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DO Term : Armfield syndrome [DOID:0050764] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A syndromic X-linked intellectual disability characterized by intellectual disability, short stature, seizures, and small hands and feet and in some cases cleft palate or cataracts/glaucoma that has_material_basis_in variation in the chromosomal region Xq28.

synonyms:
MRXSA,
OMIM:300261,
mental retardation syndrome, X-linked, Armfield type,
ICD10CM:Q87.8,
Armfield X-linked mental retardation syndrome,
ORDO:85276,
syndromic X-linked mental retardation Armfield type,
X-linked intellectual disability, Armfield type,
300261

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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