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DO Term : developmental delay, hypotrophy, and dysmorphic features without Moebius syndrome [DOID:0081264] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A syndrome that is characterized by developmental delay, hypotrophy, and dysmorphic features and that has_material_basis_in homozygous ultra-rare REV3L variant (T2753R).

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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