ZFIN Human Disease: non-syndromic X-linked intellectual disability 19

OBO ID: DOID:0112019

Term Name:	non-syndromic X-linked intellectual disability 19		Search Ontology:
Synonyms:	MRX19 X-linked mental retardation 19
Definition:	A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability that has_material_basis_in hemizygous or heterozygous mutation in the RPS6KA3 gene on chromosome Xp22.12. https://pubmed.ncbi.nlm.nih.gov/17100996/
References:	OMIM:300844
Ontology:	Human Disease ( DOID:0112019 )

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 19 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RPS6KA3	rps6ka3a rps6ka3b	Intellectual developmental disorder, X-linked 19	300844

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None