ZFIN Human Disease: non-syndromic X-linked intellectual disability 41

OBO ID: DOID:0112058

Term Name:	non-syndromic X-linked intellectual disability 41		Search Ontology:
Synonyms:	MRX41 MRX48 X-linked mental retardation 41 X-linked mental retardation 48
Definition:	A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in heterozygous mutation in the GDI1 gene on chromosome Xq28. (3)
References:	OMIM:300849
Ontology:	Human Disease ( DOID:0112058 )

Relationships

is a type of:	non-syndromic X-linked intellectual disability X-linked dominant disease non-syndromic X-linked intellectual disability X-linked dominant disease Show first 5 Terms

OTHER non-syndromic X-linked intellectual disability 41 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GDI1	gdi1	Intellectual developmental disorder, X-linked 41	300849

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None