About: pontocerebellar hypoplasia type 1C

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal recessive disease pontocerebellar hypoplasia type 1 nodeID://b50946519
label	pontocerebellar hypoplasia type 1C
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0112334
database_cross_reference	OMIM:616081
has_exact_synonym	PCH1C
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A pontocerebellar hypoplasia type 1 characterized by severe muscle weakness and failure to thrive apparent in the first months of life that has_material_basis_in homozygous or compound heterozygous mutation in EXOSC8 on chromosome 13q13.3.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50946520

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