterozygous mutation of the GNAO1 gene on chromosome 16q13. (2)
References:	OMIM:617493
Ontology:	Human Disease ( DOID:0112276 )

Relationships

is a type of:	autosomal dominant disease movement disease autosomal dominant disease movement disease Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GNAO1	gnao1b gnao1a	Neurodevelopmental disorder with involuntary movements	617493

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None