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DO Term : pontocerebellar hypoplasia type 4 [DOID:0060273] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A pontocerebellar hypoplasia that is characterized by progressive microcephaly, hypertonia, myoclonus, seizure and early lethality, has_material_basis_in autosomal recessive inheritance of mutation in the TSEN54 gene.
  • synonyms:
  • UMLS_CUI:C1856974,
  • ORDO:166063,
  • SNOMEDCT_US_2023_03_01:718608006,
  • GARD:343,
  • OMIM:225753,
  • MESH:C536716,
  • 225753
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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