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About:
pontocerebellar hypoplasia type 10
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
NT MGI.
Attributes
Values
type
Class
subClassOf
pontocerebellar hypoplasia
label
pontocerebellar hypoplasia type 10
comment
NT MGI.
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0060279
created_by
emitraka
creation_date
2015-02-04T14:28:28Z
database_cross_reference
OMIM:615803
ORDO:411493
has_obo_namespace
disease_ontology
in_subset
DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115
A pontocerebellar hypoplasia that is characterized by severe developmental delays, progressive microcephaly, spasticity and seizure, has_material_basis_in autosomal recessive inheritance of mutation in the CLP1 gene.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50938584
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