non-syndromic X-linked intellectual disability 58

Summary

DOID:0112024 - non-syndromic X-linked intellectual disability 58

Disease Ontology Definition:A non-syndromic X-linked intellectual disability characterized by mild to moderate intellectual disability and no consistent dysmorphic features that has_material_basis_in hemizygous mutation in the TSPAN7 gene on chromosome Xp11.4.

Synonyms: MRX58, X-linked mental retardation 58

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: tspan7

MIM:

MIM:300210 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 58; XLID58

MIM:300210 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 58; XLID58

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): non-syndromic X-linked intellectual disability (is_a), X-linked recessive disease (is_a)