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DO Term : pontocerebellar hypoplasia type 7 [DOID:0060276] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A pontocerebellar hypoplasia that is characterized by delayed psychomotor development, hypotonia, gonadal abnormalities and respiratory failure, has_material_basis_in autosomal recessive mutation in the TOE1 gene.
  • synonyms:
  • OMIM:614969,
  • ORDO:284339,
  • 614969,
  • ICD10CM:Q04.3
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents