ZFIN Human Disease: non-syndromic X-linked intellectual disability 21

OBO ID: DOID:0112022

Term Name:	non-syndromic X-linked intellectual disability 21		Search Ontology:
Synonyms:	MRX21 MRX34 X-linked mental retardation 21 X-linked mental retardation 21/34 X-linked mental retardation 34
Definition:	A non-syndromic X-linked intellectual disability characterized by a spectrum of cognitive neurologic impairments ranging from moderate mental retardation to high-functioning autism that has_material_basis_in hemizygous mutation in the IL1RAPL1 gene on chromosome Xp21.3-p21.2. https://pubmed.ncbi.nlm.nih.gov/18801879/
References:	OMIM:300143
Ontology:	Human Disease ( DOID:0112022 )

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 21 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
IL1RAPL1	il1rapl1a il1rapl1b	Intellectual developmental disorder, X-linked 21	300143

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None