ZFIN Human Disease: non-syndromic X-linked intellectual disability 103

OBO ID: DOID:0112020

Term Name:	non-syndromic X-linked intellectual disability 103		Search Ontology:
Synonyms:	MRX103 X-linked mental retardation 103
Definition:	A non-syndromic X-linked intellectual disability characterized by intellectual disability and facial feature anomalies that has_material_basis_in hemizygous mutation in the KLHL15 gene on chromosome Xp22.11. (2)
References:	OMIM:300982
Ontology:	Human Disease ( DOID:0112020 )

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 103 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
KLHL15	klhl15	Intellectual developmental disorder, X-linked 103	300982

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None