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Human Disease

pontocerebellar hypoplasia type 4

Term ID
DOID:0060273
Synonyms
Definition
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. https://www.omim.org/entry/225753
References
  • GARD:343
  • MESH:C536716
  • MIM:225753
  • ORDO:166063
  • SNOMEDCT_US_2023_03_01:718608006
  • UMLS_CUI:C1856974
Ontology
Human Disease   ( DOID:0060273 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations