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Namespace Prefixes

PrefixIRI
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xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_0060273
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0060264
rdfs:label
pontocerebellar hypoplasia type 4
rdfs:comment
NT MGI.
wdrs:describedby
n6:doid.owl
obo:id
DOID:0060273
obo:created_by
emitraka
obo:creation_date
2015-02-04T14:28:28Z
obo:hasDbXref
SNOMEDCT_US_2021_09_01:718608006 OMIM:225753 ORDO:166063 GARD:343 MESH:C536716 UMLS_CUI:C1856974
obo:hasOBONamespace
disease_ontology
obo:inSubset
n7:DO_rare_slim
n2:IAO_0000115
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.