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DO Term : non-syndromic X-linked intellectual disability 21 [DOID:0112022] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
X-linked mental retardation 21/34,
MRX21,
X-linked mental retardation 21,
MRX34,
OMIM:300143,
X-linked mental retardation 34,
300143

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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