ZFIN Human Disease: non-syndromic X-linked intellectual disability 99

OBO ID: DOID:0112026

Term Name:	non-syndromic X-linked intellectual disability 99		Search Ontology:
Synonyms:	MRX99 X-linked mental retardation 99
Definition:	A non-syndromic X-linked intellectual disability characterized by developmental delay, hypotonia, and variable behavioral abnormalities that has_material_basis_in hemizygous mutation in the USP9X gene on chromosome Xp11.4. https://pubmed.ncbi.nlm.nih.gov/24607389/
References:	OMIM:300919
Ontology:	Human Disease ( DOID:0112026 )

Relationships

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

OTHER non-syndromic X-linked intellectual disability 99 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
USP9X	usp9	Intellectual developmental disorder, X-linked 99	300919
USP9Y	usp9	Intellectual developmental disorder, X-linked 99	300919

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None