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DO Term : Joubert syndrome 10 [DOID:0110981] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Joubert syndrome that has_material_basis_in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.

synonyms:
JBTS10,
300804,
OMIM:300804,
MESH:C567582

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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