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DO Term : syndromic X-linked intellectual disability Raymond type [DOID:0060824] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A syndromic X-linked intellectual disability characterized by intellectual disability and marfanoid habitus that has_material_basis_in mutation in the ZDHHC9 gene on chromosome Xq26.1.

synonyms:
ORDO:163953,
X-linked syndromic intellectual developmental disorder Raymond type,
300799,
mental retardation, X-linked syndromic, Raymond type,
MRXSR,
OMIM:300799,
ICD10CM:Q87.8

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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