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DO Term : non-syndromic X-linked intellectual disability 9 [DOID:0112034] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A non-syndromic X-linked intellectual disability characterized by nonprogressive intellectual disability that has_material_basis_in hemizygous mutation in the FTSJ1 gene on chromosome Xp11.23.

synonyms:
OMIM:309549,
MRX9,
X-linked mental retardation 9,
X-linked mental retardation 44,
309549,
MRX44

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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