ZFIN Human Disease: non-syndromic X-linked intellectual disability 91

OBO ID: DOID:0112043

OBO ID: DOID:0112043

Term Name:	non-syndromic X-linked intellectual disability 91	Search Ontology:
Synonyms:	MRX91 X-linked mental retardation 91
Definition:	A non-syndromic X-linked intellectual disability characterized by severe intellectual disability that has_material_basis_in heterozygous mutation in a region on chromosome Xq13.3. https://pubmed.ncbi.nlm.nih.gov/15915161/
References:	OMIM:300577
Ontology:	Human Disease ( DOID:0112043 )

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 91 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None