|  Help  |  About  |  Contact Us

DO Term : pontocerebellar hypoplasia type 2A [DOID:0060267] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A severe pontocerebellar hypoplasia that is characterized by progressive microcephaly, chorea, epilepsy and hyperreflexia, has_material_basis_in autosomal recessive inheritance of mutation in the TSEN54 gene.
  • synonyms:
  • GARD:10705,
  • MESH:C564738,
  • OMIM:277470,
  • ORDO:2524,
  • GARD:3631,
  • UMLS_CUI:C1848526,
  • 277470
Quick Links:
 
Quick Links:
 

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