ZFIN Human Disease: non-syndromic X-linked intellectual disability 53

OBO ID: DOID:0112047

OBO ID: DOID:0112047

Term Name:	non-syndromic X-linked intellectual disability 53	Search Ontology:
Synonyms:	MRX53 X-linked mental retardation 53
Definition:	A non-syndromic X-linked intellectual disability that has_material_basis_in hemizygous mutation in a region on chromosome Xq22.2-q26. https://pubmed.ncbi.nlm.nih.gov/11337751/
References:	OMIM:300324
Ontology:	Human Disease ( DOID:0112047 )

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 53 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None